Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 83692 |
|---|---|
| ensemblid | ENSG00000102181.22 |
| hgncid | 18237 |
| symbol | CD99L2 |
| name | CD99 molecule like 2 |
| refseq_nuc | NM_031462.4 |
| refseq_prot | NP_113650.2 |
| ensembl_nuc | ENST00000370377.8 |
| ensembl_prot | ENSP00000359403.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 150766336 |
| end | 150898668 |
| strand | - |
| ver | v1.2 |
| region | chrX:150766336-150898668 |
| region5000 | chrX:150761336-150903668 |
| regionname0 | CD99L2_chrX_150766336_150898668 |
| regionname5000 | CD99L2_chrX_150761336_150903668 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 262 | 210 | 61 | 34 | 78 | 13 | 22 | 59 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0002 | 0/0 | 262 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0003 | 0/0 | 235 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 789 | 201 | 56 | 34 | 74 | 13 | 22 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| c0002 | 0/0 | 789 | 8 | 4 | 0 | 4 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| c0003 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| c0004 | 0/0 | 787 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| c0005 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2779 | 94 | 12 | 15 | 57 | 4 | 5 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0002 | 0/0 | 2779 | 21 | 3 | 10 | 4 | 2 | 2 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0003 | 0/0 | 2779 | 11 | 0 | 0 | 6 | 0 | 5 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0004 | 0/1 | 2779 | 10 | 1 | 2 | 4 | 0 | 2 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0005 | 0/0 | 2779 | 6 | 5 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0006 | 0/0 | 2779 | 5 | 1 | 1 | 0 | 2 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0007 | 0/0 | 2779 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0008 | 0/0 | 2782 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0009 | 0/0 | 2779 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0010 | 0/0 | 2779 | 4 | 0 | 2 | 0 | 1 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0011 | 0/0 | 2779 | 3 | 3 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0012 | 0/0 | 2779 | 3 | 3 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0013 | 0/0 | 2779 | 3 | 0 | 0 | 0 | 0 | 3 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0014 | 0/0 | 2782 | 3 | 3 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0015 | 0/0 | 2779 | 2 | 0 | 1 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0016 | 0/0 | 2779 | 2 | 2 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0017 | 0/0 | 2782 | 2 | 2 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0018 | 0/0 | 2779 | 2 | 0 | 0 | 2 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0019 | 0/0 | 2779 | 2 | 1 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0020 | 0/0 | 2779 | 2 | 0 | 0 | 2 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0021 | 0/0 | 2779 | 2 | 0 | 0 | 0 | 2 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0022 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0023 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0024 | 0/0 | 2782 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0025 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0026 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0027 | 0/0 | 2779 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0028 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0029 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0030 | 0/0 | 2779 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0031 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0032 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0033 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0034 | 0/0 | 2780 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0035 | 0/0 | 2782 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0036 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0037 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0038 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0039 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0040 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0041 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0042 | 0/0 | 2779 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0043 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| t0044 | 0/0 | 2782 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 789 | 201 | 56 | 34 | 74 | 13 | 22 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0002 | 0/0 | 789 | 8 | 4 | 0 | 4 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0005 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0002c0003 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0003c0004 | 0/0 | 787 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3567 | 87 | 8 | 15 | 54 | 4 | 5 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0002 | 0/0 | 3567 | 20 | 2 | 10 | 4 | 2 | 2 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0003 | 0/0 | 3567 | 11 | 0 | 0 | 6 | 0 | 5 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0004 | 0/1 | 3567 | 10 | 1 | 2 | 4 | 0 | 2 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0005 | 0/0 | 3567 | 6 | 5 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0006 | 0/0 | 3567 | 5 | 1 | 1 | 0 | 2 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0007 | 0/0 | 3567 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0008 | 0/0 | 3570 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0009 | 0/0 | 3567 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0010 | 0/0 | 3567 | 4 | 0 | 2 | 0 | 1 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0011 | 0/0 | 3567 | 3 | 3 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0012 | 0/0 | 3567 | 2 | 2 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0013 | 0/0 | 3567 | 3 | 0 | 0 | 0 | 0 | 3 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0014 | 0/0 | 3570 | 3 | 3 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0015 | 0/0 | 3567 | 2 | 0 | 1 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0016 | 0/0 | 3567 | 2 | 2 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0017 | 0/0 | 3570 | 2 | 2 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0018 | 0/0 | 3567 | 2 | 0 | 0 | 2 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0019 | 0/0 | 3567 | 2 | 1 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0020 | 0/0 | 3567 | 2 | 0 | 0 | 2 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0021 | 0/0 | 3567 | 2 | 0 | 0 | 0 | 2 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0023 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0024 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0025 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0026 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0027 | 0/0 | 3567 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0028 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0029 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0030 | 0/0 | 3567 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0031 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0032 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0033 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0034 | 0/0 | 3568 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0035 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0036 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0037 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0038 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0039 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0040 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0041 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0043 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0001t0044 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0002t0001 | 0/0 | 3567 | 6 | 3 | 0 | 3 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0002t0002 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0002t0022 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0001c0005t0001 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0002c0003t0012 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| a0003c0004t0042 | 0/0 | 3565 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | copy fasta | chrX | 150761336 | 150903668 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0010g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0011g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0012g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0013g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0013g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0013g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0014g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0015g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0015g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0017g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0017g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0018g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0018g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0019g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0019g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0020g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0020g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0021g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0021g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0023g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0024g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0025g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0026g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0027g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0028g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0029g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0030g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0031g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0032g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0033g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0034g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0035g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0036g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0037g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0038g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0039g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0040g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0041g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0043g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0044g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0022g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0002c0003t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0003c0004t0042g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0185 | EUR | GBR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0082 | EUR | GBR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00323 | hp1 | a0001 | c0001 | t0015 | g0128 | EUR | FIN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00438 | hp2 | a0001 | c0001 | t0041 | g0208 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00673 | hp1 | a0001 | c0002 | t0022 | g0100 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0179 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01168 | hp1 | a0001 | c0001 | t0010 | g0019 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01168 | hp2 | a0003 | c0004 | t0042 | g0209 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01243 | hp1 | a0001 | c0001 | t0044 | g0210 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0133 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01496 | hp2 | a0001 | c0001 | t0015 | g0135 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01515 | hp1 | a0001 | c0001 | t0021 | g0117 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0137 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01516 | hp2 | a0001 | c0001 | t0027 | g0151 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0138 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01517 | hp2 | a0001 | c0001 | t0021 | g0150 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0163 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01934 | hp1 | a0001 | c0001 | t0035 | g0167 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0172 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02257 | hp2 | a0001 | c0001 | t0024 | g0190 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02280 | hp1 | a0001 | c0001 | t0037 | g0143 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0169 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0164 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02615 | hp2 | a0002 | c0003 | t0012 | g0166 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02630 | hp1 | a0001 | c0001 | t0028 | g0074 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0194 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0189 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0177 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02886 | hp1 | a0001 | c0001 | t0025 | g0144 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0130 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02895 | hp1 | a0001 | c0001 | t0023 | g0005 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0073 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0020 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03041 | hp1 | a0001 | c0001 | t0026 | g0149 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0142 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03098 | hp1 | a0001 | c0001 | t0039 | g0170 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0207 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03209 | hp1 | a0001 | c0001 | t0036 | g0145 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03225 | hp1 | a0001 | c0001 | t0029 | g0116 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0046 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0195 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0160 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03540 | hp1 | a0001 | c0001 | t0031 | g0158 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0147 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0072 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03654 | hp1 | a0001 | c0001 | t0030 | g0045 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0038 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03688 | hp1 | a0001 | c0001 | t0034 | g0028 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0199 | SAS | BEB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03942 | hp1 | a0001 | c0001 | t0019 | g0178 | SAS | BEB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG04115 | hp1 | a0001 | c0001 | t0013 | g0078 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0052 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0161 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0171 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18906 | hp2 | a0001 | c0001 | t0033 | g0148 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18945 | hp1 | a0001 | c0001 | t0018 | g0104 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18960 | hp1 | a0001 | c0001 | t0018 | g0105 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18979 | hp1 | a0001 | c0001 | t0020 | g0060 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19000 | hp1 | a0001 | c0001 | t0020 | g0025 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0198 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19043 | hp1 | a0001 | c0001 | t0019 | g0174 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19075 | hp1 | a0001 | c0001 | t0040 | g0006 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19240 | hp1 | a0001 | c0001 | t0043 | g0211 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0180 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20129 | hp1 | a0001 | c0001 | t0032 | g0182 | AFR | ASW | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | ASW | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0095 | EUR | TSI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20905 | hp1 | a0001 | c0001 | t0013 | g0071 | SAS | GIH | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02559 | hp1 | a0001 | c0001 | t0038 | g0136 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0191 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0197 | AFR | USA | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | USA | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0146 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0088 | REF | REF | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| 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:150770304
|
C | T | 1 | a0003 | 1 | HG01168.hp2 | missense_variant&splice_region_variant | MODERATE | c.721G>A | p.Val241Met | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/11 | 801/3567 | 721/789 | 241/262 | chrX | 150770304 | ||
| chrX:150770305
|
T | G | 1 | a0003 | 1 | HG01168.hp2 | missense_variant&splice_region_variant | MODERATE | c.720A>C | p.Gln240His | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/11 | 800/3567 | 720/789 | 240/262 | chrX | 150770305 | ||
| chrX:150770306
|
T | A | 1 | a0003 | 1 | HG01168.hp2 | missense_variant&splice_region_variant | MODERATE | c.719A>T | p.Gln240Leu | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/11 | 799/3567 | 719/789 | 240/262 | chrX | 150770306 | ||
| chrX:150776179
|
AT | A | 1 | a0003 | 1 | HG01168.hp2 | frameshift_variant | HIGH | c.649delA | p.Ile217fs | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/11 | 729/3567 | 649/789 | 217/262 | chrX | 150776179 | ||
| chrX:150776292
|
GC | G | 1 | a0003 | 1 | HG01168.hp2 | frameshift_variant&splice_region_variant | HIGH | c.536delG | p.Gly179fs | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/11 | 616/3567 | 536/789 | 179/262 | chrX | 150776292 | ||
| chrX:150777449
|
C | T | 1 | a0002 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.530G>A | p.Gly177Glu | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/11 | 610/3567 | 530/789 | 177/262 | chrX | 150777449 |
| 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:150769055
|
C | T | 2 | a0001c0002a0001c0005 | 9 | HG00438.hp1 HG00673.hp1 HG02109.hp2 others(6): Show |
synonymous_variant | LOW | c.768G>A | p.Pro256Pro | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 848/3567 | 768/789 | 256/262 | chrX | 150769055 | ||
| chrX:150769088
|
C | T | 1 | a0001c0005 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.735G>A | p.Thr245Thr | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 815/3567 | 735/789 | 245/262 | chrX | 150769088 |
| 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:150766542
|
GC | G | 1 | a0001c0001t0040 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2491delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 2491 | chrX | 150766542 | |||||
| chrX:150766592
|
A | AGTT | 6 | a0001c0001t0008a0001c0001t0014a0001c0001t0017others(3): Show | 12 | HG01243.hp1 HG01934.hp1 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2439_*2441dupAAC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 2441 | chrX | 150766592 | |||||
| chrX:150766627
|
T | C | 25 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(22): Show | 82 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2407A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 2407 | chrX | 150766627 | |||||
| chrX:150766875
|
C | T | 1 | a0001c0001t0016 | 2 | HG02896.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2159G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 2159 | chrX | 150766875 | |||||
| chrX:150766915
|
G | GC | 1 | a0001c0001t0040 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 2118 | chrX | 150766915 | |||||
| chrX:150766925
|
C | CG | 1 | a0001c0001t0034 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2108dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 2108 | chrX | 150766925 | |||||
| chrX:150766940
|
G | T | 1 | a0001c0001t0030 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2094C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 2094 | chrX | 150766940 | |||||
| chrX:150767050
|
G | A | 1 | a0001c0001t0010 | 4 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1984C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 1984 | chrX | 150767050 | |||||
| chrX:150767381
|
G | C | 2 | a0001c0001t0011a0001c0001t0026 | 4 | HG01884.hp2 HG02615.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1653C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 1653 | chrX | 150767381 | |||||
| chrX:150767493
|
G | T | 1 | a0001c0001t0039 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 1541 | chrX | 150767493 | |||||
| chrX:150767547
|
A | C | 1 | a0001c0001t0036 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1487T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 1487 | chrX | 150767547 | |||||
| chrX:150767607
|
TC | T | 1 | a0001c0001t0040 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1426delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 1426 | chrX | 150767607 | |||||
| chrX:150767630
|
C | A | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(11): Show | 49 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1404G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 1404 | chrX | 150767630 | |||||
| chrX:150767948
|
T | A | 1 | a0001c0001t0028 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1086A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 1086 | chrX | 150767948 | |||||
| chrX:150768085
|
T | TC | 1 | a0001c0001t0040 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*948dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 948 | chrX | 150768085 | |||||
| chrX:150768198
|
G | A | 1 | a0001c0001t0035 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 836 | chrX | 150768198 | |||||
| chrX:150768240
|
A | G | 5 | a0001c0001t0014a0001c0001t0028a0001c0001t0032others(2): Show | 7 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*794T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 794 | chrX | 150768240 | |||||
| chrX:150768275
|
C | G | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(12): Show | 53 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*759G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 759 | chrX | 150768275 | |||||
| chrX:150768315
|
C | G | 1 | a0001c0001t0024 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*719G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 719 | chrX | 150768315 | |||||
| chrX:150768405
|
T | C | 1 | a0001c0001t0026 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*629A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 629 | chrX | 150768405 | |||||
| chrX:150768424
|
C | G | 2 | a0001c0001t0007a0001c0001t0043 | 5 | HG02145.hp1 HG02280.hp2 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*610G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 610 | chrX | 150768424 | |||||
| chrX:150768482
|
A | G | 1 | a0001c0001t0031 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 552 | chrX | 150768482 | |||||
| chrX:150768498
|
C | T | 5 | a0001c0001t0003a0001c0001t0018a0001c0001t0021others(2): Show | 17 | HG01515.hp1 HG01517.hp2 HG02074.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 536 | chrX | 150768498 | |||||
| chrX:150768525
|
C | G | 4 | a0001c0001t0012a0001c0001t0028a0001c0001t0029others(1): Show | 5 | HG02615.hp2 HG02630.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*509G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 509 | chrX | 150768525 | |||||
| chrX:150768573
|
C | T | 1 | a0001c0001t0027 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 461 | chrX | 150768573 | |||||
| chrX:150768753
|
A | G | 6 | a0001c0001t0011a0001c0001t0024a0001c0001t0025others(3): Show | 8 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*281T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 281 | chrX | 150768753 | |||||
| chrX:150768853
|
C | T | 1 | a0001c0001t0023 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 181 | chrX | 150768853 | |||||
| chrX:150768857
|
TG | T | 1 | a0001c0001t0040 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 176 | chrX | 150768857 | |||||
| chrX:150768903
|
C | T | 1 | a0001c0002t0022 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 131 | chrX | 150768903 | |||||
| chrX:150768916
|
C | G | 4 | a0001c0001t0007a0001c0001t0016a0001c0001t0017others(1): Show | 9 | HG02145.hp1 HG02280.hp2 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*118G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 118 | chrX | 150768916 | |||||
| chrX:150768931
|
T | C | 9 | a0001c0001t0005a0001c0001t0006a0001c0001t0009others(6): Show | 25 | HG00099.hp1 HG00140.hp1 HG01081.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*103A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 103 | chrX | 150768931 | |||||
| chrX:150768955
|
C | T | 1 | a0001c0001t0015 | 2 | HG00323.hp1 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*79G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 79 | chrX | 150768955 | |||||
| chrX:150768958
|
G | GGT | 1 | a0001c0001t0040 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*75_*76insAC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 75 | chrX | 150768958 | |||||
| chrX:150768959
|
T | C | 1 | a0001c0001t0040 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*75A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 75 | chrX | 150768959 | |||||
| chrX:150768968
|
AG | A | 1 | a0001c0001t0040 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*65delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 11/11 | 65 | chrX | 150768968 | |||||
| chrX:150898619
|
G | C | 1 | a0001c0001t0041 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-31C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/11 | 31 | chrX | 150898619 | |||||
| chrX:150898626
|
T | G | 1 | a0003c0004t0042 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/11 | 38 | chrX | 150898626 | |||||
| chrX:150898638
|
G | A | 2 | a0001c0001t0043a0001c0001t0044 | 2 | HG01243.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-50C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/11 | 50 | chrX | 150898638 |
| 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:150769145
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0002g0112 | 2 | HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.722-44C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769145 | ||||||
| chrX:150769357
|
G | A | 25 | a0001c0001t0001g0080a0001c0001t0001g0111a0001c0001t0001g0193others(22): Show | 25 | HG00140.hp1 HG00280.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.722-256C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769357 | ||||||
| chrX:150769364
|
G | A | 1 | a0001c0001t0014g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.722-263C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769364 | ||||||
| chrX:150769568
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.722-467A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769568 | ||||||
| chrX:150769592
|
TCCTGGTC others(108): Show |
T | 1 | a0001c0001t0010g0179 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.721+597_722-492del | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769592 | ||||||
| chrX:150769651
|
CGCCTGAG others(16): Show |
C | 1 | a0001c0001t0015g0128 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.722-573_722-551del others(23): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769651 | ||||||
| chrX:150769653
|
CCTGAGCT others(35): Show |
C | 1 | a0001c0001t0009g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.722-594_722-553del others(42): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769653 | ||||||
| chrX:150769673
|
CTGCCTGC others(7): Show |
C | 3 | a0001c0001t0017g0020a0001c0001t0017g0194a0001c0002t0001g0173 | 3 | HG02647.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.722-586_722-573del others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769673 | ||||||
| chrX:150769674
|
TGCCTGCG others(7): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.722-587_722-574del others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769674 | ||||||
| chrX:150769674
|
TGCCTGCG others(106): Show |
T | 22 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0132others(19): Show | 22 | HG00408.hp1 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.721+517_722-574del | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769674 | ||||||
| chrX:150769677
|
C | A | 9 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | NA18612.hp1 NA18961.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.722-576G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769677 | ||||||
| chrX:150769678
|
T | G | 9 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | NA18612.hp1 NA18961.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.722-577A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769678 | ||||||
| chrX:150769680
|
C | G | 9 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | NA18612.hp1 NA18961.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.722-579G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769680 | ||||||
| chrX:150769681
|
GCCACCAG others(130): Show |
G | 9 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | NA18612.hp1 NA18961.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.721+486_722-581del | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769681 | ||||||
| chrX:150769684
|
ACCAGGCC others(17): Show |
A | 8 | a0001c0001t0001g0162a0001c0001t0002g0017a0001c0001t0004g0176others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.721+596_722-584del others(24): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769684 | ||||||
| chrX:150769688
|
G | A | 3 | a0001c0001t0017g0020a0001c0001t0017g0194a0001c0002t0001g0173 | 3 | HG02647.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.722-587C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769688 | ||||||
| chrX:150769689
|
GCCTCGGC others(10): Show |
G | 40 | a0001c0001t0001g0015a0001c0001t0001g0077a0001c0001t0001g0115others(37): Show | 40 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.721+598_722-589del others(17): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769689 | ||||||
| chrX:150769706
|
AC | A | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.721+597delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769706 | ||||||
| chrX:150769746
|
TG | T | 1 | a0001c0001t0001g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.721+557delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769746 | ||||||
| chrX:150769752
|
CAGG | C | 1 | a0001c0001t0001g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.721+549_721+551del others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769752 | ||||||
| chrX:150769761
|
T | C | 50 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0077others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.721+543A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769761 | ||||||
| chrX:150769819
|
T | A | 9 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | NA18612.hp1 NA18961.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.721+485A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769819 | ||||||
| chrX:150769882
|
G | C | 2 | a0001c0002t0001g0009a0001c0002t0022g0100 | 2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.721+422C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769882 | ||||||
| chrX:150769978
|
TG | T | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.721+325delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150769978 | ||||||
| chrX:150770006
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.721+298C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150770006 | ||||||
| chrX:150770042
|
G | A | 3 | a0001c0001t0002g0140a0001c0001t0008g0139a0001c0001t0017g0194 | 3 | HG02630.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.721+262C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150770042 | ||||||
| chrX:150770045
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.721+259G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150770045 | ||||||
| chrX:150770068
|
G | A | 1 | a0001c0001t0013g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.721+236C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150770068 | ||||||
| chrX:150770189
|
G | A | 6 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0007g0196others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.721+115C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 10/10 | chrX | 150770189 | ||||||
| chrX:150770424
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-55T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150770424 | ||||||
| chrX:150770429
|
G | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(13): Show | 16 | HG00438.hp1 HG00673.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.656-60C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150770429 | ||||||
| chrX:150770608
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.656-239G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150770608 | ||||||
| chrX:150770754
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0206 | 2 | NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.656-385A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150770754 | ||||||
| chrX:150770793
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0155 | 2 | HG02040.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.656-424C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150770793 | ||||||
| chrX:150770835
|
C | A | 14 | a0001c0001t0001g0083a0001c0001t0001g0165a0001c0001t0001g0184others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.656-466G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150770835 | ||||||
| chrX:150770864
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.656-495G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150770864 | ||||||
| chrX:150770869
|
C | A | 14 | a0001c0001t0001g0083a0001c0001t0001g0184a0001c0001t0001g0186others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.656-500G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150770869 | ||||||
| chrX:150771041
|
C | T | 1 | a0001c0001t0028g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.656-672G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771041 | ||||||
| chrX:150771044
|
G | C | 1 | a0001c0001t0008g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-675C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771044 | ||||||
| chrX:150771052
|
G | C | 1 | a0001c0001t0008g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-683C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771052 | ||||||
| chrX:150771059
|
G | A | 12 | a0001c0001t0005g0141a0001c0001t0007g0196a0001c0001t0007g0197others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.656-690C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771059 | ||||||
| chrX:150771149
|
G | A | 49 | a0001c0001t0001g0069a0001c0001t0001g0077a0001c0001t0001g0084others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.656-780C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771149 | ||||||
| chrX:150771155
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.656-786C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771155 | ||||||
| chrX:150771188
|
A | AC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.656-820dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771188 | ||||||
| chrX:150771191
|
G | GA | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.656-823dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771191 | ||||||
| chrX:150771192
|
A | AG | 1 | a0001c0001t0001g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.656-824_656-823ins others(1): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771192 | ||||||
| chrX:150771224
|
G | A | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.656-855C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771224 | ||||||
| chrX:150771228
|
T | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0041others(20): Show | 23 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.656-859A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771228 | ||||||
| chrX:150771279
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0053 | 2 | HG02056.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.656-910C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771279 | ||||||
| chrX:150771317
|
G | A | 1 | a0001c0001t0036g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.656-948C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771317 | ||||||
| chrX:150771355
|
G | A | 2 | a0001c0001t0007g0204a0001c0001t0033g0148 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.656-986C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771355 | ||||||
| chrX:150771370
|
G | A | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.656-1001C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771370 | ||||||
| chrX:150771684
|
G | A | 1 | a0001c0001t0009g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.656-1315C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771684 | ||||||
| chrX:150771687
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.656-1318C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771687 | ||||||
| chrX:150771885
|
G | A | 1 | a0001c0001t0027g0151 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.656-1516C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771885 | ||||||
| chrX:150772195
|
T | A | 1 | a0001c0001t0027g0151 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.656-1826A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150772195 | ||||||
| chrX:150772215
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.656-1846G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150772215 | ||||||
| chrX:150772304
|
G | A | 1 | a0001c0001t0023g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.656-1935C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150772304 | ||||||
| chrX:150772314
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.656-1945G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150772314 | ||||||
| chrX:150772465
|
G | A | 9 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0007g0196others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.656-2096C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150772465 | ||||||
| chrX:150772565
|
C | T | 1 | a0001c0001t0005g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.656-2196G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150772565 | ||||||
| chrX:150772605
|
T | TA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.656-2237dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150772605 | ||||||
| chrX:150773042
|
AT | A | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.656-2674delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150773042 | ||||||
| chrX:150773251
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 135 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.656-2882A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150773251 | ||||||
| chrX:150773543
|
G | C | 1 | a0001c0002t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655+2631C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150773543 | ||||||
| chrX:150773569
|
