Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11326 |
| ensemblid | ENSG00000155659.15 |
| hgncid | 17032 |
| symbol | VSIG4 |
| name | V-set and immunoglobulin domain containing 4 |
| refseq_nuc | NM_007268.3 |
| refseq_prot | NP_009199.1 |
| ensembl_nuc | ENST00000374737.9 |
| ensembl_prot | ENSP00000363869.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 66021738 |
| end | 66040080 |
| strand | - |
| ver | v1.2 |
| region | chrX:66021738-66040080 |
| region5000 | chrX:66016738-66045080 |
| regionname0 | VSIG4_chrX_66021738_66040080 |
| regionname5000 | VSIG4_chrX_66016738_66045080 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 399 | 208 | 40 | 41 | 84 | 11 | 30 | 64 | VSIG4_chrX_66016738_66045080 | VSIG4 | MGILL others(394): Show |
chrX | 66016738 | 66045080 |
| a0002 | 0/0 | 399 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | MGILL others(394): Show |
chrX | 66016738 | 66045080 |
| a0003 | 0/0 | 399 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | MGILL others(394): Show |
chrX | 66016738 | 66045080 |
| a0004 | 0/0 | 399 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | MGILL others(394): Show |
chrX | 66016738 | 66045080 |
| a0005 | 0/0 | 399 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | MGILL others(394): Show |
chrX | 66016738 | 66045080 |
| a0006 | 0/0 | 399 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | MGILL others(394): Show |
chrX | 66016738 | 66045080 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1197 | 205 | 39 | 39 | 84 | 11 | 30 | VSIG4_chrX_66016738_66045080 | VSIG4 | ATGGG others(1192): Show |
chrX | 66016738 | 66045080 | ||
| a0001c0004 | 0/0 | 1197 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ATGGG others(1192): Show |
chrX | 66016738 | 66045080 | ||
| a0001c0007 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ATGGG others(1192): Show |
chrX | 66016738 | 66045080 | ||
| a0002c0002 | 0/0 | 1197 | 4 | 2 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ATGGG others(1192): Show |
chrX | 66016738 | 66045080 | ||
| a0003c0005 | 0/0 | 1197 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ATGGG others(1192): Show |
chrX | 66016738 | 66045080 | ||
| a0004c0003 | 0/0 | 1197 | 2 | 0 | 0 | 0 | 0 | 2 | VSIG4_chrX_66016738_66045080 | VSIG4 | ATGGG others(1192): Show |
chrX | 66016738 | 66045080 | ||
| a0005c0006 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ATGGG others(1192): Show |
chrX | 66016738 | 66045080 | ||
| a0006c0008 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ATGGG others(1192): Show |
chrX | 66016738 | 66045080 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1807 | 182 | 30 | 35 | 77 | 10 | 28 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0001c0001t0002 | 0/0 | 1807 | 7 | 6 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0001c0001t0003 | 0/0 | 1807 | 7 | 0 | 0 | 7 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0001c0001t0004 | 0/0 | 1807 | 5 | 0 | 4 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0001c0001t0005 | 0/0 | 1807 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0001c0001t0006 | 0/0 | 1807 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0001c0001t0007 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0001c0004t0001 | 0/0 | 1807 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0001c0007t0001 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0002c0002t0001 | 0/0 | 1807 | 4 | 2 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0003c0005t0001 | 0/0 | 1807 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0004c0003t0001 | 0/0 | 1807 | 2 | 0 | 0 | 0 | 0 | 2 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0005c0006t0001 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| a0006c0008t0001 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | ACAGA others(1802): Show |
chrX | 66016738 | 66045080 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 0 | 1 | 16 | 0 | 8 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0004g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0004t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0001c0007t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0003c0005t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0003c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0004c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0005c0006t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| a0006c0008t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00733 | hp2 | a0003 | c0005 | t0001 | g0134 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01168 | hp1 | a0001 | c0004 | t0001 | g0023 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01168 | hp2 | a0003 | c0005 | t0001 | g0135 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02647 | hp1 | a0001 | c0007 | t0001 | g0152 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0077 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03130 | hp1 | a0005 | c0006 | t0001 | g0143 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03704 | hp2 | a0004 | c0003 | t0001 | g0015 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03831 | hp2 | a0004 | c0003 | t0001 | g0015 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | CHB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18957 | hp1 | a0006 | c0008 | t0001 | g0086 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | LWK | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0041 | REF | REF | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0104 | REF | REF | VSIG4_chrX_66016738_66045080 | VSIG4 | chrX | 66016738 | 66045080 |
| 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:66022315 | G | A | 1 | a0003 | 2 | HG00733.hp2 HG01168.hp2 |
missense_variant | MODERATE | c.1148C>T | p.Thr383Ile | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 1230/1807 | 1148/1200 | 383/399 | chrX | 66022315 | |||
| chrX:66025057 | T | C | 1 | a0002 | 4 | HG01167.hp1 HG01169.hp1 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.908A>G | p.Tyr303Cys | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/8 | 990/1807 | 908/1200 | 303/399 | chrX | 66025057 | |||
| chrX:66025129 | C | T | 1 | a0004 | 2 | HG03704.hp2 HG03831.hp2 |
missense_variant&splice_region_variant | MODERATE | c.836G>A | p.Gly279Glu | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/8 | 918/1807 | 836/1200 | 279/399 | chrX | 66025129 | |||
| chrX:66032581 | C | T | 1 | a0005 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.581G>A | p.Ser194Asn | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/8 | 663/1807 | 581/1200 | 194/399 | chrX | 66032581 | |||
