Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MVAWR others(257): Show |
chrX | 150761336 | 150903668 |
| a0002 | 0/0 | 262 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | MVAWR others(257): Show |
chrX | 150761336 | 150903668 |
| a0003 | 0/0 | 262 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | MVAWR others(257): Show |
chrX | 150761336 | 150903668 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 786 | 201 | 56 | 34 | 74 | 13 | 22 | CD99L2_chrX_150761336_150903668 | CD99L2 | ATGGT others(781): Show |
chrX | 150761336 | 150903668 | ||
| a0001c0002 | 0/0 | 786 | 8 | 4 | 0 | 4 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | ATGGT others(781): Show |
chrX | 150761336 | 150903668 | ||
| a0001c0004 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | ATGGT others(781): Show |
chrX | 150761336 | 150903668 | ||
| a0002c0005 | 0/0 | 786 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | ATGGT others(781): Show |
chrX | 150761336 | 150903668 | ||
| a0003c0003 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | ATGGT others(781): Show |
chrX | 150761336 | 150903668 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3567 | 88 | 8 | 15 | 54 | 4 | 6 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0002 | 0/0 | 3567 | 20 | 2 | 10 | 4 | 2 | 2 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0003 | 0/0 | 3567 | 11 | 0 | 0 | 6 | 0 | 5 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0004 | 0/1 | 3567 | 10 | 1 | 2 | 4 | 0 | 2 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0005 | 0/0 | 3567 | 6 | 5 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0006 | 0/0 | 3567 | 5 | 1 | 1 | 0 | 2 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0007 | 0/0 | 3567 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0008 | 0/0 | 3570 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3565): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0009 | 0/0 | 3567 | 4 | 4 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0010 | 0/0 | 3567 | 4 | 0 | 2 | 0 | 1 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0011 | 0/0 | 3567 | 3 | 3 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0012 | 0/0 | 3567 | 2 | 2 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0013 | 0/0 | 3567 | 3 | 0 | 0 | 0 | 0 | 3 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0014 | 0/0 | 3570 | 3 | 3 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3565): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0015 | 0/0 | 3567 | 2 | 0 | 1 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0016 | 0/0 | 3567 | 2 | 2 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0017 | 0/0 | 3570 | 2 | 2 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3565): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0018 | 0/0 | 3567 | 2 | 0 | 0 | 2 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0019 | 0/0 | 3567 | 2 | 1 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0020 | 0/0 | 3567 | 2 | 0 | 0 | 2 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0021 | 0/0 | 3567 | 2 | 0 | 0 | 0 | 2 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0023 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0024 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3565): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0025 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0026 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0027 | 0/0 | 3567 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0028 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0029 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0030 | 0/0 | 3567 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0031 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0032 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0033 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0034 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3565): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0035 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0036 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0037 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0038 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0039 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0040 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0042 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0001t0043 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3565): Show |
chrX | 150761336 | 150903668 |
| a0001c0002t0001 | 0/0 | 3567 | 6 | 3 | 0 | 3 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0002t0002 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0002t0022 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0001c0004t0001 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0002c0005t0041 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
chrX | 150761336 | 150903668 |
| a0003c0003t0012 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | CTCCC others(3562): Show |
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 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0016 | 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 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0028 | 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 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0038 | 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 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0045 | 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 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0052 | 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 |
| a0001c0001t0001g0054 | 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 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0090 | 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 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0177 | 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 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0006g0194 | 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 |
| a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0009g0197 | 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 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0013g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0013g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0014g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0014g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0014g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0015g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0015g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0016g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0016g0069 | 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 |
| a0001c0001t0017g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0018g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0018g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0019g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0019g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0020g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0020g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0021g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0021g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0023g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0025g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0026g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0027g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0028g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0029g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0030g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0031g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0032g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0033g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0034g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0035g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0036g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0037g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0038g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0039g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0040g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0042g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0001t0043g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0002t0022g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0002c0005t0041g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| a0003c0003t0012g0148 | 0/0 | 1 | 1 | 0 | 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 | g0188 | EUR | GBR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0078 | EUR | GBR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00323 | hp1 | a0001 | c0001 | t0015 | g0146 | EUR | FIN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00438 | hp2 | a0001 | c0001 | t0040 | g0208 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00673 | hp1 | a0001 | c0002 | t0022 | g0097 | EAS | CHS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0110 | 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 | g0037 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0039 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0180 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0030 | 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 | a0002 | c0005 | t0041 | g0209 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01243 | hp1 | a0001 | c0001 | t0043 | g0210 | AMR | PUR | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0155 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01496 | hp2 | a0001 | c0001 | t0015 | g0151 | AMR | CLM | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01515 | hp1 | a0001 | c0001 | t0021 | g0127 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01516 | hp2 | a0001 | c0001 | t0027 | g0169 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0154 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01517 | hp2 | a0001 | c0001 | t0021 | g0168 | EUR | IBS | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0124 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01934 | hp1 | a0001 | c0001 | t0034 | g0149 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | KHV | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0200 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0105 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02257 | hp2 | a0001 | c0001 | t0024 | g0193 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02280 | hp1 | a0001 | c0001 | t0036 | g0161 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0176 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0125 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02615 | hp2 | a0003 | c0003 | t0012 | g0148 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02630 | hp1 | a0001 | c0001 | t0028 | g0070 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0196 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0192 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0157 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0111 