C | T | 14 | a0001c0001t0001g0083a0001c0001t0001g0165a0001c0001t0001g0184others(11): Show | 14 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.655+2605G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150773569 | ||||||
| chrX:150773679
|
A | C | 3 | a0001c0001t0016g0072a0001c0001t0016g0073a0001c0001t0017g0020 | 3 | HG02896.hp2 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.655+2495T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150773679 | ||||||
| chrX:150773762
|
A | G | 14 | a0001c0001t0005g0141a0001c0001t0005g0202a0001c0001t0005g0203others(11): Show | 14 | HG01934.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.655+2412T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150773762 | ||||||
| chrX:150773955
|
G | C | 6 | a0001c0001t0005g0141a0001c0001t0005g0202a0001c0001t0005g0203others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+2219C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150773955 | ||||||
| chrX:150773965
|
AG | A | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.655+2208delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150773965 | ||||||
| chrX:150774145
|
AT | A | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.655+2028delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774145 | ||||||
| chrX:150774149
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.655+2025C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774149 | ||||||
| chrX:150774254
|
TG | T | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.655+1919delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774254 | ||||||
| chrX:150774327
|
G | A | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.655+1847C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774327 | ||||||
| chrX:150774373
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.655+1801C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774373 | ||||||
| chrX:150774381
|
T | TC | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.655+1792dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774381 | ||||||
| chrX:150774410
|
C | T | 10 | a0001c0001t0001g0031a0001c0001t0001g0048a0001c0001t0001g0057others(7): Show | 10 | NA18612.hp1 NA18961.hp1 NA18979.hp1 others(7): Show |
intron_variant | MODIFIER | c.655+1764G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774410 | ||||||
| chrX:150774535
|
G | A | 39 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0110others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.655+1639C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774535 | ||||||
| chrX:150774590
|
G | A | 3 | a0001c0001t0001g0041a0001c0002t0001g0009a0001c0002t0022g0100 | 3 | HG00438.hp1 HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.655+1584C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774590 | ||||||
| chrX:150774703
|
CA | C | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+1470delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774703 | ||||||
| chrX:150774710
|
T | TC | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.655+1463dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774710 | ||||||
| chrX:150774714
|
C | T | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.655+1460G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774714 | ||||||
| chrX:150774732
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.655+1442G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774732 | ||||||
| chrX:150774857
|
TA | T | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+1316delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774857 | ||||||
| chrX:150774956
|
T | TC | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+1217dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774956 | ||||||
| chrX:150775112
|
T | TG | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+1061dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775112 | ||||||
| chrX:150775257
|
C | CG | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+916dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775257 | ||||||
| chrX:150775314
|
GA | G | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+859delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775314 | ||||||
| chrX:150775322
|
C | CCA | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+850_655+851dup others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775322 | ||||||
| chrX:150775342
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.655+832G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775342 | ||||||
| chrX:150775391
|
G | A | 1 | a0001c0001t0004g0176 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.655+783C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775391 | ||||||
| chrX:150775449
|
GC | G | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+724delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775449 | ||||||
| chrX:150775536
|
G | GT | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+637dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775536 | ||||||
| chrX:150775557
|
GGGT | G | 2 | a0001c0001t0003g0085a0001c0001t0030g0045 | 2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.655+614_655+616del others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775557 | ||||||
| chrX:150775571
|
G | T | 1 | a0001c0001t0044g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.655+603C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775571 | ||||||
| chrX:150775651
|
G | C | 63 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0059others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.655+523C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775651 | ||||||
| chrX:150775727
|
AC | A | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+446delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775727 | ||||||
| chrX:150775852
|
G | T | 1 | a0001c0001t0033g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.655+322C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775852 | ||||||
| chrX:150775857
|
TC | T | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+316delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775857 | ||||||
| chrX:150775861
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.655+313T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775861 | ||||||
| chrX:150775868
|
G | A | 5 | a0001c0001t0001g0132a0001c0001t0002g0027a0001c0001t0002g0087others(2): Show | 5 | HG01074.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+306C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775868 | ||||||
| chrX:150775945
|
A | C | 2 | a0001c0001t0004g0176a0001c0001t0026g0149 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.655+229T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775945 | ||||||
| chrX:150775957
|
C | A | 2 | a0001c0001t0005g0202a0001c0001t0005g0203 | 2 | HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.655+217G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775957 | ||||||
| chrX:150776038
|
TCCACCC | T | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.655+130_655+135del others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150776038 | ||||||
| chrX:150776041
|
A | ACC | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+131_655+132dup others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150776041 | ||||||
| chrX:150776098
|
T | TG | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+75dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150776098 | ||||||
| chrX:150776157
|
T | TG | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.655+16dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150776157 | ||||||
| chrX:150776305
|
A | AG | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.536-13dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776305 | ||||||
| chrX:150776360
|
TG | T | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.536-68delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776360 | ||||||
| chrX:150776368
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.536-75A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776368 | ||||||
| chrX:150776410
|
C | T | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.536-117G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776410 | ||||||
| chrX:150776454
|
CA | C | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.536-162delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776454 | ||||||
| chrX:150776642
|
A | AC | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.536-350dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776642 | ||||||
| chrX:150776719
|
C | G | 12 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0069others(9): Show | 12 | HG01258.hp1 HG01261.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.536-426G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776719 | ||||||
| chrX:150776786
|
GC | G | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.536-494delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776786 | ||||||
| chrX:150776877
|
C | CG | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.535+566dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776877 | ||||||
| chrX:150776947
|
CA | C | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.535+496delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776947 | ||||||
| chrX:150776963
|
G | C | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.535+481C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776963 | ||||||
| chrX:150776964
|
T | G | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.535+480A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776964 | ||||||
| chrX:150776965
|
G | T | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.535+479C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776965 | ||||||
| chrX:150776976
|
A | T | 1 | a0001c0001t0008g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.535+468T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776976 | ||||||
| chrX:150777012
|
G | GC | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.535+431dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150777012 | ||||||
| chrX:150777079
|
A | AT | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.535+364dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150777079 | ||||||
| chrX:150777242
|
G | A | 2 | a0001c0001t0004g0176a0001c0001t0026g0149 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.535+202C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150777242 | ||||||
| chrX:150777322
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.535+122C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150777322 | ||||||
| chrX:150777515
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.497-33C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150777515 | ||||||
| chrX:150777522
|
C | CAGCTCAG others(5): Show |
5 | a0001c0001t0001g0132a0001c0001t0002g0027a0001c0001t0002g0087others(2): Show | 5 | HG01074.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-52_497-41dupCG others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150777522 | ||||||
| chrX:150777558
|
T | C | 2 | a0001c0001t0004g0064a0001c0001t0006g0044 | 2 | HG01081.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.497-76A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150777558 | ||||||
| chrX:150777598
|
C | T | 2 | a0001c0002t0001g0201a0002c0003t0012g0166 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497-116G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150777598 | ||||||
| chrX:150778212
|
C | G | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-730G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778212 | ||||||
| chrX:150778339
|
G | A | 1 | a0001c0001t0004g0122 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.497-857C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778339 | ||||||
| chrX:150778342
|
G | A | 1 | a0001c0001t0006g0082 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.497-860C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778342 | ||||||
| chrX:150778401
|
C | A | 3 | a0001c0001t0001g0162a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02055.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.497-919G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778401 | ||||||
| chrX:150778464
|
T | TG | 1 | a0001c0001t0025g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.497-983dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778464 | ||||||
| chrX:150778508
|
G | A | 2 | a0001c0001t0016g0072a0001c0001t0016g0073 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.497-1026C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778508 | ||||||
| chrX:150778537
|
CCTCT | C | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.497-1059_497-1056d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778537 | ||||||
| chrX:150778576
|
A | G | 11 | a0001c0001t0001g0077a0001c0001t0001g0115a0001c0001t0005g0141others(8): Show | 11 | HG00735.hp2 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-1094T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778576 | ||||||
| chrX:150778673
|
T | TA | 4 | a0001c0001t0025g0144a0001c0001t0028g0074a0001c0001t0036g0145others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-1192dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778673 | ||||||
| chrX:150778673
|
TA | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0007g0196others(2): Show | 5 | HG00642.hp1 HG01192.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-1192delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778673 | ||||||
| chrX:150778673
|
TAA | T | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.497-1193_497-1192d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778673 | ||||||
| chrX:150778673
|
TAAA | T | 10 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0162others(7): Show | 10 | HG00408.hp1 HG00408.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1194_497-1192d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778673 | ||||||
| chrX:150778681
|
A | AATAT | 2 | a0001c0001t0005g0202a0001c0002t0001g0201 | 2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.497-1200_497-1199i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778681 | ||||||
| chrX:150778681
|
A | AATATAT | 1 | a0001c0001t0005g0203 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-1200_497-1199i others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778681 | ||||||
| chrX:150778681
|
A | AATATATA others(1): Show |
3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.497-1200_497-1199i others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778681 | ||||||
| chrX:150778682
|
AAAAAT | A | 2 | a0001c0001t0003g0085a0001c0001t0039g0170 | 2 | HG03098.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.497-1205_497-1201d others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778682 | ||||||
| chrX:150778682
|
AAAAATAT | A | 3 | a0001c0001t0010g0185a0001c0002t0001g0181a0001c0005t0001g0130 | 3 | HG00099.hp1 HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.497-1207_497-1201d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778682 | ||||||
| chrX:150778683
|
A | AATAT | 1 | a0001c0001t0035g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.497-1202_497-1201i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778683 | ||||||
| chrX:150778683
|
A | T | 6 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0008g0168others(3): Show | 6 | HG02258.hp1 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-1201T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778683 | ||||||
| chrX:150778683
|
AAAAT | A | 2 | a0001c0001t0001g0193a0001c0001t0044g0210 | 2 | HG01243.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.497-1205_497-1202d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778683 | ||||||
| chrX:150778683
|
AAAATAT | A | 9 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0069others(6): Show | 9 | HG01081.hp1 HG01258.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-1207_497-1202d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778683 | ||||||
| chrX:150778684
|
AAAT | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0002g0016others(1): Show | 4 | HG03486.hp2 NA18969.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-1205_497-1203d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778684 | ||||||
| chrX:150778684
|
AAATAT | A | 4 | a0001c0001t0002g0118a0001c0001t0004g0093a0001c0001t0030g0045others(1): Show | 4 | HG01074.hp1 HG03654.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-1207_497-1203d others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778684 | ||||||
| chrX:150778684
|
AAATATAT | A | 17 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0031others(14): Show | 17 | HG01099.hp1 HG01168.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.497-1209_497-1203d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778684 | ||||||
| chrX:150778685
|
A | AAAT | 3 | a0001c0001t0011g0163a0001c0001t0011g0164a0001c0001t0011g0171 | 3 | HG01884.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.497-1204_497-1203i others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778685 | ||||||
| chrX:150778685
|
A | T | 14 | a0001c0001t0001g0077a0001c0001t0005g0202a0001c0001t0005g0203others(11): Show | 14 | HG00735.hp2 HG01934.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-1203T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778685 | ||||||
| chrX:150778685
|
AAT | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0003g0103others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-1205_497-1204d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778685 | ||||||
| chrX:150778685
|
AATAT | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0175others(8): Show | 11 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-1207_497-1204d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778685 | ||||||
| chrX:150778685
|
AATATAT | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.497-1209_497-1204d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778685 | ||||||
| chrX:150778686
|
AT | A | 1 | a0001c0001t0007g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.497-1205delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778686 | ||||||
| chrX:150778686
|
ATAT | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0114others(8): Show | 11 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-1207_497-1205d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778686 | ||||||
| chrX:150778686
|
ATATATAT | A | 3 | a0001c0001t0013g0038a0001c0001t0013g0071a0001c0001t0023g0005 | 3 | HG02895.hp1 HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.497-1211_497-1205d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778686 | ||||||
| chrX:150778687
|
T | A | 3 | a0001c0001t0025g0144a0001c0001t0036g0145a0001c0001t0037g0143 | 3 | HG02280.hp1 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.497-1205A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778687 | ||||||
| chrX:150778689
|
T | A | 1 | a0001c0001t0003g0103 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.497-1207A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778689 | ||||||
| chrX:150778691
|
T | A | 2 | a0001c0001t0001g0015a0001c0002t0002g0010 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497-1209A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778691 | ||||||
| chrX:150778693
|
T | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0102a0001c0001t0001g0132others(3): Show | 6 | HG01496.hp2 HG01978.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-1211A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778693 | ||||||
| chrX:150778705
|
T | G | 1 | a0001c0001t0004g0052 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.497-1223A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778705 | ||||||
| chrX:150778849
|
C | CA | 1 | a0001c0001t0020g0025 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.497-1368dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778849 | ||||||
| chrX:150778875
|
A | G | 1 | a0001c0001t0004g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.497-1393T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778875 | ||||||
| chrX:150778910
|
AG | A | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.497-1429delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778910 | ||||||
| chrX:150779081
|
C | A | 2 | a0001c0002t0001g0181a0001c0005t0001g0130 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.497-1599G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779081 | ||||||
| chrX:150779245
|
T | TC | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.497-1764dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779245 | ||||||
| chrX:150779310
|
AT | A | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.497-1829delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779310 | ||||||
| chrX:150779331
|
TG | T | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.497-1850delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779331 | ||||||
| chrX:150779383
|
TC | T | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.497-1902delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779383 | ||||||
| chrX:150779548
|
G | A | 1 | a0001c0001t0019g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.497-2066C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779548 | ||||||
| chrX:150779556
|
C | T | 12 | a0001c0001t0001g0165a0001c0001t0001g0184a0001c0001t0001g0186others(9): Show | 12 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.497-2074G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779556 | ||||||
| chrX:150779684
|
A | G | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.497-2202T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779684 | ||||||
| chrX:150779798
|
T | TA | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.497-2317dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150779798 | ||||||
| chrX:150780010
|
G | A | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.497-2528C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150780010 | ||||||
| chrX:150780181
|
T | C | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.497-2699A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150780181 | ||||||
| chrX:150780241
|
T | C | 1 | a0001c0002t0002g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.497-2759A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150780241 | ||||||
| chrX:150780529
|
A | G | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.497-3047T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150780529 | ||||||
| chrX:150780549
|
T | C | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.497-3067A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150780549 | ||||||
| chrX:150780684
|
T | TA | 2 | a0001c0001t0001g0155a0001c0002t0001g0026 | 2 | NA18981.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.497-3203dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150780684 | ||||||
| chrX:150780905
|
G | A | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.497-3423C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150780905 | ||||||
| chrX:150781086
|
CAAAAAGC others(2): Show |
C | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198 | 3 | HG02145.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.497-3613_497-3605d others(11): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150781086 | ||||||
| chrX:150781294
|
A | G | 1 | a0001c0001t0008g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.497-3812T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150781294 | ||||||
| chrX:150781295
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.497-3813A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150781295 | ||||||
| chrX:150781324
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.497-3842C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150781324 | ||||||
| chrX:150781499
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0008g0161 | 3 | HG01884.hp1 HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.497-4017G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150781499 | ||||||
| chrX:150781932
|
A | C | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.497-4450T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150781932 | ||||||
| chrX:150782171
|
T | C | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-4689A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782171 | ||||||
| chrX:150782177
|
A | G | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-4695T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782177 | ||||||
| chrX:150782204
|
T | TA | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.497-4723dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782204 | ||||||
| chrX:150782257
|
CAAAG | C | 1 | a0001c0001t0002g0087 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.497-4779_497-4776d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782257 | ||||||
| chrX:150782376
|
AG | A | 1 | a0001c0001t0023g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.497-4895delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782376 | ||||||
| chrX:150782557
|
C | T | 2 | a0001c0002t0001g0181a0001c0005t0001g0130 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.497-5075G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782557 | ||||||
| chrX:150782687
|
G | A | 1 | a0001c0001t0010g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.497-5205C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782687 | ||||||
| chrX:150782804
|
T | C | 1 | a0001c0001t0009g0180 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.497-5322A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782804 | ||||||
| chrX:150782825
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-5343A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782825 | ||||||
| chrX:150782879
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0008g0161 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.497-5397T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150782879 | ||||||
| chrX:150783015
|
T | C | 1 | a0001c0001t0005g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.497-5533A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783015 | ||||||
| chrX:150783142
|
CG | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.497-5661delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783142 | ||||||
| chrX:150783150
|
A | AG | 2 | a0001c0001t0001g0062a0001c0001t0010g0177 | 2 | HG02738.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.497-5669dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783150 | ||||||
| chrX:150783240
|
G | A | 2 | a0001c0001t0001g0015a0001c0002t0002g0010 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497-5758C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783240 | ||||||
| chrX:150783261
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0087a0001c0001t0002g0118 | 3 | HG01074.hp1 HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.497-5779G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783261 | ||||||
| chrX:150783285
|
AG | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.497-5804delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783285 | ||||||
| chrX:150783301
|
C | A | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.497-5819G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783301 | ||||||
| chrX:150783309
|
C | A | 27 | a0001c0001t0001g0086a0001c0001t0001g0162a0001c0001t0001g0165others(24): Show | 27 | HG00099.hp1 HG01070.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.497-5827G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783309 | ||||||
| chrX:150783445
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0079 | 2 | NA18966.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.497-5963T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783445 | ||||||
| chrX:150784046
|
G | GC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.497-6565dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784046 | ||||||
| chrX:150784115
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.497-6633C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784115 | ||||||
| chrX:150784118
|
T | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.497-6636A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784118 | ||||||
| chrX:150784154
|
C | T | 45 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.497-6672G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784154 | ||||||
| chrX:150784182
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.497-6700C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784182 | ||||||
| chrX:150784263
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 121 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.497-6781G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784263 | ||||||
| chrX:150784272
|
T | TC | 1 | a0001c0001t0001g0040 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.497-6791dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784272 | ||||||
| chrX:150784425
|
A | G | 3 | a0001c0001t0007g0204a0001c0001t0017g0020a0001c0001t0017g0194 | 3 | HG02280.hp2 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.497-6943T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784425 | ||||||
| chrX:150784465
|
C | T | 14 | a0001c0001t0001g0165a0001c0001t0001g0184a0001c0001t0001g0186others(11): Show | 14 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-6983G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784465 | ||||||
| chrX:150784596
|
T | A | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.497-7114A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784596 | ||||||
| chrX:150785129
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.497-7647T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150785129 | ||||||
| chrX:150785420
|
A | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.497-7938T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150785420 | ||||||
| chrX:150785930
|
A | AC | 1 | a0001c0001t0001g0126 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.496+7760_496+7761i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150785930 | ||||||
| chrX:150786139
|
T | A | 1 | a0001c0002t0002g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.496+7552A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786139 | ||||||
| chrX:150786216
|
G | GT | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.496+7474dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786216 | ||||||
| chrX:150786216
|
GT | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0053 | 2 | HG02056.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.496+7474delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786216 | ||||||
| chrX:150786225
|
T | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.496+7466A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786225 | ||||||
| chrX:150786227
|
T | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0115a0001c0001t0001g0192others(1): Show | 4 | HG01884.hp1 HG02486.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+7464A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786227 | ||||||
| chrX:150786234
|
T | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.496+7457A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786234 | ||||||
| chrX:150786510
|
T | C | 19 | a0001c0001t0001g0115a0001c0001t0001g0175a0001c0001t0001g0183others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.496+7181A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786510 | ||||||
| chrX:150786777
|
T | C | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.496+6914A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786777 | ||||||
| chrX:150786932
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.496+6759A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786932 | ||||||
| chrX:150787006
|
A | G | 5 | a0001c0001t0001g0162a0001c0001t0014g0159a0001c0001t0014g0160others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+6685T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787006 | ||||||
| chrX:150787046
|
G | A | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.496+6645C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787046 | ||||||
| chrX:150787072
|
T | C | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.496+6619A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787072 | ||||||
| chrX:150787743
|
C | T | 2 | a0001c0001t0001g0041a0001c0002t0001g0009 | 2 | HG00438.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.496+5948G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787743 | ||||||
| chrX:150787774
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.496+5917G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787774 | ||||||
| chrX:150787855
|
C | T | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.496+5836G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787855 | ||||||
| chrX:150787888
|
G | GTA | 16 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0090others(13): Show | 16 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.496+5801_496+5802d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
G | GTATA | 10 | a0001c0001t0001g0084a0001c0001t0001g0134a0001c0001t0002g0140others(7): Show | 10 | HG00323.hp2 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+5799_496+5802d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
G | GTATATA | 3 | a0001c0001t0001g0091a0001c0001t0002g0054a0003c0004t0042g0209 | 3 | HG01168.hp2 HG02083.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.496+5797_496+5802d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0112others(4): Show | 7 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+5795_496+5802d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0015g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.496+5793_496+5802d others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
GTA | G | 34 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0034others(31): Show | 34 | HG00438.hp2 HG01081.hp1 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.496+5801_496+5802d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
GTATA | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(54): Show | 58 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.496+5799_496+5802d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
GTATATA | G | 2 | a0001c0001t0001g0077a0001c0001t0017g0020 | 2 | HG00735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.496+5797_496+5802d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
GTATATAT others(1): Show |
G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(4): Show | 7 | HG01070.hp1 HG01109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+5795_496+5802d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
GTATATAT others(3): Show |
G | 18 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0041others(15): Show | 18 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.496+5793_496+5802d others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
GTATATAT others(5): Show |
G | 7 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+5791_496+5802d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
GTATATAT others(11): Show |
G | 1 | a0001c0001t0009g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.496+5785_496+5802d others(20): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787888
|
GTATATAT others(13): Show |
G | 34 | a0001c0001t0001g0115a0001c0001t0001g0165a0001c0001t0001g0175others(31): Show | 34 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.496+5783_496+5802d others(22): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787888 | ||||||
| chrX:150787923
|
TATA | T | 1 | a0001c0001t0020g0060 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.496+5765_496+5767d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150787923 | ||||||
| chrX:150788109
|
T | C | 91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.496+5582A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150788109 | ||||||
| chrX:150788375
|
C | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.496+5316G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150788375 | ||||||
| chrX:150788704
|
C | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.496+4987G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150788704 | ||||||
| chrX:150788779
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 120 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.496+4912T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150788779 | ||||||
| chrX:150788955
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004 | 3 | HG00735.hp1 HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.496+4736T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150788955 | ||||||
| chrX:150789043
|
T | C | 1 | a0001c0001t0036g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+4648A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789043 | ||||||
| chrX:150789124
|
CT | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.496+4566delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789124 | ||||||
| chrX:150789124
|
CTT | C | 7 | a0001c0001t0001g0014a0001c0001t0008g0168a0001c0001t0014g0159others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+4565_496+4566d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789124 | ||||||
| chrX:150789124
|
CTTTTTTT others(1): Show |
C | 1 | a0001c0001t0010g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.496+4559_496+4566d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789124 | ||||||
| chrX:150789192
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.496+4499T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789192 | ||||||
| chrX:150789225
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.496+4466G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789225 | ||||||
| chrX:150789521
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.496+4170A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789521 | ||||||
| chrX:150789547
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.496+4144T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789547 | ||||||
| chrX:150789658
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.496+4033T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789658 | ||||||
| chrX:150789994
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.496+3697A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789994 | ||||||
| chrX:150790100
|
A | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.496+3591T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150790100 | ||||||
| chrX:150790434
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.496+3257T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150790434 | ||||||
| chrX:150790529
|
G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.496+3162C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150790529 | ||||||
| chrX:150790677
|
T | C | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+3014A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150790677 | ||||||
| chrX:150790687
|
G | A | 1 | a0001c0001t0005g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.496+3004C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150790687 | ||||||
| chrX:150790713
|
A | G | 1 | a0001c0001t0034g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.496+2978T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150790713 | ||||||
| chrX:150790821
|
G | T | 15 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+2870C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150790821 | ||||||
| chrX:150791096
|
C | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0157 | 3 | NA18966.hp1 NA19058.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.496+2595G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791096 | ||||||
| chrX:150791108
|
T | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.496+2583A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791108 | ||||||
| chrX:150791292
|
C | T | 1 | a0001c0001t0023g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.496+2399G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791292 | ||||||
| chrX:150791501
|
G | T | 1 | a0001c0001t0009g0180 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.496+2190C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791501 | ||||||
| chrX:150791611
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0206 | 2 | NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.496+2080T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791611 | ||||||
| chrX:150791740
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(22): Show | 25 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.496+1951G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791740 | ||||||
| chrX:150791741
|
G | A | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.496+1950C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791741 | ||||||
| chrX:150791823
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.496+1868T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791823 | ||||||
| chrX:150791917
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.496+1774C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791917 | ||||||
| chrX:150792008
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 120 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.496+1683T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150792008 | ||||||
| chrX:150792134
|
ATCT | A | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.496+1554_496+1556d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150792134 | ||||||
| chrX:150792321
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0205 | 2 | NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.496+1370C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150792321 | ||||||
| chrX:150792427
|
A | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.496+1264T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150792427 | ||||||
| chrX:150792646
|
T | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.496+1045A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150792646 | ||||||
| chrX:150792712
|
C | G | 3 | a0001c0001t0007g0204a0001c0001t0017g0020a0001c0001t0017g0194 | 3 | HG02280.hp2 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.496+979G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150792712 | ||||||
| chrX:150792981
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.496+710T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150792981 | ||||||
| chrX:150793009
|
G | C | 1 | a0001c0001t0023g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.496+682C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150793009 | ||||||
| chrX:150793186
|
C | G | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.496+505G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150793186 | ||||||
| chrX:150793197
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.496+494T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150793197 | ||||||
| chrX:150793311
|
G | A | 1 | a0001c0001t0023g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.496+380C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150793311 | ||||||
| chrX:150793397
|
GTTA | G | 1 | a0001c0001t0001g0108 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.496+291_496+293del others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150793397 | ||||||
| chrX:150793450
|
C | T | 1 | a0001c0001t0004g0088 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.496+241G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150793450 | ||||||
| chrX:150793840
|
GA | G | 1 | a0001c0001t0004g0122 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.431-85delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150793840 | ||||||
| chrX:150793849
|
TCCCAGTT others(13): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.431-113_431-94delC others(19): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150793849 | ||||||
| chrX:150793892
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.431-136A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150793892 | ||||||
| chrX:150793901
|
AC | A | 2 | a0001c0001t0008g0142a0001c0001t0029g0116 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.431-146delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150793901 | ||||||
| chrX:150793928
|
G | A | 2 | a0001c0001t0043g0211a0001c0001t0044g0210 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.431-172C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150793928 | ||||||
| chrX:150793998
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.431-242C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150793998 | ||||||
| chrX:150794081
|
G | C | 1 | a0001c0001t0026g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.431-325C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794081 | ||||||
| chrX:150794128
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-372C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794128 | ||||||
| chrX:150794191
|
T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-435A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794191 | ||||||
| chrX:150794199
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.431-443G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794199 | ||||||
| chrX:150794218
|
G | C | 1 | a0001c0001t0010g0019 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.431-462C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794218 | ||||||
| chrX:150794238
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.431-482C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794238 | ||||||
| chrX:150794257
|
A | G | 1 | a0001c0001t0015g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.431-501T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794257 | ||||||
| chrX:150794456
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.431-700C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794456 | ||||||
| chrX:150794572
|
G | C | 2 | a0001c0001t0002g0081a0001c0001t0006g0046 | 2 | HG01106.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.430+634C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794572 | ||||||
| chrX:150794579
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.430+627C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794579 | ||||||
| chrX:150794580
|
A | G | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198 | 3 | HG02145.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.430+626T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794580 | ||||||
| chrX:150794618
|
C | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.430+588G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794618 | ||||||
| chrX:150794855
|
G | A | 1 | a0001c0001t0023g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.430+351C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794855 | ||||||
| chrX:150794860
|
G | A | 8 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(5): Show | 8 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+346C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794860 | ||||||
| chrX:150794861
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+345G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794861 | ||||||
| chrX:150794923
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.430+283A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794923 | ||||||
| chrX:150794971
|
G | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0184a0001c0001t0001g0186others(13): Show | 16 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.430+235C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150794971 | ||||||
| chrX:150795169
|
T | A | 1 | a0001c0001t0017g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.430+37A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150795169 | ||||||
| chrX:150795334
|
T | C | 1 | a0001c0001t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-45A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 5/10 | chrX | 150795334 | ||||||
| chrX:150795336
|
TG | T | 1 | a0001c0001t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.347-48delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 5/10 | chrX | 150795336 | ||||||
| chrX:150795498
|
A | AG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-13dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150795498 | ||||||
| chrX:150795665
|
G | T | 1 | a0001c0001t0003g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.278-179C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150795665 | ||||||
| chrX:150795682
|
T | C | 18 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0184others(15): Show | 18 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.278-196A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150795682 | ||||||
| chrX:150796156
|
G | A | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.278-670C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796156 | ||||||
| chrX:150796199
|
GA | G | 1 | a0001c0001t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.278-714delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796199 | ||||||
| chrX:150796270
|
T | C | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.278-784A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796270 | ||||||
| chrX:150796285
|
G | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.278-799C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796285 | ||||||
| chrX:150796374
|
C | T | 2 | a0001c0001t0028g0074a0001c0001t0037g0143 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.278-888G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796374 | ||||||
| chrX:150796378
|
AC | A | 1 | a0001c0001t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.278-893delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796378 | ||||||
| chrX:150796429
|
G | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.278-943C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796429 | ||||||
| chrX:150796676
|
GC | G | 1 | a0001c0001t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.278-1191delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796676 | ||||||
| chrX:150796752
|
TA | T | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.278-1267delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796752 | ||||||
| chrX:150796843
|
GA | G | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.278-1358delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796843 | ||||||
| chrX:150796856
|
T | TC | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.278-1371dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796856 | ||||||
| chrX:150796904
|
G | A | 1 | a0001c0001t0004g0122 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.278-1418C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150796904 | ||||||
| chrX:150797072
|
AC | A | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198 | 3 | HG02145.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.278-1587delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797072 | ||||||
| chrX:150797118
|
A | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.278-1632T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797118 | ||||||
| chrX:150797144
|
A | T | 18 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0184others(15): Show | 18 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.278-1658T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797144 | ||||||
| chrX:150797172
|
A | C | 1 | a0001c0001t0004g0052 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.278-1686T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797172 | ||||||
| chrX:150797195
|
T | TA | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.278-1710dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797195 | ||||||
| chrX:150797221
|
T | C | 18 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0184others(15): Show | 18 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.278-1735A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797221 | ||||||
| chrX:150797512
|
C | T | 1 | a0001c0002t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.278-2026G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797512 | ||||||
| chrX:150797578
|
CCT | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2094_278-2093d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797578 | ||||||
| chrX:150797599
|
CA | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2114delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797599 | ||||||
| chrX:150797655
|
TC | T | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2170delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797655 | ||||||
| chrX:150797693
|
C | CA | 1 | a0001c0001t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.278-2208dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797693 | ||||||
| chrX:150797728
|
CA | C | 1 | a0001c0001t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.278-2243delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797728 | ||||||
| chrX:150797732
|
C | G | 1 | a0001c0001t0003g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.278-2246G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797732 | ||||||
| chrX:150797783
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.278-2297C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797783 | ||||||
| chrX:150797869
|
TC | T | 1 | a0001c0001t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.278-2384delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797869 | ||||||
| chrX:150797883
|
A | C | 1 | a0001c0001t0005g0203 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.278-2397T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797883 | ||||||
| chrX:150797886
|
A | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2400T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797886 | ||||||
| chrX:150797913
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278-2427G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797913 | ||||||
| chrX:150797998
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.278-2512G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797998 | ||||||
| chrX:150798028
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.278-2542A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798028 | ||||||
| chrX:150798036
|
C | CA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2551_278-2550i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798036 | ||||||
| chrX:150798039
|
C | CA | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.278-2554dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798039 | ||||||
| chrX:150798039
|
CA | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2554delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798039 | ||||||
| chrX:150798046
|
AAAG | A | 6 | a0001c0001t0001g0184a0001c0001t0002g0140a0001c0001t0008g0139others(3): Show | 6 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-2563_278-2561d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798046 | ||||||
| chrX:150798101
|
AGAACACA others(26): Show |
A | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.278-2648_278-2616d others(35): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798101 | ||||||
| chrX:150798105
|
C | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.278-2619G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798105 | ||||||
| chrX:150798107
|
C | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.278-2621G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798107 | ||||||
| chrX:150798131
|
AAAGGAAG others(30): Show |
A | 13 | a0001c0001t0001g0162a0001c0001t0001g0184a0001c0001t0004g0176others(10): Show | 13 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.278-2682_278-2646d others(39): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798131 | ||||||
| chrX:150798139
|
G | A | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.278-2653C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798139 | ||||||
| chrX:150798140
|
A | G | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.278-2654T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798140 | ||||||
| chrX:150798144
|
A | AAGGG | 22 | a0001c0001t0001g0077a0001c0001t0001g0110a0001c0001t0001g0111others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.278-2662_278-2659d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798144 | ||||||
| chrX:150798144
|
A | AAGGGAGG others(1): Show |
3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.278-2666_278-2659d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798144 | ||||||
| chrX:150798144
|
A | G | 2 | a0001c0001t0028g0074a0001c0001t0037g0143 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.278-2658T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798144 | ||||||
| chrX:150798144
|
AAGGGAGG others(34): Show |
A | 2 | a0001c0001t0001g0115a0001c0001t0001g0186 | 2 | HG01884.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.278-2699_278-2659d others(43): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798144 | ||||||
| chrX:150798149
|
A | AG | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.278-2664dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798149 | ||||||
| chrX:150798162
|
GGAAA | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0087a0001c0001t0002g0118 | 3 | HG01074.hp1 HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.278-2680_278-2677d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798162 | ||||||
| chrX:150798164
|
A | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.278-2678T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798164 | ||||||
| chrX:150798164
|
AAAGG | A | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2682_278-2679d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798164 | ||||||
| chrX:150798166
|
A | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.278-2680T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798166 | ||||||
| chrX:150798168
|
G | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.278-2682C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798168 | ||||||
| chrX:150798170
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0087a0001c0001t0002g0118 | 3 | HG01074.hp1 HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.278-2684T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798170 | ||||||
| chrX:150798172
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0087a0001c0001t0002g0118 | 3 | HG01074.hp1 HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.278-2686C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798172 | ||||||
| chrX:150798177
|
AAGGAAGG others(1): Show |
A | 3 | a0001c0001t0001g0037a0001c0001t0001g0080a0001c0001t0001g0132 | 3 | HG02132.hp1 NA18979.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.278-2699_278-2692d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798177 | ||||||
| chrX:150798181
|
AAGGG | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 99 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.278-2699_278-2696d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798181 | ||||||
| chrX:150798181
|
AAGGGAGG others(1): Show |
A | 1 | a0001c0001t0003g0103 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.278-2703_278-2696d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798181 | ||||||
| chrX:150798185
|
G | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.278-2699C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798185 | ||||||
| chrX:150798185
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2699C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798185 | ||||||
| chrX:150798187
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2701C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798187 | ||||||
| chrX:150798189
|
G | A | 17 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.278-2703C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798189 | ||||||
| chrX:150798203
|
G | GGAAA | 2 | a0001c0001t0003g0156a0001c0001t0040g0006 | 2 | HG04204.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.278-2718_278-2717i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798203 | ||||||
| chrX:150798203
|
GGGAGGAA others(1): Show |
G | 11 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0075others(8): Show | 11 | HG03669.hp1 HG03942.hp1 HG04228.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-2725_278-2718d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798203 | ||||||
| chrX:150798203
|
GGGAGGAA others(5): Show |
G | 1 | a0001c0001t0036g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.278-2729_278-2718d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798203 | ||||||
| chrX:150798203
|
GGGAGGAA others(9): Show |
G | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.278-2733_278-2718d others(18): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798203 | ||||||
| chrX:150798205
|
G | A | 12 | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0123others(9): Show | 12 | HG00735.hp2 HG01243.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.278-2719C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798205 | ||||||
| chrX:150798207
|
G | A | 14 | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0123others(11): Show | 14 | HG00735.hp2 HG01243.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.278-2721C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798207 | ||||||
| chrX:150798207
|
GGAAA | G | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-2725_278-2722d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798207 | ||||||
| chrX:150798209
|
A | G | 15 | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0123others(12): Show | 15 | HG00735.hp2 HG01243.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.278-2723T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798209 | ||||||
| chrX:150798209
|
AAAGG | A | 16 | a0001c0001t0001g0162a0001c0001t0001g0184a0001c0001t0001g0186others(13): Show | 16 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.278-2727_278-2724d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798209 | ||||||
| chrX:150798209
|
AAAGGAAG others(1): Show |
A | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(24): Show | 27 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.278-2731_278-2724d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798209 | ||||||
| chrX:150798209
|
AAAGGAAG others(5): Show |
A | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198 | 3 | HG02145.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.278-2735_278-2724d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798209 | ||||||
| chrX:150798209
|
AAAGGAAG others(17): Show |
A | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.278-2747_278-2724d others(26): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798209 | ||||||
| chrX:150798211
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.278-2725T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798211 | ||||||
| chrX:150798213
|
G | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0075others(9): Show | 12 | HG02109.hp1 HG03669.hp1 HG03942.hp1 others(9): Show |
intron_variant | MODIFIER | c.278-2727C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798213 | ||||||
| chrX:150798215
|
A | G | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-2729T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798215 | ||||||
| chrX:150798217
|
G | A | 1 | a0001c0001t0036g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.278-2731C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798217 | ||||||
| chrX:150798219
|
A | G | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-2733T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798219 | ||||||
| chrX:150798221
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.278-2735C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798221 | ||||||
| chrX:150798223
|
A | G | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-2737T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798223 | ||||||
| chrX:150798225
|
G | A | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-2739C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798225 | ||||||
| chrX:150798226
|
A | AAGGGAGG others(1): Show |
1 | a0001c0001t0033g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.278-2741_278-2740i others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798226 | ||||||
| chrX:150798226
|
A | AAGGGAGG others(13): Show |
1 | a0001c0001t0008g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.278-2741_278-2740i others(22): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798226 | ||||||
| chrX:150798226
|
A | G | 2 | a0001c0001t0003g0156a0001c0001t0040g0006 | 2 | HG04204.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.278-2740T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798226 | ||||||
| chrX:150798230
|
A | AAGGG | 2 | a0001c0001t0005g0141a0001c0001t0035g0167 | 2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.278-2745_278-2744i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798230 | ||||||
| chrX:150798230
|
A | AAGGGAGG others(1): Show |
3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.278-2745_278-2744i others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798230 | ||||||
| chrX:150798230
|
A | G | 13 | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0123others(10): Show | 13 | HG00735.hp2 HG02074.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.278-2744T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798230 | ||||||
| chrX:150798231
|
A | AG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2746dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798231 | ||||||
| chrX:150798234
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.278-2748T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798234 | ||||||
| chrX:150798235
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2749T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798235 | ||||||
| chrX:150798238
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.278-2752T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798238 | ||||||
| chrX:150798239
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2753T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798239 | ||||||
| chrX:150798242
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.278-2756T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798242 | ||||||
| chrX:150798243
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2757T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798243 | ||||||
| chrX:150798246
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.278-2760T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798246 | ||||||
| chrX:150798267
|
A | AG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2782dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798267 | ||||||
| chrX:150798273
|
G | GT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2788_278-2787i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798273 | ||||||
| chrX:150798306
|
G | GA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-2821dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798306 | ||||||
| chrX:150798313
|
G | C | 1 | a0001c0001t0004g0052 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.278-2827C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798313 | ||||||
| chrX:150798377
|
C | A | 1 | a0001c0001t0005g0202 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.278-2891G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798377 | ||||||
| chrX:150798430
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.278-2944C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798430 | ||||||
| chrX:150798589
|
A | AG | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.278-3104dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798589 | ||||||
| chrX:150798629
|
G | GA | 1 | a0001c0001t0003g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.278-3144dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798629 | ||||||
| chrX:150798640
|
GA | G | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-3155delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798640 | ||||||
| chrX:150798688
|
A | AC | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.278-3203dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798688 | ||||||
| chrX:150798871
|
C | CT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-3386dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798871 | ||||||
| chrX:150798910
|
C | T | 18 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.278-3424G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798910 | ||||||
| chrX:150798917
|
AT | A | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.278-3432delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798917 | ||||||
| chrX:150798975
|
TC | T | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-3490delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798975 | ||||||
| chrX:150799050
|
TA | T | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.278-3565delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799050 | ||||||
| chrX:150799135
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.278-3649A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799135 | ||||||
| chrX:150799195
|
CA | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-3710delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799195 | ||||||
| chrX:150799255
|
TG | T | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-3770delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799255 | ||||||
| chrX:150799335
|
C | CA | 2 | a0001c0001t0001g0029a0001c0001t0040g0006 | 2 | NA18967.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.278-3850dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799335 | ||||||
| chrX:150799335
|
C | CAA | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-3851_278-3850d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799335 | ||||||
| chrX:150799335
|
CA | C | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.278-3850delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799335 | ||||||
| chrX:150799346
|
AAAC | A | 1 | a0001c0001t0010g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.278-3863_278-3861d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799346 | ||||||
| chrX:150799436
|
G | GC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-3951dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799436 | ||||||
| chrX:150799474
|
A | ATT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-3989_278-3988i others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799474 | ||||||
| chrX:150799480
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.278-3994G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799480 | ||||||
| chrX:150799488
|
T | TG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4003dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799488 | ||||||
| chrX:150799513
|
C | CA | 3 | a0001c0001t0001g0089a0001c0001t0020g0025a0001c0001t0041g0208 | 3 | HG00438.hp2 NA18953.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.278-4028dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799513 | ||||||
| chrX:150799513
|
CA | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(34): Show | 37 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.278-4028delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799513 | ||||||
| chrX:150799526
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4040T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799526 | ||||||
| chrX:150799528
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4042C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799528 | ||||||
| chrX:150799528
|
G | GA | 2 | a0001c0001t0002g0051a0001c0001t0040g0006 | 2 | NA18974.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.278-4043dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799528 | ||||||
| chrX:150799537
|
CA | C | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.278-4052delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799537 | ||||||
| chrX:150799547
|
GT | G | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.278-4062delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799547 | ||||||
| chrX:150799559
|
G | GC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4074dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799559 | ||||||
| chrX:150799583
|
T | TG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4098_278-4097i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799583 | ||||||
| chrX:150799667
|
G | GC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4182dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799667 | ||||||
| chrX:150799741
|
A | AG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4256dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799741 | ||||||
| chrX:150799742
|
G | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.278-4256C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799742 | ||||||
| chrX:150799778
|
TG | T | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.278-4293delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799778 | ||||||
| chrX:150799822
|
CT | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4337delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799822 | ||||||
| chrX:150799887
|
T | A | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.278-4401A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799887 | ||||||
| chrX:150800044
|
G | C | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.278-4558C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800044 | ||||||
| chrX:150800092
|
G | GA | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.278-4607dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800092 | ||||||
| chrX:150800101
|
A | AC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4616dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800101 | ||||||
| chrX:150800117
|
AC | A | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4632delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800117 | ||||||
| chrX:150800213
|
AG | A | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.278-4728delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800213 | ||||||
| chrX:150800257
|
T | TA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4772dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800257 | ||||||
| chrX:150800281
|
G | GA | 1 | a0001c0001t0003g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.278-4796dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800281 | ||||||
| chrX:150800291
|
T | TG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4806dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800291 | ||||||
| chrX:150800317
|
T | TA | 1 | a0001c0001t0003g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.278-4832dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800317 | ||||||
| chrX:150800483
|
C | CA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4998dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800483 | ||||||
| chrX:150800534
|
T | TG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-5049dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800534 | ||||||
| chrX:150800616
|
A | AG | 2 | a0001c0001t0001g0109a0001c0001t0002g0042 | 2 | HG00741.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.278-5131dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800616 | ||||||
| chrX:150800622
|
TC | T | 1 | a0001c0001t0003g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.278-5137delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800622 | ||||||
| chrX:150800701
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-5215C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800701 | ||||||
| chrX:150800756
|
G | A | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(51): Show | 54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.278-5270C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800756 | ||||||
| chrX:150800801
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.278-5315C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800801 | ||||||
| chrX:150800803
|
T | TG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-5318dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800803 | ||||||
| chrX:150800883
|
A | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(51): Show | 54 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.278-5397T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800883 | ||||||
| chrX:150800887
|
C | CG | 2 | a0001c0001t0001g0084a0001c0001t0001g0109 | 2 | HG03710.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.278-5402dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800887 | ||||||
| chrX:150800923
|
CG | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-5438delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800923 | ||||||
| chrX:150800962
|
C | CG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-5477dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800962 | ||||||
| chrX:150800991
|
AT | A | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-5506delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800991 | ||||||
| chrX:150801026
|
C | T | 1 | a0001c0001t0033g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.278-5540G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801026 | ||||||
| chrX:150801031
|
C | CA | 1 | a0001c0001t0002g0107 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.278-5546dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801031 | ||||||
| chrX:150801041
|
AAC | A | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-5557_278-5556d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801041 | ||||||
| chrX:150801043
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0002g0112 | 2 | HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.278-5557G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801043 | ||||||
| chrX:150801044
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-5558T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801044 | ||||||
| chrX:150801051
|
C | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(11): Show | 14 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.278-5565G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801051 | ||||||
| chrX:150801115
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.278-5629A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801115 | ||||||
| chrX:150801417
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.278-5931C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801417 | ||||||
| chrX:150801459
|
C | A | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.278-5973G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801459 | ||||||
| chrX:150801466
|
T | TGTGAGAA others(13): Show |
1 | a0001c0001t0001g0125 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.278-6000_278-5981d others(22): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801466 | ||||||
| chrX:150801522
|