| chrX:66033513 | C | A | 1 | a0006 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.373G>T | p.Val125Phe | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/8 | 455/1807 | 373/1200 | 125/399 | chrX | 66033513 | |||
| chrX:66033612 | C | A | 1 | a0003 | 2 | HG00733.hp2 HG01168.hp2 |
missense_variant | MODERATE | c.274G>T | p.Val92Phe | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/8 | 356/1807 | 274/1200 | 92/399 | chrX | 66033612 |
| 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:66022389 | A | T | 1 | a0001c0004 | 2 | HG01168.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1074T>A | p.Ser358Ser | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 1156/1807 | 1074/1200 | 358/399 | chrX | 66022389 | |||
| chrX:66032559 | C | T | 1 | a0001c0007 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.603G>A | p.Ala201Ala | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/8 | 685/1807 | 603/1200 | 201/399 | chrX | 66032559 |
| 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:66021884 | G | A | 1 | a0001c0001t0004 | 5 | HG00735.hp2 HG01109.hp1 HG01346.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*379C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 379 | chrX | 66021884 | ||||||
| chrX:66021926 | G | T | 1 | a0001c0001t0003 | 7 | HG00621.hp1 HG02132.hp1 NA18747.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*337C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 337 | chrX | 66021926 | ||||||
| chrX:66022026 | G | T | 1 | a0001c0001t0007 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*237C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 237 | chrX | 66022026 | ||||||
| chrX:66022116 | C | T | 1 | a0001c0001t0006 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*147G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 147 | chrX | 66022116 | ||||||
| chrX:66022135 | C | A | 1 | a0001c0001t0005 | 2 | HG02615.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*128G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 8/8 | 128 | chrX | 66022135 | ||||||
| chrX:66040051 | C | T | 1 | a0001c0001t0002 | 7 | HG01516.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-53G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/8 | 53 | chrX | 66040051 |
| 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:66022509 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.963-9G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 7/7 | chrX | 66022509 | |||||||
| chrX:66022650 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0130 |
2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.963-150G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 7/7 | chrX | 66022650 | |||||||
| chrX:66022667 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.963-167G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 7/7 | chrX | 66022667 | |||||||
| chrX:66023112 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.941-250C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023112 | |||||||
| chrX:66023282 | C | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.941-420G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023282 | |||||||
| chrX:66023421 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.941-559T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023421 | |||||||
| chrX:66023483 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.941-621C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023483 | |||||||
| chrX:66023484 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.941-622G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023484 | |||||||
| chrX:66023880 | G | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.941-1018C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66023880 | |||||||
| chrX:66024093 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0112 |
3 | NA18975.hp2 NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.940+932C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024093 | |||||||
| chrX:66024220 | T | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0033 others(36): Show |
44 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.940+805A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024220 | |||||||
| chrX:66024590 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.940+435G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024590 | |||||||
| chrX:66024749 | G | C | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.940+276C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024749 | |||||||
| chrX:66024808 | A | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0051 others(4): Show |
8 | NA18947.hp1 NA18954.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.940+217T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 6/7 | chrX | 66024808 | |||||||
| chrX:66025263 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0080 |
2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.836-134G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66025263 | |||||||
| chrX:66025940 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.836-811T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66025940 | |||||||
| chrX:66026027 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.836-898G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026027 | |||||||
| chrX:66026520 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835+929C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026520 | |||||||
| chrX:66026663 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.835+786G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026663 | |||||||
| chrX:66026715 | A | ATTTAATT others(140): Show |
1 | a0001c0001t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.835+733_835+734ins others(147): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026715 | |||||||
| chrX:66026730 | G | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.835+719C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026730 | |||||||
| chrX:66026857 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0080 |
2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.835+592T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026857 | |||||||
| chrX:66026933 | T | A | 2 | a0001c0001t0003g0144 a0001c0001t0003g0145 |
2 | NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.835+516A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66026933 | |||||||
| chrX:66027252 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.835+197C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66027252 | |||||||
| chrX:66027259 | T | C | 52 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(49): Show |
60 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.835+190A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66027259 | |||||||