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02886 | hp1 | a0001 | c0001 | t0025 | g0162 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0131 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02895 | hp1 | a0001 | c0001 | t0023 | g0006 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0069 | 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 | g0187 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03041 | hp1 | a0001 | c0001 | t0026 | g0167 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0160 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03098 | hp1 | a0001 | c0001 | t0038 | g0178 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0186 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03209 | hp1 | a0001 | c0001 | t0035 | g0163 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03225 | hp1 | a0001 | c0001 | t0029 | g0126 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0041 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0197 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0118 | AFR | ESN | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03540 | hp1 | a0001 | c0001 | t0031 | g0114 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0165 | AFR | GWD | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0068 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03654 | hp1 | a0001 | c0001 | t0030 | g0040 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0033 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0201 | SAS | BEB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03942 | hp1 | a0001 | c0001 | t0019 | g0115 | SAS | BEB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG04115 | hp1 | a0001 | c0001 | t0013 | g0073 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | STU | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0120 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0179 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18906 | hp2 | a0001 | c0001 | t0033 | g0166 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18945 | hp1 | a0001 | c0001 | t0018 | g0101 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18960 | hp1 | a0001 | c0001 | t0018 | g0102 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0089 | 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 | g0049 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18979 | hp1 | a0001 | c0001 | t0020 | g0057 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19000 | hp1 | a0001 | c0001 | t0020 | g0145 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0199 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19043 | hp1 | a0001 | c0001 | t0019 | g0122 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19075 | hp1 | a0001 | c0001 | t0039 | g0007 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19240 | hp1 | a0001 | c0001 | t0042 | g0211 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0181 | AFR | YRI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20129 | hp1 | a0001 | c0001 | t0032 | g0183 | AFR | ASW | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0121 | 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 | g0091 | EUR | TSI | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20905 | hp1 | a0001 | c0001 | t0013 | g0067 | SAS | GIH | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02559 | hp1 | a0001 | c0001 | t0037 | g0152 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0117 | AFR | ACB | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | MSL | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | USA | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | USA | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0164 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0084 | REF | REF | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0147 | REF | REF | CD99L2_chrX_150761336_150903668 | CD99L2 | chrX | 150761336 | 150903668 |
| view | 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 | a0002 | 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 | a0002 | 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 | a0002 | 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:150777449 | C | T | 1 | a0003 | 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 |
| view | 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 | a0001c0002 a0001c0004 |
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 | a0001c0004 | 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 |
| view | 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:150766592 | A | AGTT | 6 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0017 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
81 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(78): 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: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 | a0001c0001t0011 a0001c0001t0026 |
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 | a0001c0001t0038 | 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 | a0001c0001t0035 | 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:150767630 | C | A | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(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:150768198 | G | A | 1 | a0001c0001t0034 | 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 | a0001c0001t0014 a0001c0001t0028 a0001c0001t0032 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(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 | a0001c0001t0007 a0001c0001t0042 |
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 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0021 others(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 | a0001c0001t0012 a0001c0001t0028 a0001c0001t0029 others(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 | a0001c0001t0011 a0001c0001t0024 a0001c0001t0025 others(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: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 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(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:150768959 | T | C | 1 | a0001c0001t0039 | 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:150898619 | G | C | 1 | a0001c0001t0040 | 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 | a0002c0005t0041 | 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 | a0001c0001t0042 a0001c0001t0043 |
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 |
| view | 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 | a0001c0001t0001g0156 a0001c0001t0002g0110 |
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 | 24 | a0001c0001t0001g0075 a0001c0001t0001g0109 a0001c0001t0001g0195 others(21): Show |
24 | HG00140.hp1 HG00280.hp1 HG01081.hp2 others(21): 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 | a0001c0001t0014g0105 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0010g0180 | 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 | a0001c0001t0015g0146 | 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 | a0001c0001t0009g0197 | 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 | a0001c0001t0017g0020 a0001c0001t0017g0196 a0001c0002t0001g0121 |
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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0123 a0001c0001t0002g0005 a0001c0001t0004g0108 others(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 | a0001c0001t0017g0020 a0001c0001t0017g0196 a0001c0002t0001g0121 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0106 others(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:150769761 | T | C | 50 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0002t0001g0010 a0001c0002t0022g0097 |
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:150770006 | G | A | 1 | a0001c0001t0001g0116 | 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 | a0001c0001t0002g0158 a0001c0001t0008g0157 a0001c0001t0017g0196 |
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 | a0001c0001t0004g0201 | 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 | a0001c0001t0013g0073 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0007g0198 others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0055 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0080 a0001c0001t0001g0133 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0028g0070 | 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 | a0001c0001t0008g0120 | 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 | a0001c0001t0008g0120 | 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 | a0001c0001t0005g0159 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | 48 | a0001c0001t0001g0065 a0001c0001t0001g0072 a0001c0001t0001g0079 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): 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 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.656-786C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150771155 | |||||||
| chrX:150771224 | G | A | 1 | a0001c0001t0006g0194 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0048 |
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 | a0001c0001t0035g0163 | 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 | a0001c0001t0007g0206 a0001c0001t0033g0166 |
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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0001t0009g0197 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0027g0169 | 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 | a0001c0001t0027g0169 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0023g0006 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0007g0198 others(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 | a0001c0001t0005g0159 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.656-2196G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150772565 | |||||||
| chrX:150773251 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0002t0001g0203 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0133 a0001c0001t0001g0187 others(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 | a0001c0001t0016g0068 a0001c0001t0016g0069 a0001c0001t0017g0020 |
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 | a0001c0001t0005g0159 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0005g0159 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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: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:150774327 | G | A | 3 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0002g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.655+1801C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774373 | |||||||
| chrX:150774410 | C | T | 10 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0052 others(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 | 38 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0107 others(35): Show |
38 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(35): 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 | a0001c0001t0001g0036 a0001c0002t0001g0010 a0001c0002t0022g0097 |