A | G | 4 | a0001c0001t0011g0163a0001c0001t0011g0164a0001c0001t0011g0171others(1): Show | 4 | HG01884.hp2 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-6036T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801522 | ||||||
| chrX:150801622
|
AG | A | 2 | a0001c0001t0001g0008a0001c0001t0037g0143 | 2 | HG01070.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.278-6137delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801622 | ||||||
| chrX:150801623
|
G | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.278-6137C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801623 | ||||||
| chrX:150801623
|
GA | G | 2 | a0001c0001t0005g0202a0001c0001t0005g0203 | 2 | HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.278-6138delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801623 | ||||||
| chrX:150801676
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.278-6190G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801676 | ||||||
| chrX:150801757
|
G | A | 2 | a0001c0001t0021g0117a0001c0001t0021g0150 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.278-6271C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801757 | ||||||
| chrX:150801859
|
G | GA | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198 | 3 | HG02145.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.278-6374dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801859 | ||||||
| chrX:150801894
|
G | A | 1 | a0001c0001t0007g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.278-6408C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801894 | ||||||
| chrX:150801967
|
G | A | 2 | a0001c0001t0004g0035a0001c0001t0015g0128 | 2 | HG00323.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.278-6481C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801967 | ||||||
| chrX:150801995
|
C | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.278-6509G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801995 | ||||||
| chrX:150802076
|
T | C | 14 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0184others(11): Show | 14 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.278-6590A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802076 | ||||||
| chrX:150802111
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.278-6625T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802111 | ||||||
| chrX:150802176
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278-6690G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802176 | ||||||
| chrX:150802489
|
C | T | 13 | a0001c0001t0001g0162a0001c0001t0001g0184a0001c0001t0001g0186others(10): Show | 13 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.278-7003G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802489 | ||||||
| chrX:150802583
|
A | AT | 31 | a0001c0001t0001g0040a0001c0001t0001g0110a0001c0001t0001g0111others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.278-7098dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802583 | ||||||
| chrX:150802583
|
A | ATT | 2 | a0001c0001t0005g0133a0001c0001t0010g0177 | 2 | HG01255.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.278-7099_278-7098d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802583 | ||||||
| chrX:150802583
|
AT | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.278-7098delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802583 | ||||||
| chrX:150802642
|
C | T | 1 | a0001c0001t0005g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.278-7156G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802642 | ||||||
| chrX:150802683
|
G | A | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-7197C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802683 | ||||||
| chrX:150802800
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.278-7314C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802800 | ||||||
| chrX:150802803
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.278-7317C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802803 | ||||||
| chrX:150802817
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.278-7331C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802817 | ||||||
| chrX:150802880
|
C | CT | 12 | a0001c0001t0001g0029a0001c0001t0001g0061a0001c0001t0001g0175others(9): Show | 12 | HG01256.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.278-7395dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
C | CTT | 7 | a0001c0001t0001g0030a0001c0001t0001g0062a0001c0001t0001g0106others(4): Show | 7 | HG00609.hp1 HG00621.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-7396_278-7395d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CT | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0023others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.278-7395delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CTT | C | 5 | a0001c0001t0004g0035a0001c0001t0008g0161a0001c0001t0015g0128others(2): Show | 5 | HG00323.hp1 HG01167.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-7396_278-7395d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CTTT | C | 2 | a0001c0001t0008g0168a0001c0002t0001g0173 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.278-7397_278-7395d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CTTTTTTT others(2): Show |
C | 2 | a0001c0001t0001g0186a0001c0001t0006g0191 | 2 | HG03471.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.278-7403_278-7395d others(11): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0001g0184a0001c0001t0004g0176a0001c0001t0009g0189others(6): Show | 9 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.278-7404_278-7395d others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0041a0001c0001t0003g0098a0001c0001t0003g0127others(2): Show | 5 | HG02027.hp1 HG02074.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-7406_278-7395d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CTTTTTTT others(6): Show |
C | 11 | a0001c0001t0001g0014a0001c0001t0001g0063a0001c0001t0002g0013others(8): Show | 11 | HG00642.hp1 HG01884.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-7407_278-7395d others(15): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CTTTTTTT others(7): Show |
C | 24 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.278-7408_278-7395d others(16): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150802880
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-7410_278-7395d others(18): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | ||||||
| chrX:150803004
|
T | C | 2 | a0001c0001t0002g0012a0001c0001t0002g0013 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.278-7518A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150803004 | ||||||
| chrX:150803043
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.278-7557C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150803043 | ||||||
| chrX:150803115
|
C | T | 1 | a0001c0002t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.278-7629G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150803115 | ||||||
| chrX:150803232
|
C | A | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.278-7746G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150803232 | ||||||
| chrX:150803256
|
A | G | 1 | a0001c0001t0004g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.278-7770T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150803256 | ||||||
| chrX:150803481
|
G | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0126others(1): Show | 4 | NA18966.hp1 NA19058.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-7995C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150803481 | ||||||
| chrX:150803697
|
G | T | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.278-8211C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150803697 | ||||||
| chrX:150804253
|
G | GA | 1 | a0001c0001t0007g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.278-8768dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150804253 | ||||||
| chrX:150804564
|
C | T | 3 | a0001c0001t0011g0163a0001c0001t0011g0164a0001c0001t0011g0171 | 3 | HG01884.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.278-9078G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150804564 | ||||||
| chrX:150804687
|
C | T | 1 | a0001c0001t0003g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.278-9201G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150804687 | ||||||
| chrX:150804698
|
T | C | 1 | a0001c0001t0007g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.278-9212A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150804698 | ||||||
| chrX:150804911
|
C | T | 29 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.278-9425G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150804911 | ||||||
| chrX:150805053
|
C | A | 15 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.278-9567G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805053 | ||||||
| chrX:150805145
|
G | A | 1 | a0001c0001t0008g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.278-9659C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805145 | ||||||
| chrX:150805173
|
GC | G | 1 | a0001c0001t0008g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.277+9688delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805173 | ||||||
| chrX:150805270
|
C | A | 15 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+9592G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805270 | ||||||
| chrX:150805285
|
T | C | 1 | a0001c0001t0014g0160 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.277+9577A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805285 | ||||||
| chrX:150805320
|
T | TG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+9541dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805320 | ||||||
| chrX:150805492
|
G | GT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+9369dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805492 | ||||||
| chrX:150805618
|
T | C | 5 | a0001c0001t0001g0115a0001c0001t0005g0202a0001c0001t0005g0203others(2): Show | 5 | HG01884.hp1 HG01934.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+9244A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805618 | ||||||
| chrX:150805629
|
T | TG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+9232dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805629 | ||||||
| chrX:150805731
|
A | AT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+9130dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805731 | ||||||
| chrX:150805739
|
G | C | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.277+9123C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805739 | ||||||
| chrX:150805746
|
CG | C | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+9115delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805746 | ||||||
| chrX:150805761
|
G | GT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+9100_277+9101i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805761 | ||||||
| chrX:150805778
|
G | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.277+9084C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805778 | ||||||
| chrX:150805987
|
C | CCA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8874_277+8875i others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805987 | ||||||
| chrX:150805988
|
A | T | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8874T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805988 | ||||||
| chrX:150806136
|
A | AC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8725dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806136 | ||||||
| chrX:150806204
|
A | AT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8657dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806204 | ||||||
| chrX:150806312
|
G | C | 2 | a0001c0001t0004g0064a0001c0001t0004g0199 | 2 | HG01978.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.277+8550C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806312 | ||||||
| chrX:150806537
|
A | AT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8324dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806537 | ||||||
| chrX:150806607
|
A | AAG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8253_277+8254d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806607 | ||||||
| chrX:150806706
|
C | A | 1 | a0001c0001t0001g0055 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.277+8156G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806706 | ||||||
| chrX:150806712
|
G | GA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8149dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806712 | ||||||
| chrX:150806747
|
C | CG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8114dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806747 | ||||||
| chrX:150806773
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.277+8089G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806773 | ||||||
| chrX:150806891
|
C | CA | 1 | a0001c0001t0001g0041 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.277+7970dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806891 | ||||||
| chrX:150807123
|
G | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+7739C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807123 | ||||||
| chrX:150807156
|
C | CT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+7705dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807156 | ||||||
| chrX:150807158
|
C | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 136 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.277+7704G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807158 | ||||||
| chrX:150807302
|
A | AG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+7559dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807302 | ||||||
| chrX:150807381
|
T | TG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+7480dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807381 | ||||||
| chrX:150807386
|
C | CA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+7475dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807386 | ||||||
| chrX:150807395
|
C | CT | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+7466dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807395 | ||||||
| chrX:150807415
|
T | TC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+7446dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807415 | ||||||
| chrX:150807462
|
A | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(28): Show | 31 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.277+7400T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807462 | ||||||
| chrX:150807499
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.277+7363T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807499 | ||||||
| chrX:150807526
|
T | C | 18 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.277+7336A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807526 | ||||||
| chrX:150807581
|
T | TC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+7280dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807581 | ||||||
| chrX:150807612
|
A | AC | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+7249_277+7250i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807612 | ||||||
| chrX:150807743
|
CTG | C | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+7117_277+7118d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807743 | ||||||
| chrX:150808219
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.277+6643A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150808219 | ||||||
| chrX:150808320
|
A | T | 6 | a0001c0001t0001g0041a0001c0001t0001g0063a0001c0001t0003g0098others(3): Show | 6 | HG02027.hp1 HG02074.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+6542T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150808320 | ||||||
| chrX:150808321
|
C | G | 6 | a0001c0001t0001g0041a0001c0001t0001g0063a0001c0001t0003g0098others(3): Show | 6 | HG02027.hp1 HG02074.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+6541G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150808321 | ||||||
| chrX:150808567
|
T | C | 1 | a0001c0001t0007g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.277+6295A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150808567 | ||||||
| chrX:150808696
|
C | T | 15 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(12): Show | 15 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.277+6166G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150808696 | ||||||
| chrX:150808860
|
G | A | 15 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+6002C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150808860 | ||||||
| chrX:150809402
|
A | G | 1 | a0001c0001t0014g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.277+5460T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150809402 | ||||||
| chrX:150809552
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.277+5310T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150809552 | ||||||
| chrX:150810251
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(20): Show | 23 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.277+4611C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150810251 | ||||||
| chrX:150810709
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.277+4153C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150810709 | ||||||
| chrX:150811606
|
A | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.277+3256T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150811606 | ||||||
| chrX:150811962
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01070.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.277+2900T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150811962 | ||||||
| chrX:150812172
|
A | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 115 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.277+2690T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150812172 | ||||||
| chrX:150812977
|
CT | C | 16 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0192others(13): Show | 16 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+1884delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150812977 | ||||||
| chrX:150813220
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+1642G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150813220 | ||||||
| chrX:150813369
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.277+1493A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150813369 | ||||||
| chrX:150813568
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.277+1294A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150813568 | ||||||
| chrX:150813824
|
T | C | 1 | a0001c0002t0002g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.277+1038A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150813824 | ||||||
| chrX:150814225
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.277+637G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150814225 | ||||||
| chrX:150814418
|
A | AC | 2 | a0001c0001t0021g0117a0001c0001t0021g0150 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.277+443dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150814418 | ||||||
| chrX:150814528
|
T | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0153a0001c0001t0001g0205 | 3 | HG02015.hp1 NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.277+334A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150814528 | ||||||
| chrX:150814606
|
TAA | T | 1 | a0001c0001t0005g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.277+254_277+255del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150814606 | ||||||
| chrX:150814652
|
G | A | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.277+210C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150814652 | ||||||
| chrX:150815361
|
C | A | 2 | a0001c0001t0043g0211a0001c0001t0044g0210 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.203-425G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 3/10 | chrX | 150815361 | ||||||
| chrX:150815365
|
T | C | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-429A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 3/10 | chrX | 150815365 | ||||||
| chrX:150815615
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+392G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 3/10 | chrX | 150815615 | ||||||
| chrX:150815639
|
C | T | 1 | a0001c0002t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.202+368G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 3/10 | chrX | 150815639 | ||||||
| chrX:150815971
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01070.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.202+36G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 3/10 | chrX | 150815971 | ||||||
| chrX:150816237
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.131-159A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816237 | ||||||
| chrX:150816400
|
C | T | 1 | a0001c0001t0010g0179 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.131-322G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816400 | ||||||
| chrX:150816428
|
C | A | 1 | a0001c0001t0005g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.131-350G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816428 | ||||||
| chrX:150816651
|
G | A | 1 | a0001c0001t0008g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.131-573C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816651 | ||||||
| chrX:150816688
|
C | CATTACTG others(7): Show |
1 | a0001c0001t0001g0061 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-624_131-611dup others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816688 | ||||||
| chrX:150816786
|
T | G | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-708A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816786 | ||||||
| chrX:150816941
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.131-863C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816941 | ||||||
| chrX:150816964
|
G | A | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.131-886C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816964 | ||||||
| chrX:150816989
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.131-911A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150816989 | ||||||
| chrX:150817053
|
G | A | 1 | a0001c0002t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.131-975C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817053 | ||||||
| chrX:150817059
|
A | AG | 3 | a0001c0001t0001g0154a0001c0001t0001g0186a0001c0001t0004g0199 | 3 | HG01496.hp1 HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.131-982dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817059 | ||||||
| chrX:150817060
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(20): Show | 23 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-982C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817060 | ||||||
| chrX:150817218
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.131-1140A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817218 | ||||||
| chrX:150817226
|
T | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-1148A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817226 | ||||||
| chrX:150817234
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.131-1156A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817234 | ||||||
| chrX:150817243
|
A | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(20): Show | 23 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-1165T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817243 | ||||||
| chrX:150817294
|
T | G | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.131-1216A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817294 | ||||||
| chrX:150817342
|
T | TA | 1 | a0001c0001t0039g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.131-1265dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817342 | ||||||
| chrX:150817351
|
T | A | 1 | a0001c0001t0001g0034 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.131-1273A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817351 | ||||||
| chrX:150817407
|
T | TA | 1 | a0001c0001t0013g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.131-1330dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817407 | ||||||
| chrX:150817532
|
C | CT | 6 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0126others(3): Show | 6 | NA18945.hp1 NA18960.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-1455dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817532 | ||||||
| chrX:150817649
|
G | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-1571C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817649 | ||||||
| chrX:150817743
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.131-1665G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817743 | ||||||
| chrX:150817982
|
G | A | 1 | a0001c0002t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.131-1904C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817982 | ||||||
| chrX:150818019
|
A | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(28): Show | 31 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.131-1941T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818019 | ||||||
| chrX:150818051
|
C | CATAATAA others(19): Show |
20 | a0001c0001t0001g0037a0001c0001t0001g0110a0001c0001t0001g0111others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.131-1974_131-1973i others(28): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818051 | ||||||
| chrX:150818053
|
T | TAATAATT others(17): Show |
5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-1976_131-1975i others(26): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818053 | ||||||
| chrX:150818053
|
T | TAATAATT others(18): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0077 | 2 | HG00735.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.131-1976_131-1975i others(27): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818053 | ||||||
| chrX:150818053
|
T | TAATAATT others(19): Show |
22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(19): Show | 22 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.131-1976_131-1975i others(28): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818053 | ||||||
| chrX:150818201
|
G | GAT | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 120 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.131-2125_131-2124d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATAT | 5 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0001g0187others(2): Show | 5 | HG00140.hp1 HG01070.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2127_131-2124d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(7): Show |
2 | a0001c0001t0009g0195a0001c0001t0017g0020 | 2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.131-2137_131-2124d others(16): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(9): Show |
5 | a0001c0001t0001g0077a0001c0001t0007g0196a0001c0001t0007g0197others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2139_131-2124d others(18): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(11): Show |
7 | a0001c0001t0001g0111a0001c0001t0001g0134a0001c0001t0002g0039others(4): Show | 7 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-2141_131-2124d others(20): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(13): Show |
5 | a0001c0001t0002g0042a0001c0001t0002g0137a0001c0001t0002g0138others(2): Show | 5 | HG00741.hp2 HG01168.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2143_131-2124d others(22): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(15): Show |
2 | a0001c0001t0006g0044a0001c0002t0002g0010 | 2 | HG01081.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.131-2145_131-2124d others(24): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(17): Show |
4 | a0001c0001t0001g0037a0001c0001t0001g0110a0001c0001t0009g0180others(1): Show | 4 | HG00099.hp2 NA18979.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-2124_131-2123i others(26): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(19): Show |
7 | a0001c0001t0001g0014a0001c0001t0002g0012a0001c0001t0008g0142others(4): Show | 7 | HG01192.hp1 HG01496.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-2124_131-2123i others(28): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(21): Show |
3 | a0001c0001t0002g0016a0001c0001t0028g0074a0001c0001t0036g0145 | 3 | HG02630.hp1 HG03209.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.131-2124_131-2123i others(30): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(23): Show |
5 | a0001c0001t0001g0008a0001c0001t0002g0013a0001c0001t0002g0017others(2): Show | 5 | HG00408.hp1 HG00642.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2124_131-2123i others(32): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(25): Show |
3 | a0001c0001t0011g0171a0001c0001t0013g0078a0001c0001t0025g0144 | 3 | HG02886.hp1 HG04115.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.131-2124_131-2123i others(34): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(27): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0018others(2): Show | 5 | HG00438.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2124_131-2123i others(36): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818201
|
G | GATATATA others(31): Show |
1 | a0001c0001t0039g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.131-2124_131-2123i others(40): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818201 | ||||||
| chrX:150818217
|
T | C | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-2139A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818217 | ||||||
| chrX:150818310
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.131-2232A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818310 | ||||||
| chrX:150818528
|
C | CAA | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.131-2452_131-2451d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818528 | ||||||
| chrX:150818709
|
A | T | 6 | a0001c0001t0001g0077a0001c0001t0007g0196a0001c0001t0007g0197others(3): Show | 6 | HG00735.hp2 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-2631T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818709 | ||||||
| chrX:150818795
|
G | C | 3 | a0001c0001t0001g0157a0001c0001t0018g0104a0001c0001t0018g0105 | 3 | NA18945.hp1 NA18960.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.131-2717C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150818795 | ||||||
| chrX:150819050
|
C | T | 4 | a0001c0001t0001g0115a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-2972G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150819050 | ||||||
| chrX:150819528
|
C | G | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-3450G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150819528 | ||||||
| chrX:150819790
|
TA | T | 1 | a0001c0001t0001g0097 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.131-3713delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150819790 | ||||||
| chrX:150820055
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.131-3977A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150820055 | ||||||
| chrX:150820264
|
GA | G | 37 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.131-4187delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150820264 | ||||||
| chrX:150820264
|
GAA | G | 1 | a0001c0001t0001g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.131-4188_131-4187d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150820264 | ||||||
| chrX:150820406
|
C | T | 4 | a0001c0001t0004g0035a0001c0001t0004g0064a0001c0001t0004g0199others(1): Show | 4 | HG00323.hp1 HG01167.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-4328G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150820406 | ||||||
| chrX:150820806
|
A | G | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-4728T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150820806 | ||||||
| chrX:150821047
|
G | A | 1 | a0001c0002t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.131-4969C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150821047 | ||||||
| chrX:150821173
|
T | C | 6 | a0001c0001t0001g0077a0001c0001t0007g0196a0001c0001t0007g0197others(3): Show | 6 | HG00735.hp2 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-5095A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150821173 | ||||||
| chrX:150821227
|
G | T | 1 | a0001c0001t0009g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.131-5149C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150821227 | ||||||
| chrX:150821456
|
C | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.131-5378G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150821456 | ||||||
| chrX:150821463
|
T | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.131-5385A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150821463 | ||||||
| chrX:150821583
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.131-5505G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150821583 | ||||||
| chrX:150821756
|
G | A | 1 | a0001c0001t0017g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.131-5678C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150821756 | ||||||
| chrX:150822277
|
A | G | 1 | a0001c0001t0011g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.131-6199T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150822277 | ||||||
| chrX:150822301
|
T | C | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-6223A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150822301 | ||||||
| chrX:150822402
|
A | AT | 2 | a0001c0001t0001g0056a0001c0001t0001g0101 | 2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.131-6325dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150822402 | ||||||
| chrX:150822746
|
A | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.131-6668T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150822746 | ||||||
| chrX:150822772
|
TA | T | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-6695delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150822772 | ||||||
| chrX:150822907
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.131-6829C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150822907 | ||||||
| chrX:150822967
|
G | A | 5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-6889C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150822967 | ||||||
| chrX:150823037
|
ACTT | A | 1 | a0001c0001t0025g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.131-6962_131-6960d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823037 | ||||||
| chrX:150823126
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.131-7048T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823126 | ||||||
| chrX:150823308
|
C | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-7230G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823308 | ||||||
| chrX:150823371
|
T | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.131-7293A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823371 | ||||||
| chrX:150823442
|
C | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-7364G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823442 | ||||||
| chrX:150823502
|
T | TC | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.131-7425dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823502 | ||||||
| chrX:150823746
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004 | 3 | HG00735.hp1 HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.130+7485C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823746 | ||||||
| chrX:150823795
|
T | TC | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+7435dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823795 | ||||||
| chrX:150823804
|
CATG | C | 2 | a0001c0001t0016g0072a0001c0001t0016g0073 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.130+7424_130+7426d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823804 | ||||||
| chrX:150823868
|
G | GA | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+7362dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823868 | ||||||
| chrX:150823987
|
AAAG | A | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198 | 3 | HG02145.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.130+7241_130+7243d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150823987 | ||||||
| chrX:150824004
|
A | AGAG | 1 | a0001c0001t0001g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130+7224_130+7226d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824004 | ||||||
| chrX:150824007
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0002g0039a0001c0001t0002g0042others(3): Show | 6 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+7224C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824007 | ||||||
| chrX:150824025
|
A | AGAG | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+7203_130+7205d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824025 | ||||||
| chrX:150824025
|
AGAG | A | 2 | a0001c0001t0001g0193a0001c0001t0043g0211 | 2 | HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.130+7203_130+7205d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824025 | ||||||
| chrX:150824025
|
AGAGGAG | A | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.130+7200_130+7205d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824025 | ||||||
| chrX:150824046
|
A | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+7185T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824046 | ||||||
| chrX:150824055
|
G | A | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+7176C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824055 | ||||||
| chrX:150824058
|
GGAGGAA | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+7167_130+7172d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824058 | ||||||
| chrX:150824062
|
GA | G | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+7168delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824062 | ||||||
| chrX:150824080
|
GAAGAAGA others(3): Show |
G | 1 | a0001c0001t0004g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.130+7141_130+7150d others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824080 | ||||||
| chrX:150824092
|
A | AGAAGAAG | 1 | a0001c0001t0003g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130+7132_130+7138d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824092 | ||||||
| chrX:150824092
|
AGAAGAAG | A | 12 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0094others(9): Show | 12 | HG00323.hp1 HG00408.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+7132_130+7138d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824092 | ||||||
| chrX:150824099
|
G | A | 1 | a0001c0001t0004g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.130+7132C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824099 | ||||||
| chrX:150824115
|
AAGAAGGA others(6): Show |
A | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.130+7103_130+7115d others(15): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824115 | ||||||
| chrX:150824122
|
AAGG | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+7106_130+7108d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824122 | ||||||
| chrX:150824143
|
A | G | 2 | a0001c0001t0002g0140a0001c0001t0008g0139 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.130+7088T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824143 | ||||||
| chrX:150824150
|
A | AAGG | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130+7078_130+7080d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824150 | ||||||
| chrX:150824150
|
AAGG | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.130+7078_130+7080d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824150 | ||||||