| chrX:66027414 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.835+35T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 5/7 | chrX | 66027414 | |||||||
| chrX:66027567 | T | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(47): Show |
56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.758-41A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027567 | |||||||
| chrX:66027727 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.758-201A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027727 | |||||||
| chrX:66027776 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.758-250T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027776 | |||||||
| chrX:66027860 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.757+190C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027860 | |||||||
| chrX:66027968 | CCATGGCA others(7): Show |
C | 1 | a0001c0001t0001g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.757+68_757+81delAT others(12): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 4/7 | chrX | 66027968 | |||||||
| chrX:66028151 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-39G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028151 | |||||||
| chrX:66028193 | G | A | 2 | a0002c0002t0001g0018 a0002c0002t0001g0019 |
4 | HG01167.hp1 HG01169.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-81C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028193 | |||||||
| chrX:66028326 | G | A | 1 | a0001c0001t0005g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.695-214C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028326 | |||||||
| chrX:66028363 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-251G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028363 | |||||||
| chrX:66028377 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.695-265A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028377 | |||||||
| chrX:66028378 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.695-266T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028378 | |||||||
| chrX:66028550 | G | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0033 others(36): Show |
44 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.695-438C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028550 | |||||||
| chrX:66028558 | C | CT | 10 | a0001c0001t0001g0056 a0001c0001t0001g0065 a0001c0001t0001g0068 others(7): Show |
10 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-447dupA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | |||||||
| chrX:66028558 | C | CTT | 5 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0001g0101 others(2): Show |
5 | HG02055.hp1 HG02074.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-448_695-447dup others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | |||||||
| chrX:66028558 | CT | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0037 others(42): Show |
50 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.695-447delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | |||||||
| chrX:66028558 | CTT | C | 9 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0141 others(6): Show |
11 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.695-448_695-447del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028558 | |||||||
| chrX:66028589 | T | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
8 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.695-477A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028589 | |||||||
| chrX:66028616 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.695-504G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028616 | |||||||
| chrX:66028695 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0087 |
4 | HG01361.hp2 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-583A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66028695 | |||||||
| chrX:66029097 | T | C | 50 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(47): Show |
56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.695-985A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029097 | |||||||
| chrX:66029104 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.695-992G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029104 | |||||||
| chrX:66029132 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-1020C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029132 | |||||||
| chrX:66029146 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0082 |
5 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-1034C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029146 | |||||||
| chrX:66029260 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.695-1148C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029260 | |||||||
| chrX:66029469 | A | T | 1 | a0001c0001t0001g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.695-1357T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029469 | |||||||
| chrX:66029538 | G | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.695-1426C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029538 | |||||||
| chrX:66029590 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.695-1478T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029590 | |||||||
| chrX:66029593 | T | A | 7 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(4): Show |
7 | HG01516.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-1481A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029593 | |||||||
| chrX:66029762 | A | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(47): Show |
56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.695-1650T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029762 | |||||||
| chrX:66029809 | G | A | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
13 | HG00738.hp1 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-1697C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029809 | |||||||
| chrX:66029884 | G | GA | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.695-1773dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029884 | |||||||
| chrX:66029890 | AT | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.695-1779delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029890 | |||||||
| chrX:66029891 | T | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(47): Show |
58 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.695-1779A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66029891 | |||||||
| chrX:66030346 | T | C | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+2122A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030346 | |||||||