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:150774714 | C | T | 3 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0001g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.655+1442G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150774732 | |||||||
| chrX:150775342 | C | T | 1 | a0001c0001t0001g0129 | 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 | a0001c0001t0004g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.655+783C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775391 | |||||||
| chrX:150775571 | G | T | 1 | a0001c0001t0043g0210 | 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 | 62 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0054 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.655+523C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775651 | |||||||
| chrX:150775852 | G | T | 1 | a0001c0001t0033g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.655+322C>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 9/10 | chrX | 150775852 | |||||||
| chrX:150775861 | A | G | 1 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0150 a0001c0001t0002g0023 a0001c0001t0002g0081 others(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 | a0001c0001t0004g0108 a0001c0001t0026g0167 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
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 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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:150776368 | T | C | 1 | a0001c0001t0001g0044 | 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 | a0001c0001t0039g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.536-117G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776410 | |||||||
| chrX:150776719 | C | G | 12 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0065 others(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:150776963 | G | C | 1 | a0002c0005t0041g0209 | 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 | a0002c0005t0041g0209 | 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 | a0002c0005t0041g0209 | 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 | a0001c0001t0008g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.535+468T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 8/10 | chrX | 150776976 | |||||||
| chrX:150777242 | G | A | 2 | a0001c0001t0004g0108 a0001c0001t0026g0167 |
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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0150 a0001c0001t0002g0023 a0001c0001t0002g0081 others(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 | a0001c0001t0004g0062 a0001c0001t0006g0039 |
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 | a0001c0002t0001g0203 a0003c0003t0012g0148 |
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 | a0001c0001t0001g0016 | 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 | a0001c0001t0004g0135 | 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 | a0001c0001t0006g0078 | 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 | a0001c0001t0001g0123 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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:150778508 | G | A | 2 | a0001c0001t0016g0068 a0001c0001t0016g0069 |
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:150778576 | A | G | 11 | a0001c0001t0001g0072 a0001c0001t0001g0119 a0001c0001t0005g0159 others(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 | TA | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0007g0198 others(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 | TAAA | T | 10 | a0001c0001t0001g0090 a0001c0001t0001g0119 a0001c0001t0001g0123 others(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:150778683 | A | T | 6 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0008g0176 others(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 | AAAATAT | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0065 others(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 | AAATATAT | A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0088 others(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 | T | 14 | a0001c0001t0001g0072 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0003g0083 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0106 others(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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): 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 | ATAT | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0116 others(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 | a0001c0001t0013g0033 a0001c0001t0013g0067 a0001c0001t0023g0006 |
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 | a0001c0001t0025g0162 a0001c0001t0035g0163 a0001c0001t0036g0161 |
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 | a0001c0001t0003g0083 | 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 | a0001c0001t0001g0016 a0001c0002t0002g0011 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0144 a0001c0001t0001g0150 others(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 | a0001c0001t0004g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.497-1223A>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778705 | |||||||
| chrX:150778875 | A | G | 1 | a0001c0001t0004g0062 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.497-1393T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150778875 | |||||||
| chrX:150779081 | C | A | 2 | a0001c0002t0001g0182 a0001c0004t0001g0131 |
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:150779383 | TC | T | 3 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0019g0122 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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:150780010 | G | A | 1 | a0001c0001t0042g0211 | 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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0002t0002g0011 | 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 | a0001c0001t0042g0211 | 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 | a0001c0001t0042g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.497-3067A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150780549 | |||||||
| chrX:150780905 | G | A | 1 | a0001c0001t0042g0211 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 |
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 | a0001c0001t0008g0160 | 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 | a0001c0001t0003g0096 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0195 a0001c0001t0008g0120 |
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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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:150782557 | C | T | 2 | a0001c0002t0001g0182 a0001c0004t0001g0131 |
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 | a0001c0001t0010g0111 | 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 | a0001c0001t0009g0181 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0119 a0001c0001t0008g0120 |
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 | a0001c0001t0005g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.497-5533A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150783015 | |||||||
| chrX:150783240 | G | A | 2 | a0001c0001t0001g0016 a0001c0002t0002g0011 |
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 | a0001c0001t0002g0023 a0001c0001t0002g0081 a0001c0001t0002g0128 |
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:150783301 | C | A | 3 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0074 |
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:150784115 | G | T | 1 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0003g0174 | 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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
120 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.497-6781G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150784263 | |||||||
| chrX:150784425 | A | G | 3 | a0001c0001t0007g0206 a0001c0001t0017g0020 a0001c0001t0017g0196 |
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 | a0001c0001t0001g0133 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150786139 | T | A | 1 | a0001c0002t0002g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.496+7552A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150786139 | |||||||
| chrX:150786225 | T | G | 47 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0119 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0001g0184 others(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 | a0001c0001t0042g0211 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0123 a0001c0001t0014g0105 a0001c0001t0014g0117 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0001g0036 a0001c0002t0001g0010 |
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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0156 a0001c0001t0002g0158 others(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 | a0001c0001t0001g0087 a0001c0001t0002g0049 a0002c0005t0041g0209 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0002g0110 others(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 | a0001c0001t0015g0151 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(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 | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(53): Show |
57 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(54): 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 | a0001c0001t0001g0072 a0001c0001t0017g0020 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0036 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0009g0165 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0001g0133 others(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:150788109 | T | C | 91 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.496+5316G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150788375 | |||||||
| chrX:150788704 | C | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.496+4987G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150788704 | |||||||
| chrX:150788779 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
119 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(116): 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0035g0163 | 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 | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.496+4566delA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789124 | |||||||
| chrX:150789124 | CTT | C | 7 | a0001c0001t0001g0015 a0001c0001t0008g0176 a0001c0001t0014g0105 others(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:150789192 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.496+4499T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789192 | |||||||
| chrX:150789225 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): 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 | a0001c0001t0001g0099 | 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
122 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.496+4144T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789547 | |||||||