| chrX:150824150
|
AAGGAGG | A | 5 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(2): Show | 5 | HG02451.hp1 NA18522.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+7075_130+7080d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824150 | ||||||
| chrX:150824154
|
A | C | 1 | a0001c0001t0001g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.130+7077T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824154 | ||||||
| chrX:150824162
|
GAGGAGGA others(8): Show |
G | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+7054_130+7068d others(17): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824162 | ||||||
| chrX:150824170
|
GGAGGAGA others(20): Show |
G | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+7034_130+7060d others(29): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824170 | ||||||
| chrX:150824171
|
G | GAGA | 23 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0184others(20): Show | 23 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.130+7059_130+7060i others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824171 | ||||||
| chrX:150824171
|
G | GAGGAGGA others(2): Show |
2 | a0001c0001t0005g0141a0001c0001t0035g0167 | 2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.130+7059_130+7060i others(11): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824171 | ||||||
| chrX:150824171
|
G | GAGGAGGA others(5): Show |
3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+7059_130+7060i others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824171 | ||||||
| chrX:150824173
|
GGAGAAGG others(11): Show |
G | 1 | a0001c0001t0001g0029 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.130+7040_130+7057d others(20): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824173 | ||||||
| chrX:150824174
|
G | GAGGAGA | 1 | a0001c0001t0001g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.130+7056_130+7057i others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824174 | ||||||
| chrX:150824177
|
A | AAGG | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 108 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.130+7051_130+7053d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824177 | ||||||
| chrX:150824177
|
A | AAGGAGG | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.130+7048_130+7053d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824177 | ||||||
| chrX:150824177
|
A | G | 29 | a0001c0001t0001g0123a0001c0001t0001g0175a0001c0001t0001g0183others(26): Show | 29 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.130+7054T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824177 | ||||||
| chrX:150824183
|
G | GAGGAGA | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130+7047_130+7048i others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824183 | ||||||
| chrX:150824187
|
A | AGGAG | 1 | a0001c0001t0001g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130+7043_130+7044i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824187 | ||||||
| chrX:150824191
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(109): Show | 113 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.130+7040T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824191 | ||||||
| chrX:150824194
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0107 | 3 | HG01258.hp1 HG01261.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.130+7037T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824194 | ||||||
| chrX:150824200
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0107 | 3 | HG01258.hp1 HG01261.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.130+7031C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824200 | ||||||
| chrX:150824203
|
G | A | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+7028C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824203 | ||||||
| chrX:150824206
|
G | A | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+7025C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824206 | ||||||
| chrX:150824235
|
AAAG | A | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.130+6993_130+6995d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824235 | ||||||
| chrX:150824239
|
AAGAAGG | A | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130+6986_130+6991d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824239 | ||||||
| chrX:150824242
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.130+6989T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824242 | ||||||
| chrX:150824242
|
AAGG | A | 12 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(9): Show | 12 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+6986_130+6988d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824242 | ||||||
| chrX:150824246
|
A | AG | 1 | a0001c0001t0001g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130+6984dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824246 | ||||||
| chrX:150824265
|
A | AAGG | 8 | a0001c0001t0001g0115a0001c0001t0005g0202a0001c0001t0005g0203others(5): Show | 8 | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+6963_130+6965d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824265 | ||||||
| chrX:150824265
|
AAGG | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0110others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.130+6963_130+6965d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824265 | ||||||
| chrX:150824283
|
G | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(35): Show | 38 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.130+6948C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824283 | ||||||
| chrX:150824284
|
A | AAG | 24 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.130+6946_130+6947i others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824284 | ||||||
| chrX:150824285
|
G | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(11): Show | 14 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+6946C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824285 | ||||||
| chrX:150824286
|
A | G | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(11): Show | 14 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+6945T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824286 | ||||||
| chrX:150824287
|
A | AG | 24 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.130+6943_130+6944i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824287 | ||||||
| chrX:150824287
|
A | G | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(11): Show | 14 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+6944T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824287 | ||||||
| chrX:150824289
|
G | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(35): Show | 38 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.130+6942C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824289 | ||||||
| chrX:150824304
|
A | AGAAGAGG others(2): Show |
1 | a0001c0001t0007g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.130+6926_130+6927i others(11): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824304 | ||||||
| chrX:150824304
|
A | G | 24 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.130+6927T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824304 | ||||||
| chrX:150824304
|
AGAG | A | 19 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0111others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.130+6924_130+6926d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824304 | ||||||
| chrX:150824307
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0115a0001c0001t0001g0162others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+6924C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824307 | ||||||
| chrX:150824310
|
G | A | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.130+6921C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824310 | ||||||
| chrX:150824323
|
GAGGAGA | G | 1 | a0001c0001t0038g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.130+6902_130+6907d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824323 | ||||||
| chrX:150824329
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130+6902T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824329 | ||||||
| chrX:150824332
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130+6899T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824332 | ||||||
| chrX:150824340
|
GA | G | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130+6890delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824340 | ||||||
| chrX:150824341
|
A | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6890T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824341 | ||||||
| chrX:150824341
|
AAAGAAGG | A | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130+6883_130+6889d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824341 | ||||||
| chrX:150824348
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130+6883C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824348 | ||||||
| chrX:150824361
|
G | GGAAGAA | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6864_130+6869d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824361 | ||||||
| chrX:150824361
|
GGAA | G | 1 | a0001c0001t0001g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130+6867_130+6869d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824361 | ||||||
| chrX:150824372
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.130+6859T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824372 | ||||||
| chrX:150824375
|
AAGAAGAA others(2): Show |
A | 12 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(9): Show | 12 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+6847_130+6855d others(11): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824375 | ||||||
| chrX:150824381
|
A | AAAG | 5 | a0001c0001t0001g0115a0001c0001t0004g0035a0001c0001t0005g0202others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+6847_130+6849d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824381 | ||||||
| chrX:150824381
|
AAAG | A | 21 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.130+6847_130+6849d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824381 | ||||||
| chrX:150824381
|
AAAGAAG | A | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.130+6844_130+6849d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824381 | ||||||
| chrX:150824410
|
AAAAGAAG others(3): Show |
A | 1 | a0001c0001t0001g0063 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.130+6811_130+6820d others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824410 | ||||||
| chrX:150824422
|
A | AG | 1 | a0001c0001t0001g0023 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.130+6808_130+6809i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824422 | ||||||
| chrX:150824422
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.130+6809T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824422 | ||||||
| chrX:150824425
|
G | GAGA | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6803_130+6805d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824425 | ||||||
| chrX:150824425
|
G | GAGAAGA | 1 | a0001c0002t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130+6800_130+6805d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824425 | ||||||
| chrX:150824425
|
G | GAGAAGAA others(13): Show |
1 | a0001c0001t0001g0108 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.130+6786_130+6805d others(22): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824425 | ||||||
| chrX:150824425
|
GAGAAGAA others(13): Show |
G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130+6786_130+6805d others(22): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824425 | ||||||
| chrX:150824430
|
GAAGAAGA | G | 1 | a0001c0001t0004g0122 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.130+6794_130+6800d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824430 | ||||||
| chrX:150824437
|
A | AAAGAAGA others(6): Show |
4 | a0001c0001t0001g0065a0001c0001t0001g0126a0001c0001t0001g0153others(1): Show | 4 | HG02015.hp1 NA19067.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6781_130+6793d others(15): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824437 | ||||||
| chrX:150824437
|
A | AAGAAG | 1 | a0001c0001t0001g0063 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.130+6793_130+6794i others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824437 | ||||||
| chrX:150824437
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.130+6794T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824437 | ||||||
| chrX:150824443
|
G | GAAGA | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.130+6787_130+6788i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824443 | ||||||
| chrX:150824443
|
GA | G | 1 | a0001c0002t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130+6787delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824443 | ||||||
| chrX:150824444
|
A | AAG | 3 | a0001c0001t0001g0023a0001c0001t0001g0062a0001c0001t0020g0060 | 3 | NA18943.hp1 NA18979.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.130+6786_130+6787i others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824444 | ||||||
| chrX:150824444
|
AAAG | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.130+6784_130+6786d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824444 | ||||||
| chrX:150824453
|
GAAGA | G | 1 | a0001c0001t0008g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.130+6774_130+6777d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824453 | ||||||
| chrX:150824458
|
A | AG | 1 | a0001c0001t0001g0062 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.130+6772_130+6773i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824458 | ||||||
| chrX:150824464
|
A | AAAG | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6764_130+6766d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824464 | ||||||
| chrX:150824464
|
A | AAAGAAG | 1 | a0001c0001t0001g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.130+6761_130+6766d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824464 | ||||||
| chrX:150824464
|
A | AG | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.130+6766_130+6767i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824464 | ||||||
| chrX:150824473
|
G | GAAGA | 1 | a0001c0001t0002g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.130+6754_130+6757d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824473 | ||||||
| chrX:150824477
|
A | AAG | 1 | a0001c0001t0001g0121 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.130+6753_130+6754i others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824477 | ||||||
| chrX:150824481
|
A | AAG | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.130+6748_130+6749d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824481 | ||||||
| chrX:150824487
|
GAAGAAGA others(3): Show |
G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6734_130+6743d others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824487 | ||||||
| chrX:150824490
|
G | GA | 1 | a0001c0001t0001g0023 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.130+6740dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824490 | ||||||
| chrX:150824497
|
A | AAAG | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.130+6731_130+6733d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824497 | ||||||
| chrX:150824497
|
A | AAG | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.130+6733_130+6734i others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824497 | ||||||
| chrX:150824498
|
A | T | 1 | a0001c0001t0001g0023 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.130+6733T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824498 | ||||||
| chrX:150824503
|
G | GA | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6727dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824503 | ||||||
| chrX:150824508
|
AGAAG | A | 1 | a0001c0001t0023g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.130+6719_130+6722d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824508 | ||||||
| chrX:150824512
|
G | GAA | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6718_130+6719i others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824512 | ||||||
| chrX:150824512
|
G | GAAGAA | 1 | a0001c0001t0013g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130+6718_130+6719i others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824512 | ||||||
| chrX:150824516
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6715C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824516 | ||||||
| chrX:150824523
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6708C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824523 | ||||||
| chrX:150824524
|
A | G | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6707T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824524 | ||||||
| chrX:150824525
|
A | AG | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.130+6705_130+6706i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824525 | ||||||
| chrX:150824534
|
A | G | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6697T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824534 | ||||||
| chrX:150824534
|
AAAGAAGG | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0155a0001c0001t0041g0208 | 3 | HG00438.hp2 HG02040.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.130+6690_130+6696d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824534 | ||||||
| chrX:150824540
|
G | GAAGAA | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6690_130+6691i others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824540 | ||||||
| chrX:150824547
|
GGAA | G | 2 | a0001c0001t0002g0017a0001c0001t0007g0204 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+6681_130+6683d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824547 | ||||||
| chrX:150824550
|
A | AG | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6680dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824550 | ||||||
| chrX:150824562
|
A | AAGG | 22 | a0001c0001t0001g0077a0001c0001t0001g0110a0001c0001t0001g0111others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+6666_130+6668d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824562 | ||||||
| chrX:150824562
|
AAGG | A | 12 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(9): Show | 12 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+6666_130+6668d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824562 | ||||||
| chrX:150824565
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6666C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824565 | ||||||
| chrX:150824568
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6663C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824568 | ||||||
| chrX:150824569
|
AGG | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6660_130+6661d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824569 | ||||||
| chrX:150824571
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6660C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824571 | ||||||
| chrX:150824574
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6657C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824574 | ||||||
| chrX:150824578
|
AGG | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6651_130+6652d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824578 | ||||||
| chrX:150824580
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6651C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824580 | ||||||
| chrX:150824580
|
GAGAAGGA others(5): Show |
G | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130+6639_130+6650d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824580 | ||||||
| chrX:150824586
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6645C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824586 | ||||||
| chrX:150824587
|
AGG | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6642_130+6643d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824587 | ||||||
| chrX:150824592
|
A | G | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6639T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824592 | ||||||
| chrX:150824595
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.130+6636T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824595 | ||||||
| chrX:150824600
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6631C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824600 | ||||||
| chrX:150824602
|
AG | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6628delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824602 | ||||||
| chrX:150824603
|
G | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+6628C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824603 | ||||||
| chrX:150824604
|
GAGA | G | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+6624_130+6626d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824604 | ||||||
| chrX:150824606
|
GA | G | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6624delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824606 | ||||||
| chrX:150824643
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.130+6588T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824643 | ||||||
| chrX:150824644
|
A | AGAAGAAG others(11): Show |
22 | a0001c0001t0001g0077a0001c0001t0001g0110a0001c0001t0001g0111others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+6586_130+6587i others(20): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824644 | ||||||
| chrX:150824647
|
A | AGAAGAAG others(8): Show |
26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.130+6583_130+6584i others(17): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824647 | ||||||
| chrX:150824647
|
A | AGGAGGAG others(20): Show |
1 | a0001c0001t0007g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.130+6583_130+6584i others(29): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824647 | ||||||
| chrX:150824657
|
GAAGA | G | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6570_130+6573d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824657 | ||||||
| chrX:150824662
|
A | AGAG | 7 | a0001c0001t0001g0053a0001c0001t0004g0047a0001c0001t0008g0161others(4): Show | 7 | HG02056.hp1 HG02129.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+6568_130+6569i others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824662 | ||||||
| chrX:150824662
|
A | G | 5 | a0001c0001t0002g0067a0001c0001t0002g0140a0001c0001t0008g0139others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+6569T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824662 | ||||||
| chrX:150824673
|
AG | A | 1 | a0001c0001t0024g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.130+6557delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824673 | ||||||
| chrX:150824674
|
G | A | 12 | a0001c0001t0001g0053a0001c0001t0002g0067a0001c0001t0002g0140others(9): Show | 12 | HG02056.hp1 HG02129.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+6557C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824674 | ||||||
| chrX:150824682
|
A | AAG | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6547_130+6548d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824682 | ||||||
| chrX:150824683
|
A | AGAGGAG | 1 | a0001c0001t0008g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.130+6547_130+6548i others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824683 | ||||||
| chrX:150824683
|
A | G | 12 | a0001c0001t0001g0053a0001c0001t0002g0067a0001c0001t0002g0140others(9): Show | 12 | HG02056.hp1 HG02129.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+6548T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824683 | ||||||
| chrX:150824686
|
A | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+6545T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824686 | ||||||
| chrX:150824704
|
AGAG | A | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.130+6524_130+6526d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824704 | ||||||
| chrX:150824705
|
G | GAAGA | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6525_130+6526i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824705 | ||||||
| chrX:150824707
|
G | A | 15 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0002g0067others(12): Show | 15 | HG02056.hp1 HG02083.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+6524C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824707 | ||||||
| chrX:150824707
|
G | GGAA | 30 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+6521_130+6523d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824707 | ||||||
| chrX:150824707
|
G | GGAAGAA | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 124 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.130+6518_130+6523d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824707 | ||||||
| chrX:150824707
|
G | GGAAGAAG others(2): Show |
5 | a0001c0001t0002g0076a0001c0001t0017g0020a0001c0001t0019g0178others(2): Show | 5 | HG00673.hp1 HG01243.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+6515_130+6523d others(11): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824707 | ||||||
| chrX:150824707
|
G | GGAAGAGG others(14): Show |
7 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(4): Show | 7 | HG01099.hp1 HG02738.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+6523_130+6524i others(23): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824707 | ||||||
| chrX:150824707
|
G | GGAAGAGG others(17): Show |
4 | a0001c0001t0009g0189a0001c0001t0010g0019a0001c0001t0010g0185others(1): Show | 4 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+6523_130+6524i others(26): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824707 | ||||||
| chrX:150824760
|
G | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+6471C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824760 | ||||||
| chrX:150825377
|
C | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.130+5854G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825377 | ||||||
| chrX:150825428
|
T | TC | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+5802dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825428 | ||||||
| chrX:150825521
|
T | TC | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+5709dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825521 | ||||||
| chrX:150825549
|
G | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.130+5682C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825549 | ||||||
| chrX:150825689
|
T | C | 1 | a0001c0001t0003g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.130+5542A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825689 | ||||||
| chrX:150825695
|
A | AG | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+5535dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825695 | ||||||
| chrX:150825792
|
A | AAAAATT | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+5433_130+5438d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825792 | ||||||
| chrX:150825904
|
A | C | 1 | a0001c0002t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.130+5327T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825904 | ||||||
| chrX:150826213
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.130+5018A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150826213 | ||||||
| chrX:150826393
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.130+4838G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150826393 | ||||||
| chrX:150826760
|
C | G | 1 | a0001c0005t0001g0130 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+4471G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150826760 | ||||||
| chrX:150826798
|
G | A | 1 | a0001c0001t0039g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.130+4433C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150826798 | ||||||
| chrX:150827177
|
G | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+4054C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150827177 | ||||||
| chrX:150827545
|
T | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.130+3686A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150827545 | ||||||
| chrX:150828052
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.130+3179T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150828052 | ||||||
| chrX:150828086
|
T | G | 2 | a0001c0001t0001g0187a0001c0001t0006g0082 | 2 | HG00140.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.130+3145A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150828086 | ||||||
| chrX:150828105
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.130+3126G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150828105 | ||||||
| chrX:150828343
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | NA18984.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.130+2888G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150828343 | ||||||
| chrX:150828690
|
A | G | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.130+2541T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150828690 | ||||||
| chrX:150828745
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130+2486C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150828745 | ||||||
| chrX:150828753
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.130+2478C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150828753 | ||||||
| chrX:150828779
|
A | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.130+2452T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150828779 | ||||||
| chrX:150829064
|
G | A | 1 | a0001c0001t0038g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.130+2167C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829064 | ||||||
| chrX:150829189
|
C | T | 19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(16): Show | 19 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+2042G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829189 | ||||||
| chrX:150829264
|
A | C | 1 | a0001c0001t0041g0208 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.130+1967T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829264 | ||||||
| chrX:150829689
|
AAC | A | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.130+1540_130+1541d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829689 | ||||||
| chrX:150829692
|
A | C | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.130+1539T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829692 | ||||||
| chrX:150829876
|
GC | G | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.130+1354delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829876 | ||||||
| chrX:150829909
|
C | A | 1 | a0001c0001t0001g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.130+1322G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829909 | ||||||
| chrX:150830049
|
G | C | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.130+1182C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830049 | ||||||
| chrX:150830308
|
TG | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.130+922delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830308 | ||||||
| chrX:150830370
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(19): Show | 22 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.130+861C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830370 | ||||||
| chrX:150830444
|
T | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.130+787A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830444 | ||||||
| chrX:150830559
|
GA | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.130+671delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830559 | ||||||
| chrX:150830651
|
A | G | 1 | a0001c0001t0005g0203 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+580T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830651 | ||||||
| chrX:150830670
|
T | C | 1 | a0001c0001t0006g0046 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.130+561A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830670 | ||||||
| chrX:150830713
|
C | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.130+518G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830713 | ||||||
| chrX:150830810
|
T | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.130+421A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830810 | ||||||
| chrX:150830830
|
C | T | 15 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(12): Show | 15 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+401G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830830 | ||||||
| chrX:150830898
|
C | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.130+333G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830898 | ||||||
| chrX:150830959
|
A | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.130+272T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830959 | ||||||
| chrX:150830960
|
T | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.130+271A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830960 | ||||||
| chrX:150831209
|
GT | G | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.130+21delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150831209 | ||||||
| chrX:150831223
|
C | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.130+8G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150831223 | ||||||
| chrX:150831302
|
T | TA | 1 | a0001c0001t0013g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.68-10dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831302 | ||||||
| chrX:150831302
|
TA | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0061others(1): Show | 4 | HG01256.hp1 HG02723.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-10delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831302 | ||||||
| chrX:150831689
|
AC | A | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-397delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831689 | ||||||
| chrX:150831712
|
T | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.68-419A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831712 | ||||||
| chrX:150831755
|
T | TA | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-463dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831755 | ||||||
| chrX:150831817
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-524T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831817 | ||||||
| chrX:150831893
|
A | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-600T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831893 | ||||||
| chrX:150831973
|
T | C | 1 | a0001c0001t0016g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68-680A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831973 | ||||||
| chrX:150832141
|
A | G | 2 | a0001c0001t0009g0195a0001c0001t0017g0194 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.68-848T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150832141 | ||||||
| chrX:150832361
|
G | GT | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-1069dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150832361 | ||||||
| chrX:150832461
|
C | CA | 1 | a0001c0001t0020g0060 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.68-1169dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150832461 | ||||||
| chrX:150832846
|
G | C | 1 | a0001c0001t0009g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.68-1553C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150832846 | ||||||
| chrX:150832885
|
TA | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-1593delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150832885 | ||||||
| chrX:150833054
|
C | CA | 4 | a0001c0001t0001g0061a0001c0001t0001g0089a0001c0001t0001g0165others(1): Show | 4 | HG01256.hp1 HG01516.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1762dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833054 | ||||||
| chrX:150833054
|
CA | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(27): Show | 30 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-1762delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833054 | ||||||
| chrX:150833265
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-1972C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833265 | ||||||
| chrX:150833322
|
A | T | 1 | a0001c0001t0033g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-2029T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833322 | ||||||
| chrX:150833644
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-2351A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833644 | ||||||
| chrX:150833663
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-2370A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833663 | ||||||
| chrX:150833839
|
AG | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-2547delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833839 | ||||||
| chrX:150833901
|
AG | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-2609delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833901 | ||||||
| chrX:150833950
|
T | G | 14 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-2657A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833950 | ||||||
| chrX:150833967
|
A | AAAC | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.68-2677_68-2675dup others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833967 | ||||||
| chrX:150834092
|
T | A | 17 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-2799A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834092 | ||||||
| chrX:150834100
|
G | A | 1 | a0001c0005t0001g0130 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.68-2807C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834100 | ||||||
| chrX:150834139
|
T | G | 2 | a0001c0001t0001g0183a0001c0001t0032g0182 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.68-2846A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834139 | ||||||
| chrX:150834171
|
T | G | 1 | a0001c0001t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-2878A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834171 | ||||||
| chrX:150834251
|
T | C | 1 | a0001c0001t0013g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.68-2958A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834251 | ||||||
| chrX:150834354
|
C | CT | 1 | a0001c0001t0033g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68-3062_68-3061ins others(1): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834354 | ||||||
| chrX:150834454
|
T | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.68-3161A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834454 | ||||||
| chrX:150834635
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.68-3342A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834635 | ||||||
| chrX:150834683
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.68-3390T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834683 | ||||||
| chrX:150835030
|
TA | T | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-3738delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150835030 | ||||||
| chrX:150835155
|
A | C | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-3862T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150835155 | ||||||
| chrX:150835188
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0155a0001c0001t0041g0208 | 3 | HG00438.hp2 HG02040.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.68-3895G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150835188 | ||||||
| chrX:150835387
|
C | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(19): Show | 22 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.68-4094G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150835387 | ||||||