| chrX:66030360 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.694+2108C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030360 | |||||||
| chrX:66030383 | ACATATAT others(6): Show |
A | 1 | a0001c0001t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.694+2072_694+2084d others(15): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030383 | |||||||
| chrX:66030483 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.694+1985C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030483 | |||||||
| chrX:66030589 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.694+1879T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030589 | |||||||
| chrX:66030740 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.694+1728T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030740 | |||||||
| chrX:66030839 | C | T | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
13 | HG00738.hp1 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.694+1629G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030839 | |||||||
| chrX:66030894 | A | G | 26 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 others(23): Show |
28 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.694+1574T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030894 | |||||||
| chrX:66030953 | G | A | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.694+1515C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66030953 | |||||||
| chrX:66031208 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.694+1260G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031208 | |||||||
| chrX:66031295 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.694+1173G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031295 | |||||||
| chrX:66031306 | C | T | 2 | a0001c0001t0003g0144 a0001c0001t0003g0145 |
2 | NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.694+1162G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031306 | |||||||
| chrX:66031322 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.694+1146A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031322 | |||||||
| chrX:66031369 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.694+1099C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031369 | |||||||
| chrX:66031582 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.694+886A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031582 | |||||||
| chrX:66031992 | G | A | 1 | a0006c0008t0001g0086 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.694+476C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66031992 | |||||||
| chrX:66032126 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0126 |
5 | HG02965.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.694+342G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032126 | |||||||
| chrX:66032209 | T | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.694+259A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032209 | |||||||
| chrX:66032236 | C | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.694+232G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032236 | |||||||
| chrX:66032244 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.694+224A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032244 | |||||||
| chrX:66032373 | T | TCTCCCAA others(6): Show |
1 | a0001c0001t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.694+82_694+94dupGA others(11): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 3/7 | chrX | 66032373 | |||||||
| chrX:66032759 | A | C | 1 | a0001c0001t0001g0012 | 2 | HG02071.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.413-10T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66032759 | |||||||
| chrX:66032837 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0087 |
4 | HG01361.hp2 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-88G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66032837 | |||||||
| chrX:66032857 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.413-108C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66032857 | |||||||
| chrX:66032891 | A | G | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-142T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66032891 | |||||||
| chrX:66033012 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.413-263C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033012 | |||||||
| chrX:66033111 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0109 |
2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.413-362G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033111 | |||||||
| chrX:66033156 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.412+318G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033156 | |||||||
| chrX:66033204 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | NA18947.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.412+270C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033204 | |||||||
| chrX:66033369 | G | A | 1 | a0001c0007t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.412+105C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033369 | |||||||
| chrX:66033389 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.412+85G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 2/7 | chrX | 66033389 | |||||||
| chrX:66033841 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0007g0060 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.56-11C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033841 | |||||||
| chrX:66033842 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-12C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033842 | |||||||
| chrX:66033879 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.56-49G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033879 | |||||||
| chrX:66033927 | T | C | 50 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(47): Show |
56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.56-97A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033927 | |||||||
| chrX:66033954 | T | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0033 others(29): Show |
37 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.56-124A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66033954 | |||||||
| chrX:66034526 | T | A | 1 | a0001c0001t0001g0004 | 4 | HG02965.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-696A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034526 | |||||||
| chrX:66034704 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.56-874C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034704 | |||||||