| chrX:150789658 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.496+4033T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150789658 | |||||||
| chrX:150789994 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0159 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0023g0006 | 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 | a0001c0001t0009g0181 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0055 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0001g0032 | 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 | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.496+1774C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150791917 | |||||||
| chrX:150792008 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
119 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(116): 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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0207 |
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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0007g0206 a0001c0001t0017g0020 a0001c0001t0017g0196 |
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 | a0001c0001t0001g0104 | 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 | a0001c0001t0023g0006 | 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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): 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 | a0001c0001t0023g0006 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.496+380C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 7/10 | chrX | 150793311 | |||||||
| chrX:150793849 | TCCCAGTT others(13): Show |
T | 1 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0170 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.431-136A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 6/10 | chrX | 150793892 | |||||||
| chrX:150793928 | G | A | 2 | a0001c0001t0042g0211 a0001c0001t0043g0210 |
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 | a0001c0001t0001g0025 | 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 | a0001c0001t0026g0167 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0015g0151 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0002g0077 a0001c0001t0006g0041 |
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 | a0001c0001t0001g0053 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0023g0006 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0017g0196 | 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 | a0001c0001t0002g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-45A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 5/10 | chrX | 150795334 | |||||||
| chrX:150795665 | G | T | 1 | a0001c0001t0003g0082 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150796270 | T | C | 16 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0028g0070 a0001c0001t0036g0161 |
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:150796429 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150796904 | G | A | 1 | a0001c0001t0004g0135 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0187 others(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 | a0001c0001t0004g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.278-1686T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797172 | |||||||
| chrX:150797221 | T | C | 18 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0187 others(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 | a0001c0002t0001g0010 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.278-2026G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797512 | |||||||
| chrX:150797732 | C | G | 1 | a0001c0001t0003g0112 | 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 | a0001c0001t0001g0058 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.278-2297C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150797783 | |||||||
| chrX:150797883 | A | C | 1 | a0001c0001t0005g0205 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0032 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.278-2542A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798028 | |||||||
| chrX:150798046 | AAAG | A | 6 | a0001c0001t0001g0187 a0001c0001t0002g0158 a0001c0001t0008g0157 others(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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.278-2619G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798105 | |||||||
| chrX:150798107 | C | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): 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 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0001t0004g0108 others(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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0028g0070 a0001c0001t0036g0161 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0189 |
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:150798162 | GGAAA | G | 3 | a0001c0001t0002g0023 a0001c0001t0002g0081 a0001c0001t0002g0128 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150798166 | A | G | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0002g0023 a0001c0001t0002g0081 a0001c0001t0002g0128 |
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 | a0001c0001t0002g0023 a0001c0001t0002g0081 a0001c0001t0002g0128 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0075 a0001c0001t0001g0150 |
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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
98 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(95): 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:150798185 | G | A | 51 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | GGGAGGAA others(1): Show |
G | 11 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0071 others(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 | a0001c0001t0035g0163 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0001t0001g0106 others(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:150798209 | A | G | 15 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0071 others(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 | a0001c0001t0042g0211 | 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 | a0001c0001t0035g0163 | 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 | a0001c0001t0042g0211 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0042g0211 | 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 | a0001c0001t0042g0211 | 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(13): Show |
1 | a0001c0001t0008g0157 | 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 | a0001c0001t0003g0174 a0001c0001t0039g0007 |
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 | a0001c0001t0005g0159 a0001c0001t0034g0149 |
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 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0001t0001g0106 others(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:150798234 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): 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 | a0001c0001t0001g0113 | 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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): 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 | a0001c0001t0001g0113 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): 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 | a0001c0001t0001g0113 | 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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.278-2760T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798246 | |||||||
| chrX:150798313 | G | C | 1 | a0001c0001t0004g0047 | 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 | a0001c0001t0005g0204 | 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 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.278-2944C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150798430 | |||||||
| chrX:150798910 | C | T | 18 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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:150799135 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.278-3649A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799135 | |||||||
| chrX:150799335 | CA | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150799480 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.278-3994G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799480 | |||||||
| chrX:150799513 | CA | C | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-4042C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150799528 | |||||||
| chrX:150799742 | G | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150799887 | T | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150800701 | G | T | 1 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0139 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.278-5315C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150800801 | |||||||
| chrX:150800883 | A | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150801026 | C | T | 1 | a0001c0001t0033g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.278-5540G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150801026 | |||||||
| chrX:150801043 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0002g0110 |
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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0140 | 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 | a0001c0001t0011g0124 a0001c0001t0011g0125 a0001c0001t0011g0179 others(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 | a0001c0001t0001g0009 a0001c0001t0036g0161 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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:150801676 | C | T | 1 | a0001c0001t0001g0100 | 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 | a0001c0001t0021g0127 a0001c0001t0021g0168 |
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:150801894 | G | A | 1 | a0001c0001t0007g0198 | 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 | a0001c0001t0004g0030 a0001c0001t0015g0146 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | AT | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0159 | 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 | a0001c0001t0042g0211 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0172 | 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 | 11 | a0001c0001t0001g0024 a0001c0001t0001g0058 a0001c0001t0001g0106 others(8): Show |
11 | HG01256.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-7395dupA | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150802880 | |||||||
| chrX:150802880 | C | CTT | 7 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0026 others(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 | a0001c0001t0004g0030 a0001c0001t0008g0120 a0001c0001t0015g0146 others(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 | CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0001g0187 a0001c0001t0004g0108 a0001c0001t0009g0192 others(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 | a0001c0001t0001g0036 a0001c0001t0003g0095 a0001c0001t0003g0141 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0002g0014 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(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 | a0001c0001t0042g0211 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0014 |