| chrX:150835399
|
G | A | 1 | a0001c0001t0044g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.68-4106C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150835399 | ||||||
| chrX:150835943
|
A | G | 4 | a0001c0001t0001g0115a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-4650T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150835943 | ||||||
| chrX:150836002
|
T | C | 17 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-4709A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836002 | ||||||
| chrX:150836008
|
A | G | 19 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0192others(16): Show | 19 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-4715T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836008 | ||||||
| chrX:150836099
|
T | C | 2 | a0001c0001t0002g0081a0001c0001t0006g0046 | 2 | HG01106.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.68-4806A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836099 | ||||||
| chrX:150836190
|
TG | T | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-4898delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836190 | ||||||
| chrX:150836292
|
CA | C | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-5000delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836292 | ||||||
| chrX:150836348
|
A | AT | 62 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.68-5056dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836348 | ||||||
| chrX:150836348
|
A | ATT | 2 | a0001c0001t0001g0007a0001c0002t0001g0026 | 2 | HG01109.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.68-5057_68-5056dup others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836348 | ||||||
| chrX:150836431
|
G | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.68-5138C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836431 | ||||||
| chrX:150836453
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.68-5160T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836453 | ||||||
| chrX:150836453
|
AAGT | A | 10 | a0001c0001t0001g0184a0001c0001t0004g0176a0001c0001t0006g0191others(7): Show | 10 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-5163_68-5161del others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836453 | ||||||
| chrX:150836454
|
AGT | A | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.68-5163_68-5162del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836454 | ||||||
| chrX:150836551
|
T | TC | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-5259dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836551 | ||||||
| chrX:150836876
|
C | CA | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-5584dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836876 | ||||||
| chrX:150836994
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.68-5701G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150836994 | ||||||
| chrX:150837068
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-5775G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837068 | ||||||
| chrX:150837108
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-5815G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837108 | ||||||
| chrX:150837249
|
ATTAT | A | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.68-5960_68-5957del others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837249 | ||||||
| chrX:150837252
|
A | AT | 5 | a0001c0001t0001g0077a0001c0001t0005g0202a0001c0001t0005g0203others(2): Show | 5 | HG00735.hp2 HG01934.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-5960dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837252 | ||||||
| chrX:150837252
|
AT | A | 15 | a0001c0001t0001g0075a0001c0001t0001g0187a0001c0001t0002g0138others(12): Show | 15 | HG01081.hp1 HG01517.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-5960delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837252 | ||||||
| chrX:150837272
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.68-5979C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837272 | ||||||
| chrX:150837318
|
TG | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-6026delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837318 | ||||||
| chrX:150837382
|
TG | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-6090delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837382 | ||||||
| chrX:150837560
|
TA | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-6268delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837560 | ||||||
| chrX:150837909
|
TC | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-6617delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837909 | ||||||
| chrX:150837987
|
G | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.68-6694C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837987 | ||||||
| chrX:150838035
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.68-6742C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838035 | ||||||
| chrX:150838041
|
T | TC | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-6749dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838041 | ||||||
| chrX:150838328
|
TA | T | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-7036delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838328 | ||||||
| chrX:150838391
|
T | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-7098A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838391 | ||||||
| chrX:150838459
|
TG | T | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-7167delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838459 | ||||||
| chrX:150838476
|
CT | C | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-7184delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838476 | ||||||
| chrX:150838591
|
T | TA | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-7299dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838591 | ||||||
| chrX:150838678
|
T | TA | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-7386dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838678 | ||||||
| chrX:150838678
|
TA | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 153 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.68-7386delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838678 | ||||||
| chrX:150838678
|
TAA | T | 6 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0086others(3): Show | 6 | HG01070.hp2 HG01256.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7387_68-7386del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838678 | ||||||
| chrX:150838694
|
AAG | A | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-7403_68-7402del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838694 | ||||||
| chrX:150838697
|
A | G | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-7404T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838697 | ||||||
| chrX:150838711
|
GA | G | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-7419delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838711 | ||||||
| chrX:150838812
|
TC | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-7520delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838812 | ||||||
| chrX:150838831
|
AG | A | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-7539delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838831 | ||||||
| chrX:150838853
|
C | T | 1 | a0001c0005t0001g0130 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.68-7560G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838853 | ||||||
| chrX:150838866
|
CT | C | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-7574delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838866 | ||||||
| chrX:150838898
|
T | TA | 8 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0115others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-7606dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838898 | ||||||
| chrX:150838898
|
TA | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0018others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.68-7606delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838898 | ||||||
| chrX:150838898
|
TAA | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-7607_68-7606del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838898 | ||||||
| chrX:150838916
|
AAT | A | 8 | a0001c0001t0001g0077a0001c0001t0001g0162a0001c0001t0007g0196others(5): Show | 8 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-7625_68-7624del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838916 | ||||||
| chrX:150838917
|
A | AAAT | 1 | a0001c0001t0035g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.68-7625_68-7624ins others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838917 | ||||||
| chrX:150838917
|
A | AAT | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0013g0038others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-7625_68-7624ins others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838917 | ||||||
| chrX:150838917
|
A | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0002g0013others(1): Show | 4 | HG00438.hp1 HG00642.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-7624T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838917 | ||||||
| chrX:150838917
|
AT | A | 2 | a0001c0001t0008g0161a0001c0001t0010g0179 | 2 | HG01099.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.68-7625delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838917 | ||||||
| chrX:150838917
|
ATG | A | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.68-7626_68-7625del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838917 | ||||||
| chrX:150838918
|
T | A | 9 | a0001c0001t0001g0184a0001c0001t0004g0176a0001c0001t0006g0191others(6): Show | 9 | HG00099.hp1 HG01168.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-7625A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838918 | ||||||
| chrX:150838918
|
T | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0002g0013others(6): Show | 9 | HG00438.hp1 HG00642.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-7625A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838918 | ||||||
| chrX:150838918
|
T | TG | 28 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0070others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.68-7626dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838918 | ||||||
| chrX:150838918
|
T | TGG | 2 | a0001c0001t0001g0096a0001c0001t0002g0112 | 2 | HG00738.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.68-7627_68-7626dup others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838918 | ||||||
| chrX:150838918
|
TG | T | 1 | a0001c0001t0001g0057 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.68-7626delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838918 | ||||||
| chrX:150838918
|
TGG | T | 1 | a0001c0001t0003g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.68-7627_68-7626del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838918 | ||||||
| chrX:150838919
|
G | A | 2 | a0001c0001t0008g0161a0001c0001t0010g0179 | 2 | HG01099.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.68-7626C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838919 | ||||||
| chrX:150838919
|
G | T | 17 | a0001c0001t0001g0077a0001c0001t0001g0162a0001c0001t0001g0184others(14): Show | 17 | HG00099.hp1 HG00735.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.68-7626C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838919 | ||||||
| chrX:150838920
|
G | A | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.68-7627C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838920 | ||||||
| chrX:150838920
|
G | T | 2 | a0001c0001t0008g0161a0001c0001t0010g0179 | 2 | HG01099.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.68-7627C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838920 | ||||||
| chrX:150838921
|
G | T | 3 | a0001c0001t0008g0168a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02451.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.68-7628C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838921 | ||||||
| chrX:150838963
|
A | T | 26 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0115others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-7670T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838963 | ||||||
| chrX:150839161
|
CATATA | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-7873_68-7869del others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150839161 | ||||||
| chrX:150839676
|
TG | T | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-8384delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150839676 | ||||||
| chrX:150839716
|
C | T | 1 | a0001c0001t0009g0180 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.68-8423G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150839716 | ||||||
| chrX:150839799
|
C | T | 29 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.68-8506G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150839799 | ||||||
| chrX:150839829
|
G | T | 1 | a0001c0001t0017g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.68-8536C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150839829 | ||||||
| chrX:150839878
|
T | TA | 3 | a0001c0001t0002g0138a0001c0001t0003g0098a0001c0001t0040g0006 | 3 | HG01517.hp1 HG02074.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.68-8586dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150839878 | ||||||
| chrX:150839912
|
C | T | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.68-8619G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150839912 | ||||||
| chrX:150839932
|
G | C | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-8639C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150839932 | ||||||
| chrX:150840022
|
A | G | 1 | a0001c0001t0025g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-8729T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840022 | ||||||
| chrX:150840026
|
A | AG | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-8734dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840026 | ||||||
| chrX:150840074
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.68-8781C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840074 | ||||||
| chrX:150840201
|
CAAAAAGA | C | 1 | a0001c0001t0001g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.68-8915_68-8909del others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840201 | ||||||
| chrX:150840217
|
A | AAAAG | 1 | a0001c0001t0004g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.68-8928_68-8925dup others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840217 | ||||||
| chrX:150840225
|
GAAAGAAA others(3): Show |
G | 3 | a0001c0001t0012g0146a0001c0001t0012g0207a0001c0001t0029g0116 | 3 | HG03139.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68-8942_68-8933del others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840225 | ||||||
| chrX:150840243
|
G | GA | 3 | a0001c0001t0001g0037a0001c0001t0001g0109a0001c0001t0040g0006 | 3 | NA18979.hp2 NA19075.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.68-8951dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840243 | ||||||
| chrX:150840263
|
G | GA | 1 | a0001c0001t0001g0089 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.68-8971dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840263 | ||||||
| chrX:150840271
|
G | A | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-8978C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840271 | ||||||
| chrX:150840414
|
C | CT | 24 | a0001c0001t0001g0089a0001c0001t0001g0110a0001c0001t0001g0111others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.68-9122dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840414 | ||||||
| chrX:150840414
|
CT | C | 1 | a0001c0002t0001g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-9122delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840414 | ||||||
| chrX:150840522
|
AC | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-9230delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840522 | ||||||
| chrX:150840573
|
CT | C | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-9281delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840573 | ||||||
| chrX:150840647
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.68-9354T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840647 | ||||||
| chrX:150840700
|
A | G | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.68-9407T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840700 | ||||||
| chrX:150840739
|
TGGGAC | T | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-9451_68-9447del others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840739 | ||||||
| chrX:150840876
|
ATT | A | 3 | a0001c0001t0011g0163a0001c0001t0011g0164a0001c0001t0025g0144 | 3 | HG01884.hp2 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.68-9585_68-9584del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840876 | ||||||
| chrX:150840884
|
T | TG | 1 | a0001c0001t0001g0041 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.68-9592dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840884 | ||||||
| chrX:150840932
|
TG | T | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-9640delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840932 | ||||||
| chrX:150840973
|
C | T | 1 | a0001c0001t0024g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-9680G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840973 | ||||||
| chrX:150841027
|
AC | A | 1 | a0001c0001t0040g0006 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.68-9735delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841027 | ||||||
| chrX:150841219
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 140 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.68-9926C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841219 | ||||||
| chrX:150841284
|
GA | G | 1 | a0001c0001t0003g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.68-9992delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841284 | ||||||
| chrX:150841291
|
A | AATTTTTT | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-9999_68-9998ins others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841291 | ||||||
| chrX:150841292
|
T | A | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-9999A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841292 | ||||||
| chrX:150841450
|
CT | C | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-10158delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841450 | ||||||
| chrX:150841640
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-10347G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841640 | ||||||
| chrX:150841792
|
C | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-10499G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841792 | ||||||
| chrX:150842129
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-10836C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150842129 | ||||||
| chrX:150842153
|
A | T | 2 | a0001c0001t0001g0015a0001c0002t0002g0010 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.68-10860T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150842153 | ||||||
| chrX:150842443
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.68-11150C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150842443 | ||||||
| chrX:150842510
|
G | C | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-11217C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150842510 | ||||||
| chrX:150843524
|
G | A | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.68-12231C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150843524 | ||||||
| chrX:150843712
|
A | G | 1 | a0001c0001t0038g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.68-12419T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150843712 | ||||||
| chrX:150844227
|
TC | T | 1 | a0001c0001t0021g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.68-12935delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150844227 | ||||||
| chrX:150844610
|
T | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(19): Show | 22 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.68-13317A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150844610 | ||||||
| chrX:150844623
|
T | A | 1 | a0001c0001t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.68-13330A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150844623 | ||||||
| chrX:150844742
|
A | G | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-13449T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150844742 | ||||||
| chrX:150844851
|
CCCGGTCA others(10): Show |
C | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.68-13575_68-13559d others(19): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150844851 | ||||||
| chrX:150844852
|
C | A | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68-13559G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150844852 | ||||||
| chrX:150844853
|
CGGTCACT others(10): Show |
C | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68-13577_68-13561d others(19): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150844853 | ||||||
| chrX:150844870
|
A | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.68-13577T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150844870 | ||||||
| chrX:150845251
|
T | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.68-13958A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150845251 | ||||||
| chrX:150845307
|
TG | T | 1 | a0001c0001t0006g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.68-14015delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150845307 | ||||||
| chrX:150845397
|
G | A | 1 | a0001c0001t0010g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.68-14104C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150845397 | ||||||
| chrX:150845412
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.68-14119C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150845412 | ||||||
| chrX:150845418
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.68-14125A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150845418 | ||||||
| chrX:150845576
|
A | G | 1 | a0001c0001t0011g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-14283T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150845576 | ||||||
| chrX:150845822
|
G | A | 1 | a0001c0002t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.68-14529C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150845822 | ||||||
| chrX:150845989
|
G | A | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.68-14696C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150845989 | ||||||
| chrX:150846068
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-14775G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150846068 | ||||||
| chrX:150847277
|
GT | G | 1 | a0001c0001t0001g0126 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.68-15985delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150847277 | ||||||
| chrX:150847435
|
T | C | 2 | a0001c0001t0018g0104a0001c0001t0018g0105 | 2 | NA18945.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.68-16142A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150847435 | ||||||
| chrX:150847551
|
TC | T | 1 | a0001c0001t0001g0033 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.68-16259delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150847551 | ||||||
| chrX:150847847
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.68-16554T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150847847 | ||||||
| chrX:150848111
|
G | GC | 63 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.68-16819dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848111 | ||||||
| chrX:150848111
|
G | GCC | 14 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0186others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-16820_68-16819d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848111 | ||||||
| chrX:150848111
|
G | GCCC | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0006g0191others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-16821_68-16819d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848111 | ||||||
| chrX:150848118
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-16825G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848118 | ||||||
| chrX:150848120
|
C | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0124 | 2 | NA18747.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.68-16827G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848120 | ||||||
| chrX:150848121
|
C | CG | 1 | a0001c0001t0038g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.68-16829_68-16828i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848121 | ||||||
| chrX:150848328
|
G | A | 5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-17035C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848328 | ||||||
| chrX:150848404
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0008g0161a0001c0001t0008g0168others(2): Show | 5 | HG01884.hp1 HG02451.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-17111C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848404 | ||||||
| chrX:150848556
|
T | TA | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 136 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.68-17264dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848556 | ||||||
| chrX:150848556
|
T | TAA | 2 | a0001c0001t0001g0033a0001c0001t0001g0102 | 2 | NA18977.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.68-17265_68-17264d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848556 | ||||||
| chrX:150848556
|
TA | T | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68-17264delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848556 | ||||||
| chrX:150848556
|
TAA | T | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-17265_68-17264d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848556 | ||||||
| chrX:150848556
|
TAAA | T | 1 | a0001c0001t0006g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.68-17266_68-17264d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848556 | ||||||
| chrX:150849077
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 89 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.68-17784G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150849077 | ||||||
| chrX:150849087
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.68-17794G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150849087 | ||||||
| chrX:150849112
|
T | G | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-17819A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150849112 | ||||||
| chrX:150849636
|
C | T | 2 | a0001c0001t0009g0195a0001c0001t0017g0194 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.68-18343G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150849636 | ||||||
| chrX:150850184
|
T | C | 1 | a0001c0001t0004g0047 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.68-18891A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150850184 | ||||||
| chrX:150850480
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.68-19187G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150850480 | ||||||
| chrX:150850663
|
T | C | 1 | a0001c0001t0030g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.68-19370A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150850663 | ||||||
| chrX:150850775
|
T | C | 6 | a0001c0001t0001g0134a0001c0001t0002g0039a0001c0001t0002g0042others(3): Show | 6 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-19482A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150850775 | ||||||
| chrX:150850838
|
C | CT | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68-19546dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150850838 | ||||||
| chrX:150850914
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0019g0174 | 2 | NA19043.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.68-19621G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150850914 | ||||||
| chrX:150850985
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68-19692C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150850985 | ||||||
| chrX:150851218
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.68-19925G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150851218 | ||||||
| chrX:150851308
|
A | G | 2 | a0001c0001t0005g0133a0001c0001t0038g0136 | 2 | HG01255.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.68-20015T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150851308 | ||||||
| chrX:150851342
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.68-20049G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150851342 | ||||||
| chrX:150851533
|
G | A | 45 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.68-20240C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150851533 | ||||||
| chrX:150852439
|
C | A | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-21146G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150852439 | ||||||
| chrX:150852633
|
C | T | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-21340G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150852633 | ||||||
| chrX:150852654
|
T | C | 1 | a0001c0001t0010g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.68-21361A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150852654 | ||||||
| chrX:150852665
|
A | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-21372T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150852665 | ||||||
| chrX:150852894
|
A | G | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-21601T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150852894 | ||||||
| chrX:150853018
|
G | T | 17 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-21725C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150853018 | ||||||
| chrX:150853022
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-21729A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150853022 | ||||||
| chrX:150853328
|
G | C | 2 | a0001c0001t0002g0017a0001c0001t0035g0167 | 2 | HG01934.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.68-22035C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150853328 | ||||||
| chrX:150853688
|
A | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.68-22395T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150853688 | ||||||
| chrX:150854223
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0131 | 2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.68-22930G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150854223 | ||||||
| chrX:150854891
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0053 | 2 | HG02056.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.68-23598C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150854891 | ||||||
| chrX:150854907
|
C | A | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68-23614G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150854907 | ||||||
| chrX:150855142
|
TC | T | 1 | a0001c0001t0001g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.68-23850delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150855142 | ||||||
| chrX:150855511
|
T | C | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-24218A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150855511 | ||||||
| chrX:150855893
|
A | G | 1 | a0001c0001t0036g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.68-24600T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150855893 | ||||||
| chrX:150856038
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-24745G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856038 | ||||||
| chrX:150856477
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-25184G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856477 | ||||||
| chrX:150856569
|
A | AAAT | 3 | a0001c0001t0001g0057a0001c0001t0001g0206a0001c0002t0001g0201 | 3 | HG03516.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.68-25279_68-25277d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856569 | ||||||
| chrX:150856569
|
A | AAATAAT | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167 | 3 | HG01934.hp1 HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.68-25282_68-25277d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856569 | ||||||
| chrX:150856569
|
A | AAATAATA others(2): Show |
13 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0002g0081others(10): Show | 13 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-25285_68-25277d others(11): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856569 | ||||||
| chrX:150856569
|
AAAT | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.68-25279_68-25277d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856569 | ||||||
| chrX:150856569
|
AAATAAT | A | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-25282_68-25277d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856569 | ||||||
| chrX:150856569
|
AAATAATA others(5): Show |
A | 1 | a0001c0001t0001g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-25288_68-25277d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856569 | ||||||
| chrX:150856706
|
T | C | 17 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-25413A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856706 | ||||||
| chrX:150856937
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-25644A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150856937 | ||||||
| chrX:150857029
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.68-25736A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150857029 | ||||||
| chrX:150857219
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-25926G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150857219 | ||||||
| chrX:150857486
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01070.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.68-26193G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150857486 | ||||||
| chrX:150857579
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0155a0001c0001t0041g0208 | 3 | HG00438.hp2 HG02040.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.68-26286G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150857579 | ||||||
| chrX:150858288
|
C | T | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-26995G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150858288 | ||||||
| chrX:150858410
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-27117G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150858410 | ||||||
| chrX:150858437
|
A | G | 1 | a0001c0001t0005g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.68-27144T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150858437 | ||||||
| chrX:150858960
|
T | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0094others(3): Show | 6 | HG00408.hp2 HG00673.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-27667A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150858960 | ||||||
| chrX:150859015
|
AG | A | 1 | a0001c0001t0001g0126 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.68-27723delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859015 | ||||||
| chrX:150859021
|
CA | C | 1 | a0001c0001t0001g0126 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.68-27729delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859021 | ||||||
| chrX:150859109
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.68-27816T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859109 | ||||||
| chrX:150859342
|
T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-28049A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859342 | ||||||
| chrX:150859391
|
CG | C | 1 | a0001c0001t0001g0126 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.68-28099delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859391 | ||||||
| chrX:150859499
|
CT | C | 46 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0115others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.68-28207delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859499 | ||||||
| chrX:150859499
|
CTT | C | 2 | a0001c0001t0004g0122a0003c0004t0042g0209 | 2 | HG01168.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.68-28208_68-28207d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859499 | ||||||
| chrX:150859499
|
CTTTTTTT others(1): Show |
C | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-28214_68-28207d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859499 | ||||||
| chrX:150859503
|
T | C | 1 | a0001c0001t0004g0122 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.68-28210A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859503 | ||||||
| chrX:150859689
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-28396C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859689 | ||||||
| chrX:150859771
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-28478A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859771 | ||||||
| chrX:150859794
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-28501G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859794 | ||||||
| chrX:150859965
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.68-28672G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859965 | ||||||
| chrX:150859983
|
G | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-28690C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150859983 | ||||||
| chrX:150860258
|
T | TA | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.68-28966dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150860258 | ||||||
| chrX:150860261
|
T | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.68-28968A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150860261 | ||||||
| chrX:150860280
|
TG | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.68-28988delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150860280 | ||||||
| chrX:150860317
|
GT | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.68-29025delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150860317 | ||||||
| chrX:150860388
|
A | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-29095T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150860388 | ||||||
| chrX:150860992
|
A | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-29699T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150860992 | ||||||
| chrX:150861141
|
C | CA | 3 | a0001c0001t0001g0077a0001c0001t0001g0193a0001c0001t0044g0210 | 3 | HG00735.hp2 HG01243.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.68-29849dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
C | CAA | 7 | a0001c0001t0001g0162a0001c0001t0002g0107a0001c0001t0008g0161others(4): Show | 7 | HG01258.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-29850_68-29849d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
C | CAAAAA | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(16): Show | 19 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-29853_68-29849d others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
C | CAAAAAA | 2 | a0001c0001t0001g0015a0001c0002t0001g0026 | 2 | NA18981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.68-29854_68-29849d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0134a0001c0001t0009g0195a0001c0001t0017g0194others(1): Show | 4 | HG00323.hp2 HG02647.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-29862_68-29849d others(16): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
C | CAAAAAAA others(8): Show |