| chrX:66034766 | T | G | 1 | a0001c0001t0001g0051 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-936A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034766 | |||||||
| chrX:66034766 | T | TG | 12 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0034 others(9): Show |
17 | HG01346.hp2 HG01516.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.56-937dupC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034766 | |||||||
| chrX:66034770 | GGT | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(36): Show |
46 | HG00733.hp2 HG00738.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.56-942_56-941delAC | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034770 | |||||||
| chrX:66034771 | GT | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(30): Show |
41 | HG00438.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.56-942delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034771 | |||||||
| chrX:66034772 | T | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(49): Show |
71 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.56-942A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034772 | |||||||
| chrX:66034777 | G | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.56-947C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66034777 | |||||||
| chrX:66035228 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.56-1398G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035228 | |||||||
| chrX:66035522 | T | C | 1 | a0001c0001t0001g0004 | 4 | HG02965.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-1692A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035522 | |||||||
| chrX:66035623 | C | A | 4 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-1793G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66035623 | |||||||
| chrX:66036139 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.56-2309A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036139 | |||||||
| chrX:66036148 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56-2318A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036148 | |||||||
| chrX:66036191 | C | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.56-2361G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036191 | |||||||
| chrX:66036274 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.56-2444C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036274 | |||||||
| chrX:66036394 | T | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0033 others(35): Show |
43 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.56-2564A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036394 | |||||||
| chrX:66036493 | T | A | 1 | a0001c0001t0001g0051 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.56-2663A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036493 | |||||||
| chrX:66036520 | G | C | 2 | a0002c0002t0001g0018 a0002c0002t0001g0019 |
4 | HG01167.hp1 HG01169.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-2690C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036520 | |||||||
| chrX:66036635 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2805C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036635 | |||||||
| chrX:66036638 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2808T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036638 | |||||||
| chrX:66036654 | AAT | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-2826_56-2825del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036654 | |||||||
| chrX:66036657 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2827T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036657 | |||||||
| chrX:66036662 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2832T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036662 | |||||||
| chrX:66036667 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0002g0025 |
2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-2837T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036667 | |||||||
| chrX:66036668 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2838A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036668 | |||||||
| chrX:66036671 | AAT | A | 2 | a0001c0001t0003g0144 a0001c0001t0003g0145 |
2 | NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.56-2843_56-2842del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036671 | |||||||
| chrX:66036672 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2842T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036672 | |||||||
| chrX:66036678 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2848T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036678 | |||||||
| chrX:66036680 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2850T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036680 | |||||||
| chrX:66036681 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2851T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036681 | |||||||
| chrX:66036684 | C | T | 4 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0002g0025 others(1): Show |
4 | HG00738.hp1 HG01081.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-2854G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036684 | |||||||
| chrX:66036685 | G | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2855C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036685 | |||||||
| chrX:66036691 | T | A | 2 | a0001c0001t0001g0098 a0001c0001t0002g0025 |
2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-2861A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036691 | |||||||
| chrX:66036692 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2862A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036692 | |||||||
| chrX:66036694 | T | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(43): Show |
54 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.56-2864A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036694 | |||||||
| chrX:66036697 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0002g0025 |
2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-2867T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036697 | |||||||
| chrX:66036703 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2873A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036703 | |||||||
| chrX:66036703 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2873A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036703 | |||||||
| chrX:66036709 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2879A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036709 | |||||||
| chrX:66036714 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2884T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036714 | |||||||