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 | a0001c0001t0001g0119 | 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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0004g0089 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0142 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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:150804564 | C | T | 3 | a0001c0001t0011g0124 a0001c0001t0011g0125 a0001c0001t0011g0179 |
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 | a0001c0001t0003g0112 | 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 | a0001c0001t0007g0200 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0008g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.278-9659C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805145 | |||||||
| chrX:150805270 | C | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | a0001c0001t0014g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.277+9577A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805285 | |||||||
| chrX:150805618 | T | C | 5 | a0001c0001t0001g0119 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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:150805739 | G | C | 1 | a0001c0001t0003g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.277+9123C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805739 | |||||||
| chrX:150805778 | G | A | 50 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150805988 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.277+8874T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150805988 | |||||||
| chrX:150806312 | G | C | 2 | a0001c0001t0004g0062 a0001c0001t0004g0201 |
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:150806706 | C | A | 1 | a0001c0001t0001g0050 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.277+8156G>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806706 | |||||||
| chrX:150806773 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.277+8089G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150806773 | |||||||
| chrX:150807123 | G | A | 11 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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:150807158 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
135 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.277+7704G>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 4/10 | chrX | 150807158 | |||||||
| chrX:150807462 | A | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0123 others(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:150807743 | CTG | C | 4 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0060 a0001c0001t0003g0095 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0060 a0001c0001t0003g0095 others(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 | a0001c0001t0007g0206 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0014g0105 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
114 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(111): 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 | a0001c0001t0001g0106 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0195 | 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 | a0001c0002t0002g0011 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150814528 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0172 a0001c0001t0001g0207 |
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:150814652 | G | A | 16 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0042g0211 a0001c0001t0043g0210 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0002t0001g0203 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
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 | a0001c0001t0001g0028 | 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 | a0001c0001t0010g0180 | 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 | a0001c0001t0005g0159 | 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 | a0001c0001t0008g0160 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0071 | 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 | a0001c0002t0001g0010 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.131-975C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817053 | |||||||
| chrX:150817060 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150817351 | T | A | 1 | a0001c0001t0001g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.131-1273A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150817351 | |||||||
| chrX:150817532 | C | CT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0076 | 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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0072 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(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 | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
119 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(116): 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 | a0001c0001t0001g0022 a0001c0001t0001g0076 a0001c0001t0001g0129 others(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 | a0001c0001t0009g0197 a0001c0001t0017g0020 |
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 | a0001c0001t0001g0072 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0156 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0037 a0001c0001t0002g0153 a0001c0001t0002g0154 others(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 | a0001c0001t0006g0039 a0001c0002t0002g0011 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0009g0181 others(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 | a0001c0001t0001g0015 a0001c0001t0002g0013 a0001c0001t0008g0160 others(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 | a0001c0001t0002g0017 a0001c0001t0028g0070 a0001c0001t0035g0163 |
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 | a0001c0001t0001g0009 a0001c0001t0002g0005 a0001c0001t0002g0014 others(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 | a0001c0001t0011g0179 a0001c0001t0013g0073 a0001c0001t0025g0162 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0038g0178 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0072 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | a0001c0001t0001g0175 a0001c0001t0018g0101 a0001c0001t0018g0102 |
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 | a0001c0001t0001g0119 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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:150820055 | T | C | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150820406 | C | T | 4 | a0001c0001t0004g0030 a0001c0001t0004g0062 a0001c0001t0004g0201 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0072 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | a0001c0001t0009g0197 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0011g0124 | 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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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:150822746 | A | G | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150822907 | G | A | 1 | a0001c0001t0001g0072 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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:150823126 | A | T | 1 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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:150823746 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
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:150823804 | CATG | C | 2 | a0001c0001t0016g0068 a0001c0001t0016g0069 |
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:150824007 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0002g0034 a0001c0001t0002g0037 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0195 a0001c0001t0042g0211 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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:150824080 | GAAGAAGA others(3): Show |
G | 1 | a0001c0001t0004g0201 | 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 | AGAAGAAG | A | 12 | a0001c0001t0001g0031 a0001c0001t0001g0085 a0001c0001t0001g0090 others(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 | a0001c0001t0004g0201 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0002g0158 a0001c0001t0008g0157 |
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 | AAGG | A | 48 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0009g0192 | 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 | a0001c0001t0006g0194 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0005g0159 a0001c0001t0034g0149 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0024 | 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:150824177 | A | AAGG | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0136 a0001c0001t0001g0184 others(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:150824191 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
112 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(109): 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 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0002g0103 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0002g0103 |
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 | a0001c0001t0006g0194 | 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 | a0001c0001t0006g0194 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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:150824265 | A | AAGG | 8 | a0001c0001t0001g0119 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0119 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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:150824329 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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:150824341 | A | G | 4 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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:150824348 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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:150824372 | A | G | 1 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0119 a0001c0001t0004g0030 a0001c0001t0005g0204 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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:150824410 | AAAAGAAG others(3): Show |
A | 1 | a0001c0001t0001g0060 | 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 | G | 1 | a0001c0001t0001g0060 | 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 | GAGAAGAA others(13): Show |
1 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0119 | 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:150824437 | A | AAAGAAGA others(6): Show |
4 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0172 others(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 | G | 1 | a0001c0001t0001g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.130+6794T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824437 | |||||||