12 | a0001c0001t0001g0111a0001c0001t0002g0039a0001c0001t0002g0112others(9): Show | 12 | HG00280.hp1 HG00738.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-29863_68-29849d others(17): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0002g0042a0001c0001t0007g0196a0001c0001t0007g0197others(2): Show | 5 | HG00741.hp2 HG02145.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-29864_68-29849d others(18): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
C | CAAAAAAA others(10): Show |
5 | a0001c0001t0001g0110a0001c0001t0006g0044a0001c0001t0013g0038others(2): Show | 5 | HG00099.hp2 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-29865_68-29849d others(19): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-29849_68-29848i others(27): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861141
|
CA | C | 13 | a0001c0001t0001g0126a0001c0001t0001g0184a0001c0001t0001g0186others(10): Show | 13 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-29849delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861141 | ||||||
| chrX:150861158
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.68-29865T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861158 | ||||||
| chrX:150861566
|
T | C | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-30273A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861566 | ||||||
| chrX:150861626
|
G | A | 5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-30333C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861626 | ||||||
| chrX:150861872
|
C | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-30579G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861872 | ||||||
| chrX:150861889
|
G | C | 1 | a0001c0001t0007g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-30596C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861889 | ||||||
| chrX:150861905
|
C | CA | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-30613dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861905 | ||||||
| chrX:150861905
|
CA | C | 6 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0155others(3): Show | 6 | HG02083.hp1 HG02895.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-30613delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861905 | ||||||
| chrX:150861916
|
AAAG | A | 1 | a0001c0001t0005g0202 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.68-30626_68-30624d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861916 | ||||||
| chrX:150861917
|
A | AG | 1 | a0001c0001t0001g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.68-30625_68-30624i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861917 | ||||||
| chrX:150861917
|
AAG | A | 3 | a0001c0001t0005g0203a0001c0001t0035g0167a0001c0002t0001g0201 | 3 | HG01934.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.68-30626_68-30625d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861917 | ||||||
| chrX:150861917
|
AAGAG | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-30628_68-30625d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861917 | ||||||
| chrX:150861918
|
AGAG | A | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68-30628_68-30626d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861918 | ||||||
| chrX:150861935
|
G | C | 1 | a0001c0002t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.68-30642C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861935 | ||||||
| chrX:150862035
|
C | A | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-30742G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862035 | ||||||
| chrX:150862040
|
T | A | 45 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.68-30747A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862040 | ||||||
| chrX:150862170
|
A | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.68-30877T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862170 | ||||||
| chrX:150862288
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.68-30995G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862288 | ||||||
| chrX:150862526
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.68-31233T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862526 | ||||||
| chrX:150862836
|
A | AAG | 9 | a0001c0001t0002g0017a0001c0001t0005g0202a0001c0001t0005g0203others(6): Show | 9 | HG01934.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-31545_68-31544d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862836 | ||||||
| chrX:150862836
|
A | AG | 1 | a0001c0001t0012g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-31544_68-31543i others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862836 | ||||||
| chrX:150862850
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-31557C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862850 | ||||||
| chrX:150862854
|
GAC | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-31563_68-31562d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862854 | ||||||
| chrX:150862862
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-31569C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862862 | ||||||
| chrX:150862868
|
GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0001g0063 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.68-31585_68-31576d others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862868 | ||||||
| chrX:150862876
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-31583C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862876 | ||||||
| chrX:150862878
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-31585T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862878 | ||||||
| chrX:150862886
|
G | GAAAAGA | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-31594_68-31593i others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862886 | ||||||
| chrX:150862886
|
G | GAAAGA | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-31598_68-31594d others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862886 | ||||||
| chrX:150862886
|
G | GAAAGAAA others(3): Show |
57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.68-31603_68-31594d others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862886 | ||||||
| chrX:150862886
|
G | GAAAGAAA others(8): Show |
3 | a0001c0001t0001g0110a0001c0001t0006g0044a0001c0001t0009g0189 | 3 | HG00099.hp2 HG01081.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.68-31608_68-31594d others(17): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862886 | ||||||
| chrX:150862956
|
C | T | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-31663G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862956 | ||||||
| chrX:150862999
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.68-31706G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862999 | ||||||
| chrX:150863587
|
G | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-32294C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150863587 | ||||||
| chrX:150864173
|
T | C | 1 | a0001c0001t0015g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.68-32880A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150864173 | ||||||
| chrX:150864287
|
G | C | 1 | a0001c0001t0024g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-32994C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150864287 | ||||||
| chrX:150864466
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-33173A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150864466 | ||||||
| chrX:150864657
|
G | A | 1 | a0001c0001t0011g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-33364C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150864657 | ||||||
| chrX:150864863
|
C | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-33570G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150864863 | ||||||
| chrX:150865066
|
C | CA | 12 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0186others(9): Show | 12 | HG01074.hp1 HG01928.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+33455dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150865066 | ||||||
| chrX:150865066
|
C | CAA | 1 | a0001c0001t0008g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+33454_67+33455d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150865066 | ||||||
| chrX:150865496
|
AATAG | A | 1 | a0001c0001t0017g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+33022_67+33025d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150865496 | ||||||
| chrX:150865964
|
T | C | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+32558A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150865964 | ||||||
| chrX:150866291
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+32231T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866291 | ||||||
| chrX:150866302
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.67+32220G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866302 | ||||||
| chrX:150866570
|
TA | T | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+31951delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866570 | ||||||
| chrX:150866615
|
G | T | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+31907C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866615 | ||||||
| chrX:150866625
|
G | A | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+31897C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866625 | ||||||
| chrX:150866655
|
C | T | 1 | a0001c0001t0011g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67+31867G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866655 | ||||||
| chrX:150866816
|
A | AC | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.67+31705dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866816 | ||||||
| chrX:150866959
|
G | GA | 1 | a0001c0001t0005g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+31562dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866959 | ||||||
| chrX:150867011
|
GT | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+31510delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867011 | ||||||
| chrX:150867077
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0008g0139 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+31445C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867077 | ||||||
| chrX:150867440
|
A | G | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+31082T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867440 | ||||||
| chrX:150867641
|
C | T | 5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+30881G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867641 | ||||||
| chrX:150867808
|
G | A | 1 | a0001c0001t0010g0185 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67+30714C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867808 | ||||||
| chrX:150867892
|
C | CA | 1 | a0001c0001t0003g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.67+30629dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867892 | ||||||
| chrX:150867892
|
CA | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0018others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.67+30629delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867892 | ||||||
| chrX:150867892
|
CAA | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(29): Show | 32 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+30628_67+30629d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867892 | ||||||
| chrX:150867892
|
CAAA | C | 11 | a0001c0001t0001g0115a0001c0001t0001g0184a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+30627_67+30629d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867892 | ||||||
| chrX:150867892
|
CAAAA | C | 3 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0002t0001g0173 | 3 | HG02451.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.67+30626_67+30629d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867892 | ||||||
| chrX:150867892
|
CAAAAAAA | C | 1 | a0001c0001t0019g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.67+30623_67+30629d others(9): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867892 | ||||||
| chrX:150867892
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0037g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.67+30616_67+30629d others(16): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867892 | ||||||
| chrX:150868084
|
A | AAAT | 15 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0043others(12): Show | 16 | HG00741.hp1 HG01069.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+30435_67+30437d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868084 | ||||||
| chrX:150868084
|
A | AAATAAT | 3 | a0001c0001t0001g0089a0001c0001t0005g0200a0001c0001t0020g0060 | 3 | HG03130.hp1 NA18953.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.67+30432_67+30437d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868084 | ||||||
| chrX:150868084
|
AAAT | A | 10 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0123others(7): Show | 10 | HG01516.hp2 HG01884.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+30435_67+30437d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868084 | ||||||
| chrX:150868084
|
AAATAAT | A | 28 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0034others(25): Show | 28 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.67+30432_67+30437d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868084 | ||||||
| chrX:150868084
|
AAATAATA others(2): Show |
A | 52 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.67+30429_67+30437d others(11): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868084 | ||||||
| chrX:150868133
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+30389A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868133 | ||||||
| chrX:150868420
|
C | T | 5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+30102G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868420 | ||||||
| chrX:150868510
|
A | G | 1 | a0001c0001t0037g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.67+30012T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868510 | ||||||
| chrX:150868625
|
C | A | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+29897G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868625 | ||||||
| chrX:150868700
|
T | C | 1 | a0001c0001t0010g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.67+29822A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868700 | ||||||
| chrX:150868703
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.67+29819C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868703 | ||||||
| chrX:150868911
|
G | A | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+29611C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868911 | ||||||
| chrX:150868966
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.67+29556A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150868966 | ||||||
| chrX:150869031
|
T | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+29491A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150869031 | ||||||
| chrX:150869204
|
A | C | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+29318T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150869204 | ||||||
| chrX:150869489
|
T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+29033A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150869489 | ||||||
| chrX:150869508
|
T | C | 4 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0035g0167others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+29014A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150869508 | ||||||
| chrX:150869684
|
G | A | 3 | a0001c0001t0004g0176a0001c0001t0011g0171a0001c0001t0026g0149 | 3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.67+28838C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150869684 | ||||||
| chrX:150869910
|
GA | G | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+28611delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150869910 | ||||||
| chrX:150870048
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.67+28474C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150870048 | ||||||
| chrX:150870087
|
C | A | 17 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+28435G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150870087 | ||||||
| chrX:150870567
|
A | G | 1 | a0001c0001t0044g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.67+27955T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150870567 | ||||||
| chrX:150870581
|
C | A | 1 | a0002c0003t0012g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.67+27941G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150870581 | ||||||
| chrX:150870811
|
G | C | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+27711C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150870811 | ||||||
| chrX:150870960
|
G | A | 4 | a0001c0001t0009g0147a0001c0001t0012g0146a0001c0001t0012g0207others(1): Show | 4 | HG03139.hp1 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+27562C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150870960 | ||||||
| chrX:150871044
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+27478C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150871044 | ||||||
| chrX:150871101
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.67+27421T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150871101 | ||||||
| chrX:150871279
|
C | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+27243G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150871279 | ||||||
| chrX:150871863
|
T | C | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+26659A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150871863 | ||||||
| chrX:150871964
|
G | A | 1 | a0001c0002t0001g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+26558C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150871964 | ||||||
| chrX:150871973
|
G | A | 1 | a0001c0001t0011g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67+26549C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150871973 | ||||||
| chrX:150872057
|
C | A | 1 | a0001c0001t0030g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.67+26465G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872057 | ||||||
| chrX:150872085
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+26437C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872085 | ||||||
| chrX:150872241
|
A | G | 4 | a0001c0001t0001g0193a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+26281T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872241 | ||||||
| chrX:150872244
|
C | CA | 1 | a0001c0001t0011g0164 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.67+26277dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872244 | ||||||
| chrX:150872360
|
T | G | 1 | a0001c0001t0001g0040 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.67+26162A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872360 | ||||||
| chrX:150872453
|
C | CA | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+26068dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872453 | ||||||
| chrX:150872542
|
T | TA | 22 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0037others(19): Show | 22 | HG00408.hp1 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.67+25979dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872542 | ||||||
| chrX:150872542
|
T | TAA | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(11): Show | 14 | HG00438.hp1 HG01070.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+25978_67+25979d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872542 | ||||||
| chrX:150872542
|
T | TAAA | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+25977_67+25979d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872542 | ||||||
| chrX:150872542
|
T | TAAAA | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.67+25976_67+25979d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872542 | ||||||
| chrX:150872661
|
TA | T | 25 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0058others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.67+25860delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872661 | ||||||
| chrX:150872676
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+25846G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872676 | ||||||
| chrX:150872818
|
G | T | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+25704C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872818 | ||||||
| chrX:150872852
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0056a0001c0001t0001g0101others(1): Show | 4 | NA18944.hp1 NA18981.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+25670C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150872852 | ||||||
| chrX:150873073
|
T | G | 4 | a0001c0001t0001g0193a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+25449A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150873073 | ||||||
| chrX:150873189
|
G | C | 4 | a0001c0001t0001g0193a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+25333C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150873189 | ||||||
| chrX:150873324
|
C | T | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+25198G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150873324 | ||||||
| chrX:150873343
|
A | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+25179T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150873343 | ||||||
| chrX:150873589
|
AT | A | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.67+24932delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150873589 | ||||||
| chrX:150873738
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67+24784T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150873738 | ||||||
| chrX:150874149
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+24373A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150874149 | ||||||
| chrX:150874170
|
C | T | 3 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0014g0172 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.67+24352G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150874170 | ||||||
| chrX:150874421
|
A | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+24101T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150874421 | ||||||
| chrX:150874559
|
GGGGGGC | G | 1 | a0001c0001t0003g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.67+23957_67+23962d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150874559 | ||||||
| chrX:150874565
|
C | CG | 1 | a0001c0001t0039g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67+23956dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150874565 | ||||||
| chrX:150874571
|
C | CG | 3 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0020g0025 | 3 | NA18967.hp1 NA19000.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.67+23950dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150874571 | ||||||
| chrX:150875096
|
T | C | 2 | a0001c0001t0021g0117a0001c0001t0021g0150 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.67+23426A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875096 | ||||||
| chrX:150875150
|
T | A | 1 | a0001c0001t0023g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.67+23372A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875150 | ||||||
| chrX:150875277
|
A | G | 1 | a0001c0001t0019g0178 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67+23245T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875277 | ||||||
| chrX:150875383
|
T | C | 1 | a0001c0001t0002g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.67+23139A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875383 | ||||||
| chrX:150875616
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0002g0039a0001c0001t0002g0042others(3): Show | 6 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+22906C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875616 | ||||||
| chrX:150875648
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+22874G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875648 | ||||||
| chrX:150875683
|
T | G | 4 | a0001c0001t0001g0193a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+22839A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875683 | ||||||
| chrX:150875784
|
A | C | 1 | a0001c0001t0016g0073 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.67+22738T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875784 | ||||||
| chrX:150875812
|
CTT | C | 19 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.67+22708_67+22709d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150875812 | ||||||
| chrX:150876440
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+22082T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150876440 | ||||||
| chrX:150877121
|
T | TA | 34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.67+21400dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877121 | ||||||
| chrX:150877121
|
T | TAA | 28 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.67+21399_67+21400d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877121 | ||||||
| chrX:150877121
|
TA | T | 1 | a0001c0001t0021g0150 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.67+21400delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877121 | ||||||
| chrX:150877134
|
A | G | 1 | a0001c0001t0009g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.67+21388T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877134 | ||||||
| chrX:150877330
|
G | A | 1 | a0001c0001t0003g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.67+21192C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877330 | ||||||
| chrX:150877354
|
T | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.67+21168A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877354 | ||||||
| chrX:150877427
|
C | CAG | 1 | a0002c0003t0012g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.67+21093_67+21094d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877427 | ||||||
| chrX:150877600
|
T | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.67+20922A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877600 | ||||||
| chrX:150877677
|
G | A | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+20845C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877677 | ||||||
| chrX:150877721
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+20801G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877721 | ||||||
| chrX:150877895
|
T | C | 1 | a0001c0001t0006g0046 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.67+20627A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877895 | ||||||
| chrX:150877959
|
T | TAC | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(17): Show | 20 | HG01258.hp1 HG01261.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+20561_67+20562d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
T | TACAC | 20 | a0001c0001t0001g0037a0001c0001t0001g0175a0001c0001t0001g0183others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+20559_67+20562d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
T | TACACAC | 10 | a0001c0001t0001g0193a0001c0001t0002g0012a0001c0001t0002g0013others(7): Show | 10 | HG00642.hp1 HG01192.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+20557_67+20562d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0102a0001c0001t0007g0196a0001c0001t0009g0195others(1): Show | 4 | HG02145.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+20555_67+20562d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
T | TACACACA others(5): Show |
1 | a0001c0001t0035g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.67+20551_67+20562d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
T | TCACAC | 1 | a0001c0001t0017g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67+20562_67+20563i others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
TAC | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.67+20561_67+20562d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
TACA | T | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.67+20560_67+20562d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
TACAC | T | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0106others(8): Show | 11 | HG00621.hp1 HG00673.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+20559_67+20562d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
TACACAC | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+20557_67+20562d others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0017g0020a0001c0001t0030g0045a0001c0001t0040g0006 | 3 | HG02965.hp1 HG03654.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.67+20555_67+20562d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0004g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.67+20549_67+20562d others(16): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877959
|
TACACACA others(17): Show |
T | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+20539_67+20562d others(26): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877959 | ||||||
| chrX:150877986
|
A | AC | 1 | a0001c0002t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.67+20535dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150877986 | ||||||
| chrX:150878337
|
T | TA | 1 | a0001c0001t0011g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67+20184dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878337 | ||||||
| chrX:150878533
|
T | TA | 2 | a0001c0001t0001g0032a0001c0001t0043g0211 | 2 | NA19005.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.67+19988dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878533 | ||||||
| chrX:150878533
|
T | TAA | 6 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0008g0161others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+19987_67+19988d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878533 | ||||||
| chrX:150878533
|
T | TAAA | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+19986_67+19988d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878533 | ||||||
| chrX:150878533
|
TA | T | 11 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0192others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+19988delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878533 | ||||||
| chrX:150878618
|
G | C | 8 | a0001c0001t0001g0193a0001c0001t0005g0202a0001c0001t0005g0203others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+19904C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878618 | ||||||
| chrX:150878625
|
G | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+19897C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878625 | ||||||
| chrX:150878630
|
C | T | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+19892G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878630 | ||||||
| chrX:150878812
|
C | A | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.67+19710G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878812 | ||||||
| chrX:150878842
|
C | T | 1 | a0001c0001t0039g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67+19680G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150878842 | ||||||
| chrX:150879196
|
T | C | 1 | a0001c0001t0011g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67+19326A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879196 | ||||||
| chrX:150879205
|
G | T | 1 | a0001c0001t0017g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+19317C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879205 | ||||||
| chrX:150879377
|
T | C | 4 | a0001c0001t0001g0193a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+19145A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879377 | ||||||
| chrX:150879404
|
T | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(8): Show | 11 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+19118A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879404 | ||||||
| chrX:150879413
|
T | C | 1 | a0001c0001t0008g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67+19109A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879413 | ||||||
| chrX:150879516
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0008g0161a0001c0001t0008g0168others(2): Show | 5 | HG01884.hp1 HG02451.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+19006C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879516 | ||||||
| chrX:150879550
|
A | C | 9 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0005g0202others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+18972T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879550 | ||||||
| chrX:150879693
|
G | A | 1 | a0001c0001t0035g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.67+18829C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879693 | ||||||
| chrX:150879750
|
T | TA | 33 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0062others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.67+18771dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
T | TAA | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+18770_67+18771d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
T | TAAA | 8 | a0001c0001t0001g0037a0001c0001t0002g0012a0001c0001t0002g0013others(5): Show | 8 | HG00642.hp1 HG01192.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+18769_67+18771d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
T | TAAAA | 3 | a0001c0001t0011g0171a0001c0001t0017g0194a0001c0001t0036g0145 | 3 | HG02647.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.67+18768_67+18771d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
T | TTA | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+18771_67+18772i others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
T | TTAA | 8 | a0001c0001t0001g0184a0001c0001t0004g0176a0001c0001t0006g0191others(5): Show | 8 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+18771_67+18772i others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
T | TTAAA | 1 | a0001c0001t0010g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.67+18771_67+18772i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
T | TTAAAA | 1 | a0001c0001t0024g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67+18771_67+18772i others(7): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
TA | T | 10 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG00323.hp1 HG01070.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+18771delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
TAAA | T | 2 | a0001c0001t0008g0168a0001c0002t0001g0173 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.67+18769_67+18771d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879750
|
TAAAA | T | 3 | a0001c0001t0001g0115a0001c0001t0008g0161a0001c0001t0019g0174 | 3 | HG01884.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.67+18768_67+18771d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879750 | ||||||
| chrX:150879783
|
G | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0176others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+18739C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879783 | ||||||
| chrX:150879793
|
T | C | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67+18729A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879793 | ||||||
| chrX:150879925
|
C | CA | 14 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0055others(11): Show | 14 | HG00642.hp1 HG01884.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+18596dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879925 | ||||||
| chrX:150879925
|
C | CAA | 1 | a0001c0001t0001g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.67+18595_67+18596d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879925 | ||||||
| chrX:150879925
|
C | CAAA | 6 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0008g0161others(3): Show | 6 | HG02258.hp1 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+18594_67+18596d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879925 | ||||||
| chrX:150879925
|
C | CAAAA | 2 | a0001c0001t0001g0193a0001c0002t0001g0201 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+18593_67+18596d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879925 | ||||||
| chrX:150879925
|
CA | C | 4 | a0001c0001t0001g0114a0001c0001t0014g0159a0001c0001t0014g0160others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+18596delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150879925 | ||||||
| chrX:150880256
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.67+18266T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880256 | ||||||
| chrX:150880301
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+18221A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880301 | ||||||
| chrX:150880327
|
C | T | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198 | 3 | HG02145.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.67+18195G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880327 | ||||||
| chrX:150880330
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+18192A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880330 | ||||||
| chrX:150880430
|
T | G | 2 | a0001c0001t0001g0015a0001c0002t0002g0010 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.67+18092A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880430 | ||||||
| chrX:150880543
|
G | A | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+17979C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880543 | ||||||
| chrX:150880767
|
G | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.67+17755C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880767 | ||||||
| chrX:150880841
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.67+17681A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880841 | ||||||
| chrX:150880916
|
T | C | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+17606A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150880916 | ||||||
| chrX:150881019
|
A | G | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.67+17503T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881019 | ||||||
| chrX:150881060
|
A | G | 1 | a0001c0001t0002g0016 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.67+17462T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881060 | ||||||
| chrX:150881112
|
T | G | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.67+17410A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881112 | ||||||
| chrX:150881156
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.67+17366G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881156 | ||||||
| chrX:150881358
|
C | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.67+17164G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881358 | ||||||
| chrX:150881445
|
T | C | 17 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0057others(14): Show | 17 | HG02027.hp1 HG02074.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.67+17077A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881445 | ||||||
| chrX:150881540
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+16982A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881540 | ||||||
| chrX:150881806
|
C | CAATT | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+16715_67+16716i others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881806 | ||||||
| chrX:150881808
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+16714G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881808 | ||||||
| chrX:150881815
|
A | AT | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(32): Show | 35 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.67+16706dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881815 | ||||||
| chrX:150881815
|
A | ATT | 3 | a0001c0001t0007g0196a0001c0001t0028g0074a0001c0001t0037g0143 | 3 | HG02145.hp1 HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.67+16705_67+16706d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881815 | ||||||
| chrX:150881815
|
A | ATTT | 2 | a0001c0001t0001g0193a0001c0001t0004g0088 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.67+16704_67+16706d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881815 | ||||||
| chrX:150881815
|
AT | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0126a0001c0001t0001g0134others(6): Show | 9 | HG00323.hp1 HG00323.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+16706delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881815 | ||||||
| chrX:150881815
|
ATT | A | 1 | a0003c0004t0042g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.67+16705_67+16706d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881815 | ||||||
| chrX:150881844
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+16678C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881844 | ||||||
| chrX:150881905
|
C | G | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.67+16617G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881905 | ||||||
| chrX:150882558
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+15964G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150882558 | ||||||
| chrX:150882742
|
T | TAAGGTTA others(23): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0193 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.67+15779_67+15780i others(32): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150882742 | ||||||
| chrX:150882893
|
C | T | 3 | a0001c0001t0011g0163a0001c0001t0011g0164a0001c0001t0025g0144 | 3 | HG01884.hp2 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.67+15629G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150882893 | ||||||
| chrX:150882946
|
C | T | 52 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.67+15576G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150882946 | ||||||
| chrX:150882969
|
C | T | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+15553G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150882969 | ||||||
| chrX:150882996
|
A | AC | 2 | a0001c0001t0001g0115a0001c0001t0001g0193 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.67+15525dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150882996 | ||||||
| chrX:150883063
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67+15459C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883063 | ||||||
| chrX:150883085
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0193 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.67+15437T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883085 | ||||||
| chrX:150883427
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+15095T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883427 | ||||||
| chrX:150883440
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+15082T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883440 | ||||||
| chrX:150883533
|
G | C | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+14989C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883533 | ||||||
| chrX:150883552
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+14970T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883552 | ||||||
| chrX:150883641
|
T | G | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+14881A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883641 | ||||||
| chrX:150883672
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.67+14850A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883672 | ||||||
| chrX:150883703
|
C | CA | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.67+14818dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883703 | ||||||
| chrX:150883715
|
T | C | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67+14807A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883715 | ||||||
| chrX:150883979
|
CACA | C | 2 | a0001c0001t0001g0061a0001c0001t0004g0088 | 2 | HG01256.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.67+14540_67+14542d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883979 | ||||||
| chrX:150884012
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.67+14510A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150884012 | ||||||
| chrX:150884080
|
A | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+14442T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150884080 | ||||||
| chrX:150884259
|
T | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.67+14263A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150884259 | ||||||
| chrX:150884340
|
C | T | 1 | a0001c0001t0013g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.67+14182G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150884340 | ||||||
| chrX:150884944
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+13578G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150884944 | ||||||
| chrX:150884964
|
T | C | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.67+13558A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150884964 | ||||||
| chrX:150885082
|
CAT | C | 2 | a0001c0001t0012g0207a0001c0001t0029g0116 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.67+13438_67+13439d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885082 | ||||||
| chrX:150885330
|
C | G | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+13192G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885330 | ||||||
| chrX:150885358
|
TACAAAAA others(10): Show |
T | 5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+13147_67+13163d others(19): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885358 | ||||||
| chrX:150885365
|
AAAC | A | 2 | a0001c0001t0021g0117a0001c0001t0021g0150 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.67+13154_67+13156d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885365 | ||||||
| chrX:150885382
|
A | C | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+13140T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885382 | ||||||
| chrX:150885382
|
AAAC | A | 1 | a0001c0001t0001g0154 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.67+13137_67+13139d others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885382 | ||||||
| chrX:150885492
|
G | A | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+13030C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885492 | ||||||
| chrX:150885513
|
G | A | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+13009C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885513 | ||||||
| chrX:150885583
|
C | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+12939G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150885583 | ||||||
| chrX:150886296
|
A | T | 6 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+12226T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886296 | ||||||
| chrX:150886309
|
A | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.67+12213T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886309 | ||||||
| chrX:150886312
|
A | G | 1 | a0001c0001t0019g0178 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67+12210T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886312 | ||||||
| chrX:150886432
|
T | C | 6 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+12090A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886432 | ||||||
| chrX:150886600
|
T | C | 6 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0192others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+11922A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886600 | ||||||
| chrX:150886656
|
C | CA | 4 | a0001c0001t0002g0140a0001c0001t0008g0139a0001c0001t0016g0072others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+11865dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886656 | ||||||
| chrX:150886693
|
T | C | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67+11829A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886693 | ||||||
| chrX:150886726
|
C | T | 1 | a0001c0002t0001g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.67+11796G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886726 | ||||||
| chrX:150886904
|
T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.67+11618A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886904 | ||||||
| chrX:150886938
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.67+11584C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150886938 | ||||||
| chrX:150887048
|
C | G | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.67+11474G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887048 | ||||||
| chrX:150887141
|
C | CA | 6 | a0001c0001t0001g0001a0001c0001t0004g0199a0001c0001t0005g0202others(3): Show | 7 | HG00741.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+11380dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887141 | ||||||
| chrX:150887141
|
C | CAA | 6 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+11379_67+11380d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887141 | ||||||
| chrX:150887141
|
CA | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.67+11380delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887141 | ||||||
| chrX:150887141
|
CAA | C | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+11379_67+11380d others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887141 | ||||||
| chrX:150887283
|
T | C | 1 | a0001c0001t0003g0127 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.67+11239A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887283 | ||||||
| chrX:150887321
|
C | T | 1 | a0001c0001t0005g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67+11201G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887321 | ||||||
| chrX:150887376
|
G | T | 1 | a0001c0001t0017g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+11146C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887376 | ||||||
| chrX:150887389
|
C | T | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+11133G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887389 | ||||||
| chrX:150887407
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67+11115G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887407 | ||||||
| chrX:150887442
|
G | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.67+11080C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887442 | ||||||
| chrX:150887447
|
C | CAGAA | 1 | a0001c0001t0035g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.67+11071_67+11074d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887447 | ||||||
| chrX:150887449
|
G | GAAAT | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.67+11069_67+11072d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887449 | ||||||
| chrX:150887449
|
G | GAAATAAA others(1): Show |
18 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0037others(15): Show | 18 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.67+11065_67+11072d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887449 | ||||||
| chrX:150887449
|
G | GAAATAAA others(5): Show |
8 | a0001c0001t0001g0162a0001c0001t0001g0186a0001c0001t0004g0176others(5): Show | 8 | HG02055.hp1 HG02896.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+11061_67+11072d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887449 | ||||||
| chrX:150887449
|
GAAAT | G | 1 | a0001c0001t0009g0180 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.67+11069_67+11072d others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887449 | ||||||
| chrX:150887449
|
GAAATAAA others(1): Show |
G | 2 | a0001c0001t0001g0115a0001c0001t0005g0141 | 2 | HG01884.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.67+11065_67+11072d others(10): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887449 | ||||||
| chrX:150887449
|
GAAATAAA others(5): Show |
G | 1 | a0001c0001t0001g0024 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.67+11061_67+11072d others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887449 | ||||||
| chrX:150887658
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.67+10864G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887658 | ||||||
| chrX:150887749
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+10773C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887749 | ||||||
| chrX:150887803
|
GA | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+10718delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887803 | ||||||
| chrX:150888006
|
G | GTGCGGCA others(15): Show |
21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(18): Show | 21 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+10494_67+10515d others(24): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150888006 | ||||||
| chrX:150888298
|
G | C | 7 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+10224C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150888298 | ||||||
| chrX:150888410
|
TA | T | 1 | a0001c0001t0001g0048 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.67+10111delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150888410 | ||||||
| chrX:150888477
|
T | C | 3 | a0001c0001t0011g0163a0001c0001t0011g0164a0001c0001t0025g0144 | 3 | HG01884.hp2 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.67+10045A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150888477 | ||||||
| chrX:150888489
|
G | A | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+10033C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150888489 | ||||||
| chrX:150888525
|
G | GA | 1 | a0001c0001t0002g0087 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.67+9996dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150888525 | ||||||
| chrX:150888817
|
T | TA | 1 | a0001c0001t0013g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.67+9704dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150888817 | ||||||
| chrX:150888910
|
C | T | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+9612G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150888910 | ||||||
| chrX:150889088
|
T | G | 7 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+9434A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889088 | ||||||
| chrX:150889114
|
T | C | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+9408A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889114 | ||||||
| chrX:150889208
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+9314C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889208 | ||||||
| chrX:150889399
|
C | T | 3 | a0001c0001t0002g0067a0001c0001t0007g0204a0001c0001t0031g0158 | 3 | HG02280.hp2 HG03239.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.67+9123G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889399 | ||||||
| chrX:150889467
|
T | TA | 1 | a0001c0001t0002g0042 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.67+9054dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889467 | ||||||
| chrX:150889467
|
T | TAA | 14 | a0001c0001t0001g0115a0001c0001t0005g0202a0001c0001t0005g0203others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+9053_67+9054dup others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889467 | ||||||
| chrX:150889471
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0039g0170 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.67+9051T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889471 | ||||||
| chrX:150889476
|
A | AAC | 1 | a0001c0001t0008g0161 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.67+9045_67+9046ins others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889476 | ||||||
| chrX:150889508
|
G | A | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198 | 3 | HG02145.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.67+9014C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889508 | ||||||
| chrX:150889526
|
T | C | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+8996A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889526 | ||||||
| chrX:150889686
|
A | G | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.67+8836T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889686 | ||||||
| chrX:150889763
|
CCG | C | 1 | a0001c0002t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.67+8757_67+8758del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889763 | ||||||
| chrX:150889959
|
T | C | 52 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.67+8563A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150889959 | ||||||
| chrX:150890014
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+8508C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890014 | ||||||
| chrX:150890018
|
A | T | 70 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.67+8504T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890018 | ||||||
| chrX:150890085
|
G | A | 7 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0008g0161others(4): Show | 7 | HG02258.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+8437C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890085 | ||||||
| chrX:150890127
|
T | G | 9 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0005g0202others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+8395A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890127 | ||||||
| chrX:150890151
|
A | AAAAT | 1 | a0001c0001t0004g0047 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67+8367_67+8370dup others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890151 | ||||||
| chrX:150890151
|
A | AAAATAAA others(5): Show |
2 | a0001c0001t0008g0161a0001c0001t0019g0174 | 2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.67+8359_67+8370dup others(12): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890151 | ||||||
| chrX:150890151
|
A | AAAATAAA others(9): Show |
6 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0005g0202others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+8355_67+8370dup others(16): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890151 | ||||||
| chrX:150890151
|
AAAATAAA others(1): Show |
A | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.67+8363_67+8370del others(8): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890151 | ||||||
| chrX:150890300
|
G | GA | 1 | a0001c0002t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.67+8221dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890300 | ||||||
| chrX:150890307
|
C | T | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+8215G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890307 | ||||||
| chrX:150890348
|
A | G | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+8174T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890348 | ||||||
| chrX:150890352
|
G | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+8170C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890352 | ||||||
| chrX:150890827
|
T | TG | 1 | a0001c0002t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.67+7694dupC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890827 | ||||||
| chrX:150890913
|
C | A | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+7609G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890913 | ||||||
| chrX:150890950
|
C | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+7572G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150890950 | ||||||
| chrX:150891111
|
T | G | 1 | a0001c0001t0024g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67+7411A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891111 | ||||||
| chrX:150891189
|
C | T | 7 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+7333G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891189 | ||||||
| chrX:150891376
|
A | G | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.67+7146T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891376 | ||||||
| chrX:150891394
|
T | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.67+7128A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891394 | ||||||
| chrX:150891542
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.67+6980C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891542 | ||||||
| chrX:150891565
|
A | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.67+6957T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891565 | ||||||
| chrX:150891573
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.67+6949C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891573 | ||||||
| chrX:150891767
|
C | A | 15 | a0001c0001t0001g0115a0001c0001t0005g0202a0001c0001t0005g0203others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+6755G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891767 | ||||||
| chrX:150891810
|
A | AG | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.67+6711_67+6712ins others(1): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891810 | ||||||
| chrX:150891844
|
TG | T | 1 | a0001c0001t0001g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.67+6677delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150891844 | ||||||
| chrX:150892335
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.67+6187C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892335 | ||||||
| chrX:150892381
|
CG | C | 1 | a0001c0001t0035g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.67+6140delC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892381 | ||||||
| chrX:150892605
|
C | CA | 16 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0043others(13): Show | 16 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+5916dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892605 | ||||||
| chrX:150892605
|
C | CAA | 1 | a0001c0001t0003g0103 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.67+5915_67+5916dup others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892605 | ||||||
| chrX:150892605
|
CA | C | 61 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0069others(58): Show | 61 | HG00140.hp1 HG01070.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.67+5916delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892605 | ||||||
| chrX:150892605
|
CAA | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.67+5915_67+5916del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892605 | ||||||
| chrX:150892605
|
CAAA | C | 2 | a0001c0001t0001g0134a0001c0001t0005g0133 | 2 | HG00323.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.67+5914_67+5916del others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892605 | ||||||
| chrX:150892605
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+5903_67+5916del others(14): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892605 | ||||||
| chrX:150892632
|
G | A | 4 | a0001c0001t0004g0035a0001c0001t0004g0064a0001c0001t0004g0199others(1): Show | 4 | HG00323.hp1 HG01167.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5890C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892632 | ||||||
| chrX:150892641
|
A | G | 13 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0192others(10): Show | 13 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.67+5881T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892641 | ||||||
| chrX:150892652
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0157 | 3 | NA18966.hp1 NA19058.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.67+5870G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892652 | ||||||
| chrX:150892726
|
C | T | 29 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0134others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.67+5796G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892726 | ||||||
| chrX:150892814
|
T | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.67+5708A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892814 | ||||||
| chrX:150892938
|
A | G | 12 | a0001c0001t0001g0115a0001c0001t0007g0196a0001c0001t0007g0197others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+5584T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892938 | ||||||
| chrX:150893071
|
A | T | 12 | a0001c0001t0001g0115a0001c0001t0007g0196a0001c0001t0007g0197others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+5451T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150893071 | ||||||
| chrX:150893169
|
C | T | 2 | a0001c0001t0021g0117a0001c0001t0021g0150 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.67+5353G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150893169 | ||||||
| chrX:150893239
|
TTC | T | 4 | a0001c0001t0002g0140a0001c0001t0008g0139a0001c0001t0016g0072others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5281_67+5282del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150893239 | ||||||
| chrX:150893282
|
A | G | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.67+5240T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150893282 | ||||||
| chrX:150893515
|
G | GC | 1 | a0001c0001t0001g0065 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.67+5006dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150893515 | ||||||
| chrX:150893648
|
AC | A | 1 | a0001c0002t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.67+4873delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150893648 | ||||||
| chrX:150893835
|
C | T | 2 | a0001c0001t0001g0110a0003c0004t0042g0209 | 2 | HG00099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.67+4687G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150893835 | ||||||
| chrX:150893859
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67+4663C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150893859 | ||||||
| chrX:150894007
|
C | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(18): Show | 21 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+4515G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150894007 | ||||||
| chrX:150894458
|
C | A | 4 | a0001c0001t0008g0161a0001c0001t0008g0168a0001c0001t0019g0174others(1): Show | 4 | HG02451.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+4064G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150894458 | ||||||
| chrX:150894571
|
T | TTGTG | 4 | a0001c0001t0001g0193a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+3947_67+3950dup others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150894571 | ||||||
| chrX:150894571
|
TTG | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 142 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.67+3949_67+3950del others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150894571 | ||||||
| chrX:150894571
|
TTGTG | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.67+3947_67+3950del others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150894571 | ||||||
| chrX:150894571
|
TTGTGTG | T | 13 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0007g0196others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+3945_67+3950del others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150894571 | ||||||
| chrX:150894641
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+3881C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150894641 | ||||||
| chrX:150894880
|
C | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(18): Show | 21 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+3642G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150894880 | ||||||
| chrX:150895051
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0002g0016 | 2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.67+3471A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150895051 | ||||||
| chrX:150895154
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.67+3368G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150895154 | ||||||
| chrX:150895155
|
G | A | 3 | a0001c0001t0006g0191a0001c0001t0009g0189a0001c0001t0024g0190 | 3 | HG02257.hp2 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.67+3367C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150895155 | ||||||
| chrX:150895161
|
A | G | 1 | a0001c0001t0011g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67+3361T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150895161 | ||||||
| chrX:150895183
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0018g0104a0001c0001t0018g0105 | 3 | NA18945.hp1 NA18960.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.67+3339C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150895183 | ||||||
| chrX:150895478
|
T | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0005g0202others(13): Show | 16 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+3044A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150895478 | ||||||
| chrX:150895975
|
G | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(18): Show | 21 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+2547C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150895975 | ||||||
| chrX:150895982
|
C | T | 1 | a0001c0001t0008g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67+2540G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150895982 | ||||||
| chrX:150896026
|
C | CA | 4 | a0001c0001t0001g0106a0001c0001t0003g0131a0001c0001t0039g0170others(1): Show | 4 | HG00621.hp1 HG02135.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2495dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896026 | ||||||
| chrX:150896026
|
C | CAA | 12 | a0001c0001t0001g0115a0001c0001t0007g0196a0001c0001t0007g0197others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+2494_67+2495dup others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896026 | ||||||
| chrX:150896026
|
C | CAAA | 3 | a0001c0001t0001g0193a0001c0001t0005g0202a0001c0001t0005g0203 | 3 | HG02109.hp1 HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.67+2493_67+2495dup others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896026 | ||||||
| chrX:150896026
|
C | CAAAA | 1 | a0001c0002t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.67+2492_67+2495dup others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896026 | ||||||
| chrX:150896026
|
CA | C | 3 | a0001c0001t0001g0109a0001c0001t0002g0027a0001c0001t0002g0076 | 3 | HG01943.hp1 NA19070.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.67+2495delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896026 | ||||||
| chrX:150896074
|
A | C | 13 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0192others(10): Show | 13 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.67+2448T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896074 | ||||||
| chrX:150896237
|
A | T | 1 | a0001c0001t0001g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.67+2285T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896237 | ||||||
| chrX:150896359
|
C | T | 13 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0005g0202others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+2163G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896359 | ||||||
| chrX:150896363
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01070.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.67+2159T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896363 | ||||||
| chrX:150896410
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67+2112A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896410 | ||||||
| chrX:150896413
|
T | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(19): Show | 22 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+2109A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896413 | ||||||
| chrX:150896735
|
A | G | 40 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(37): Show | 40 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.67+1787T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896735 | ||||||
| chrX:150896796
|
C | T | 1 | a0002c0003t0012g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.67+1726G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896796 | ||||||
| chrX:150896970
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+1552T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896970 | ||||||
| chrX:150897215
|
CCTTT | C | 1 | a0001c0001t0001g0192 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67+1303_67+1306del others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897215 | ||||||
| chrX:150897314
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+1208T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897314 | ||||||
| chrX:150897526
|
A | AGT | 47 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0109others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.67+994_67+995dupAC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897526 | ||||||
| chrX:150897526
|
A | AGTGT | 4 | a0001c0001t0001g0205a0001c0001t0005g0202a0001c0001t0005g0203others(1): Show | 4 | HG01099.hp1 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+992_67+995dupAC others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897526 | ||||||
| chrX:150897526
|
A | AGTGTGT | 6 | a0001c0001t0001g0193a0001c0001t0007g0196a0001c0001t0007g0197others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+990_67+995dupAC others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897526 | ||||||
| chrX:150897526
|
A | AGTGTGTG others(1): Show |
2 | a0001c0001t0007g0204a0001c0002t0001g0201 | 2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.67+988_67+995dupAC others(6): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897526 | ||||||
| chrX:150897526
|
AGT | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(12): Show | 15 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+994_67+995delAC | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897526 | ||||||
| chrX:150897526
|
AGTGT | A | 1 | a0001c0001t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+992_67+995delAC others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897526 | ||||||
| chrX:150897604
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.67+918T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897604 | ||||||
| chrX:150897863
|
C | A | 2 | a0001c0001t0043g0211a0001c0001t0044g0210 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.67+659G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897863 | ||||||
| chrX:150897875
|
T | A | 1 | a0001c0001t0001g0018 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.67+647A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897875 | ||||||
| chrX:150897958
|
C | A | 1 | a0001c0001t0043g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+564G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150897958 | ||||||
| chrX:150898054
|
A | AAC | 2 | a0001c0001t0001g0108a0001c0001t0002g0107 | 2 | HG01258.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.67+467_67+468insGT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
A | AACC | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0068 | 3 | HG01261.hp1 HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.67+467_67+468insGG others(1): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
A | AC | 39 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0077others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.67+467dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
A | ACC | 34 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043others(31): Show | 34 | HG00741.hp2 HG01081.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.67+466_67+467dupGG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
A | ACCC | 12 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(9): Show | 12 | HG00609.hp1 HG01167.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+465_67+467dupGG others(1): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
A | ACCCC | 5 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG00735.hp1 HG02040.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+464_67+467dupGG others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
A | ACCCCCCC | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.67+461_67+467dupGG others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
AC | A | 26 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0153others(23): Show | 26 | HG00323.hp2 HG01255.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.67+467delG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
ACC | A | 10 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0008g0161others(7): Show | 10 | HG01884.hp2 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+466_67+467delGG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
ACCC | A | 15 | a0001c0001t0001g0193a0001c0001t0005g0169a0001c0001t0005g0202others(12): Show | 15 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.67+465_67+467delGG others(1): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
ACCCC | A | 3 | a0001c0001t0014g0172a0001c0001t0019g0174a0001c0002t0001g0173 | 3 | HG02257.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.67+464_67+467delGG others(2): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
ACCCCC | A | 4 | a0001c0001t0001g0175a0001c0001t0004g0176a0001c0001t0010g0177others(1): Show | 4 | HG02738.hp1 HG03486.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+463_67+467delGG others(3): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
ACCCCCC | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(28): Show | 31 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.67+462_67+467delGG others(4): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898054
|
ACCCCCCC | A | 1 | a0001c0001t0007g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+461_67+467delGG others(5): Show |
CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | ||||||
| chrX:150898061
|
C | G | 8 | a0001c0001t0001g0193a0001c0001t0007g0196a0001c0001t0007g0197others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+461G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898061 | ||||||
| chrX:150898064
|
C | G | 1 | a0001c0001t0017g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+458G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898064 | ||||||
| chrX:150898067
|
C | A | 8 | a0001c0001t0001g0193a0001c0001t0007g0196a0001c0001t0007g0197others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+455G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898067 | ||||||
| chrX:150898067
|
C | G | 1 | a0001c0001t0010g0019 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.67+455G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898067 | ||||||
| chrX:150898069
|
C | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0014others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+453G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898069 | ||||||
| chrX:150898085
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004 | 3 | HG00735.hp1 HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.67+437G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898085 | ||||||
| chrX:150898097
|
G | A | 1 | a0001c0001t0004g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.67+425C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898097 | ||||||
| chrX:150898152
|
T | C | 1 | a0001c0001t0005g0200 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67+370A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898152 | ||||||
| chrX:150898199
|
T | C | 3 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0002t0001g0201 | 3 | HG02258.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67+323A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898199 | ||||||
| chrX:150898236
|
T | C | 1 | a0001c0001t0007g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+286A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898236 | ||||||
| chrX:150898302
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.67+220C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898302 | ||||||
| chrX:150898504
|
G | GC | 2 | a0001c0001t0001g0206a0001c0001t0012g0207 | 2 | HG03139.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.67+17dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898504 |