| chrX:150824444 | A | AAG | 3 | a0001c0001t0001g0059 a0001c0001t0001g0137 a0001c0001t0020g0057 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150824487 | GAAGAAGA others(3): Show |
G | 4 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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:150824497 | A | AAAG | 57 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150824498 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.130+6733T>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824498 | |||||||
| chrX:150824516 | G | A | 1 | a0001c0001t0009g0192 | 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 | a0001c0001t0009g0192 | 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 | a0001c0001t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6707T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824524 | |||||||
| chrX:150824534 | A | G | 1 | a0001c0001t0002g0046 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0173 a0001c0001t0040g0208 |
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:150824562 | A | AAGG | 22 | a0001c0001t0001g0072 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0009g0192 | 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 | a0001c0001t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6663C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824568 | |||||||
| chrX:150824571 | G | A | 1 | a0001c0001t0002g0046 | 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 | a0001c0001t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6657C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824574 | |||||||
| chrX:150824580 | G | A | 1 | a0001c0001t0002g0046 | 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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0002g0046 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.130+6645C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824586 | |||||||
| chrX:150824592 | A | G | 1 | a0001c0001t0002g0046 | 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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.130+6631C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150824600 | |||||||
| chrX:150824603 | G | A | 11 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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:150824643 | A | G | 1 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0007g0206 | 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:150824662 | A | AGAG | 7 | a0001c0001t0001g0048 a0001c0001t0004g0042 a0001c0001t0008g0120 others(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 | a0001c0001t0002g0063 a0001c0001t0002g0158 a0001c0001t0008g0157 others(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:150824674 | G | A | 12 | a0001c0001t0001g0048 a0001c0001t0002g0063 a0001c0001t0002g0158 others(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:150824683 | A | G | 12 | a0001c0001t0001g0048 a0001c0001t0002g0063 a0001c0001t0002g0158 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150824707 | G | A | 15 | a0001c0001t0001g0048 a0001c0001t0001g0087 a0001c0001t0002g0063 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
123 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(120): 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 | a0001c0001t0002g0093 a0001c0001t0017g0020 a0001c0001t0019g0115 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0009g0192 a0001c0001t0010g0019 a0001c0001t0010g0188 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150825549 | G | C | 48 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0003g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.130+5542A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150825689 | |||||||
| chrX:150825904 | A | C | 1 | a0001c0002t0001g0056 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0109 | 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 | a0001c0004t0001g0131 | 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 | a0001c0001t0038g0178 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0003g0174 | 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 | a0001c0001t0001g0190 a0001c0001t0006g0078 |
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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0037g0152 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0040g0208 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.130+1967T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829264 | |||||||
| chrX:150829692 | A | C | 1 | a0001c0002t0001g0021 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.130+1539T>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150829692 | |||||||
| chrX:150829909 | C | A | 1 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150830370 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.130+671delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 2/10 | chrX | 150830559 | |||||||
| chrX:150830651 | A | G | 1 | a0001c0001t0005g0205 | 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 | a0001c0001t0006g0041 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150831223 | C | T | 11 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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:150831712 | T | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.68-419A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150831712 | |||||||
| chrX:150831817 | A | G | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0016g0068 | 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 | a0001c0001t0009g0197 a0001c0001t0017g0196 |
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:150832846 | G | C | 1 | a0001c0001t0009g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.68-1553C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150832846 | |||||||
| chrX:150833054 | CA | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0033g0166 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-2370A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150833663 | |||||||
| chrX:150833950 | T | G | 14 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0004t0001g0131 | 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 | a0001c0001t0001g0184 a0001c0001t0032g0183 |
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 | a0001c0001t0002g0005 | 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 | a0001c0001t0013g0073 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.68-2958A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834251 | |||||||
| chrX:150834454 | T | C | 47 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.68-3390T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150834683 | |||||||
| chrX:150835155 | A | C | 4 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0173 a0001c0001t0040g0208 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0043g0210 | 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 | a0001c0001t0001g0119 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0002g0077 a0001c0001t0006g0041 |
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:150836348 | A | AT | 62 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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:150836431 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0187 a0001c0001t0004g0108 a0001c0001t0006g0194 others(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:150836994 | C | T | 1 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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:150837252 | A | AT | 5 | a0001c0001t0001g0072 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0190 a0001c0001t0002g0154 others(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 | a0001c0001t0001g0008 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.68-5979C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150837272 | |||||||
| chrX:150837987 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.68-6742C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838035 | |||||||
| chrX:150838391 | T | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150838678 | TA | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.68-7386delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838678 | |||||||
| chrX:150838678 | TAA | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0076 others(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:150838697 | A | G | 1 | a0001c0002t0001g0021 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.68-7404T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838697 | |||||||
| chrX:150838853 | C | T | 1 | a0001c0004t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.68-7560G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150838853 | |||||||
| chrX:150838898 | T | TA | 8 | a0001c0001t0001g0028 a0001c0001t0001g0119 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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:150838916 | AAT | A | 8 | a0001c0001t0001g0072 a0001c0001t0001g0123 a0001c0001t0007g0198 others(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 | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0002g0014 others(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 | a0001c0001t0008g0120 a0001c0001t0010g0180 |
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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0001t0001g0187 a0001c0001t0004g0108 a0001c0001t0006g0194 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0002g0014 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0066 others(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:150838919 | G | A | 2 | a0001c0001t0008g0120 a0001c0001t0010g0180 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0123 a0001c0001t0001g0187 others(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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0001t0008g0120 a0001c0001t0010g0180 |
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 | a0001c0001t0008g0176 a0001c0001t0019g0122 a0001c0002t0001g0121 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0119 others(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:150839716 | C | T | 1 | a0001c0001t0009g0181 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150839912 | C | T | 3 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0002t0001g0021 | 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 | a0001c0001t0025g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-8729T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840022 | |||||||
| chrX:150840074 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.68-8781C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840074 | |||||||
| chrX:150840225 | GAAAGAAA others(3): Show |
G | 3 | a0001c0001t0012g0164 a0001c0001t0012g0186 a0001c0001t0029g0126 |
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:150840271 | G | A | 4 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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:150840647 | A | G | 1 | a0001c0001t0002g0037 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150840876 | ATT | A | 3 | a0001c0001t0011g0124 a0001c0001t0011g0125 a0001c0001t0025g0162 |
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:150840973 | C | T | 1 | a0001c0001t0024g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-9680G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150840973 | |||||||
| chrX:150841219 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.68-9926C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841219 | |||||||
| chrX:150841292 | T | A | 1 | a0001c0001t0002g0046 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-9999A>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150841292 | |||||||
| chrX:150841640 | C | T | 1 | a0001c0001t0002g0046 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0016 a0001c0002t0002g0011 |
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 | a0001c0001t0001g0150 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0037g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.68-12419T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150843712 | |||||||
| chrX:150844610 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150845397 | G | A | 1 | a0001c0001t0010g0111 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0011g0179 | 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 | a0001c0002t0001g0203 | 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 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-14775G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150846068 | |||||||
| chrX:150847435 | T | C | 2 | a0001c0001t0018g0101 a0001c0001t0018g0102 |
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:150847847 | A | G | 1 | a0001c0001t0002g0103 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0189 others(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:150848118 | C | T | 4 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0138 |
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:150848328 | G | A | 5 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0001g0119 a0001c0001t0008g0120 a0001c0001t0008g0176 others(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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
135 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.68-17264dupT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150848556 | |||||||
| chrX:150848556 | TAA | T | 16 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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:150849077 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
88 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(85): 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0009g0197 a0001c0001t0017g0196 |
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 | a0001c0001t0004g0042 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0030g0040 | 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 | a0001c0001t0001g0156 a0001c0001t0002g0034 a0001c0001t0002g0037 others(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:150850914 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0019g0122 |
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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0155 a0001c0001t0037g0152 |
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 | a0001c0001t0004g0042 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0010g0111 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0002g0005 a0001c0001t0034g0149 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0003g0095 a0001c0001t0003g0141 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0048 |
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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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:150855511 | T | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0035g0163 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0002t0001g0203 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0002g0077 others(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 | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0173 a0001c0001t0040g0208 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0005g0159 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0085 a0001c0001t0001g0090 others(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:150859109 | A | T | 1 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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:150859499 | CT | C | 46 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0119 others(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 | CTTTTTTT others(1): Show |
C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0004g0135 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150860388 | A | G | 4 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | CAA | 7 | a0001c0001t0001g0123 a0001c0001t0002g0103 a0001c0001t0008g0120 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0156 a0001c0001t0009g0197 a0001c0001t0017g0196 others(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 | a0001c0001t0001g0109 a0001c0001t0002g0034 a0001c0001t0002g0110 others(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 | a0001c0001t0002g0037 a0001c0001t0007g0198 a0001c0001t0007g0200 others(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 | a0001c0001t0001g0107 a0001c0001t0006g0039 a0001c0001t0013g0033 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0187 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0032 | 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 | a0001c0001t0042g0211 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0007g0206 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-30596C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150861889 | |||||||
| chrX:150861905 | CA | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0087 a0001c0001t0001g0173 others(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:150861917 | AAGAG | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0002t0001g0203 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0002g0005 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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:150862850 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.68-31557C>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150862850 | |||||||
| chrX:150862862 | G | A | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | GAAAGA | 4 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0107 a0001c0001t0006g0039 a0001c0001t0009g0192 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0015g0151 | 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 | a0001c0001t0024g0193 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0011g0179 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0150 a0001c0001t0001g0189 others(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:150865964 | T | C | 4 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0042g0211 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0011g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67+31867G>A | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150866655 | |||||||
| chrX:150867077 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0008g0157 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0010g0188 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67+30714C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150867808 | |||||||
| chrX:150867892 | CA | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0187 a0001c0001t0004g0108 others(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 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0036g0161 | 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 | 14 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0038 others(11): Show |
15 | HG00741.hp1 HG01069.hp1 HG01256.hp1 others(12): 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 | a0001c0001t0001g0085 a0001c0001t0005g0202 a0001c0001t0020g0057 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0036g0161 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0010g0111 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0034g0149 others(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 | a0001c0001t0004g0108 a0001c0001t0011g0179 a0001c0001t0026g0167 |
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:150870048 | G | A | 1 | a0001c0001t0009g0192 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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 | a0001c0001t0043g0210 | 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 | a0003c0003t0012g0148 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0009g0165 a0001c0001t0012g0164 a0001c0001t0012g0186 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0002t0001g0121 | 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 | a0001c0001t0011g0179 | 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 | a0001c0001t0030g0040 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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:150872360 | T | G | 1 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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:150872661 | TA | T | 25 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0195 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0195 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150873738 | A | G | 1 | a0001c0001t0003g0174 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0014g0105 a0001c0001t0014g0117 a0001c0001t0014g0118 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150875096 | T | C | 2 | a0001c0001t0021g0127 a0001c0001t0021g0168 |
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 | a0001c0001t0023g0006 | 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 | a0001c0001t0019g0115 | 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0156 a0001c0001t0002g0034 a0001c0001t0002g0037 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0016g0069 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0123 others(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:150877134 | A | G | 1 | a0001c0001t0009g0165 | 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 | a0001c0001t0003g0191 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150877600 | T | C | 59 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0006g0041 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0106 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0195 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0001g0099 a0001c0001t0007g0200 a0001c0001t0009g0197 others(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 | a0001c0001t0034g0149 | 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 | TAC | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
81 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(78): 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 | TACAC | T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0017g0020 a0001c0001t0030g0040 a0001c0001t0039g0007 |
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 | a0001c0001t0004g0201 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0156 others(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:150878533 | T | TAA | 6 | a0001c0001t0001g0119 a0001c0001t0001g0195 a0001c0001t0008g0120 others(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 | TA | T | 11 | a0001c0001t0001g0106 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0195 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0038g0178 | 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 | a0001c0001t0011g0179 | 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 | a0001c0001t0001g0195 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0008g0176 | 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 | a0001c0001t0001g0119 a0001c0001t0008g0120 a0001c0001t0008g0176 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0195 a0001c0001t0005g0204 others(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 | a0001c0001t0034g0149 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0032 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | TTAA | 8 | a0001c0001t0001g0187 a0001c0001t0004g0108 a0001c0001t0006g0194 others(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 | TA | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0104 a0001c0001t0001g0113 others(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:150879783 | G | A | 11 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | a0001c0001t0003g0174 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0050 others(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 | CAAA | 6 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0008g0120 others(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:150880256 | A | G | 1 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0016 a0001c0002t0002g0011 |
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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0002g0017 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+16982A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150881540 | |||||||
| chrX:150881808 | C | T | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(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 | AT | A | 9 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0156 others(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:150881844 | G | A | 1 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0195 |
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 | a0001c0001t0011g0124 a0001c0001t0011g0125 a0001c0001t0025g0162 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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:150883063 | G | A | 1 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0195 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0032 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.67+14850A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883672 | |||||||
| chrX:150883715 | T | C | 1 | a0001c0001t0003g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67+14807A>G | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150883715 | |||||||
| chrX:150884012 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0013g0073 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0012g0186 a0001c0001t0029g0126 |
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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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:150885382 | A | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150885492 | G | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0019g0115 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0002g0158 a0001c0001t0008g0157 a0001c0001t0016g0068 others(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 | a0001c0001t0003g0174 | 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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0003g0130 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0001 a0001c0001t0004g0201 a0001c0001t0005g0204 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | 48 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(45): Show |
48 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.67+11380delT | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887141 | |||||||
| chrX:150887283 | T | C | 1 | a0001c0001t0003g0143 | 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 | a0001c0001t0005g0159 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150887449 | G | GAAAT | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0189 a0001c0001t0004g0108 others(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 | GAAATAAA others(5): Show |
G | 1 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+10773C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150887749 | |||||||
| chrX:150888006 | G | GTGCGGCA others(15): Show |
21 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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:150888477 | T | C | 3 | a0001c0001t0011g0124 a0001c0001t0011g0125 a0001c0001t0025g0162 |
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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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:150888910 | C | T | 51 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0042g0211 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0002g0063 a0001c0001t0007g0206 a0001c0001t0031g0114 |
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 | TAA | 14 | a0001c0001t0001g0119 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0123 a0001c0001t0038g0178 |
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:150889508 | G | A | 3 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 |
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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150889959 | T | C | 52 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0008g0120 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0195 a0001c0001t0005g0204 others(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 | AAAATAAA others(5): Show |
2 | a0001c0001t0008g0120 a0001c0001t0019g0122 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0195 a0001c0001t0005g0204 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150890307 | C | T | 3 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150890913 | C | A | 3 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0024g0193 | 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 | a0001c0001t0007g0198 a0001c0001t0007g0199 a0001c0001t0007g0200 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0119 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150892335 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.67+6187C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150892335 | |||||||
| chrX:150892605 | C | CA | 16 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0038 others(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 | CA | C | 61 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0004g0030 a0001c0001t0004g0062 a0001c0001t0004g0201 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0119 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | a0001c0001t0001g0119 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | a0001c0001t0021g0127 a0001c0001t0021g0168 |
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 | a0001c0001t0002g0158 a0001c0001t0008g0157 a0001c0001t0016g0068 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150893835 | C | T | 2 | a0001c0001t0001g0107 a0002c0005t0041g0209 |
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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0008g0120 a0001c0001t0008g0176 a0001c0001t0019g0122 others(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 | a0001c0001t0001g0195 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
141 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(138): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0007g0198 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0018 a0001c0001t0002g0017 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0006g0194 a0001c0001t0009g0192 a0001c0001t0024g0193 |
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 | a0001c0001t0011g0179 | 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 | a0001c0001t0001g0175 a0001c0001t0018g0101 a0001c0001t0018g0102 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0195 a0001c0001t0005g0204 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0008g0160 | 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 | CAA | 12 | a0001c0001t0001g0119 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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:150896074 | A | C | 13 | a0001c0001t0001g0106 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0195 a0001c0001t0005g0204 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0003c0003t0012g0148 | 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 | a0001c0001t0001g0195 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+1552T>C | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150896970 | |||||||
| chrX:150897314 | A | G | 1 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0207 a0001c0001t0005g0204 a0001c0001t0005g0205 others(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 | a0001c0001t0001g0195 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | a0001c0001t0007g0206 a0001c0002t0001g0203 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150897604 | A | G | 1 | a0001c0001t0001g0150 | 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 | a0001c0001t0042g0211 a0001c0001t0043g0210 |
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 | a0001c0001t0042g0211 | 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 | a0001c0001t0001g0104 a0001c0001t0002g0103 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0002g0064 |
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 | 38 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): Show |
38 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.67+467dupG | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898054 | |||||||
| chrX:150898054 | A | ACC | 34 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | AC | A | 26 | a0001c0001t0001g0150 a0001c0001t0001g0156 a0001c0001t0001g0170 others(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 | ACCC | A | 15 | a0001c0001t0001g0195 a0001c0001t0005g0177 a0001c0001t0005g0204 others(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 | ACCCCCC | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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:150898061 | C | G | 8 | a0001c0001t0001g0195 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | a0001c0001t0001g0195 a0001c0001t0007g0198 a0001c0001t0007g0199 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0004g0201 | 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 | a0001c0001t0005g0202 | 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 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0002t0001g0203 |
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 | a0001c0001t0007g0206 | 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 | a0001c0001t0001g0207 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.67+220C>T | CD99L2 | ENSG00000102181.22 | transcript | ENST00000370377.8 | protein_coding | 1/10 | chrX | 150898302 |