| chrX:66036718 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2888A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036718 | |||||||
| chrX:66036725 | T | TATATAAT others(41): Show |
3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.56-2896_56-2895ins others(48): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036725 | |||||||
| chrX:66036730 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2900T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036730 | |||||||
| chrX:66036743 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2913A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036743 | |||||||
| chrX:66036749 | T | TATATA | 1 | a0002c0002t0001g0019 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.56-2924_56-2920dup others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036749 | |||||||
| chrX:66036749 | TATATA | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0113 |
2 | NA19007.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.56-2924_56-2920del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036749 | |||||||
| chrX:66036754 | A | C | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2924T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036754 | |||||||
| chrX:66036754 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2924T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036754 | |||||||
| chrX:66036759 | A | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0070 a0001c0001t0001g0148 others(5): Show |
9 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-2929T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036759 | |||||||
| chrX:66036766 | T | TATATAAT others(3): Show |
1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2937_56-2936ins others(10): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036766 | |||||||
| chrX:66036768 | T | TATATTAT others(32): Show |
1 | a0001c0001t0002g0029 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.56-2977_56-2939dup others(39): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036768 | |||||||
| chrX:66036770 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2940A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036770 | |||||||
| chrX:66036771 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2941T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036771 | |||||||
| chrX:66036772 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2942A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036772 | |||||||
| chrX:66036772 | T | TATTA | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2943_56-2942ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036772 | |||||||
| chrX:66036773 | T | C | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2943A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036773 | |||||||
| chrX:66036775 | T | TA | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2946dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036775 | |||||||
| chrX:66036777 | T | TTATATTA others(32): Show |
1 | a0001c0001t0002g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56-2948_56-2947ins others(39): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036777 | |||||||
| chrX:66036778 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2948A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036778 | |||||||
| chrX:66036782 | T | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2952A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036782 | |||||||
| chrX:66036783 | T | A | 2 | a0001c0001t0001g0098 a0001c0001t0002g0025 |
2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-2953A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036783 | |||||||
| chrX:66036785 | TATATA | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.56-2960_56-2956del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036785 | |||||||
| chrX:66036787 | T | TTA | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2958_56-2957ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036787 | |||||||
| chrX:66036790 | A | AATATAAT others(24): Show |
1 | a0001c0001t0001g0024 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.56-2961_56-2960ins others(31): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036790 | |||||||
| chrX:66036792 | TA | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0126 |
5 | HG02965.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-2963delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036792 | |||||||
| chrX:66036793 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2963T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036793 | |||||||
| chrX:66036796 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2966T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036796 | |||||||
| chrX:66036797 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2967A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036797 | |||||||
| chrX:66036801 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2971A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036801 | |||||||
| chrX:66036802 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-2972A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036802 | |||||||
| chrX:66036807 | A | C | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-2977T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036807 | |||||||
| chrX:66036807 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2977T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036807 | |||||||
| chrX:66036810 | AT | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2981delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036810 | |||||||
| chrX:66036812 | T | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0150 a0001c0001t0002g0025 |
3 | HG01358.hp1 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.56-2982A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036812 | |||||||
| chrX:66036813 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2983T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036813 | |||||||
| chrX:66036817 | AT | A | 3 | a0001c0001t0002g0025 a0001c0001t0005g0035 a0001c0001t0005g0036 |
3 | HG02572.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.56-2988delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036817 | |||||||
| chrX:66036818 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2988A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036818 | |||||||
| chrX:66036822 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2992A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036822 | |||||||
| chrX:66036823 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-2993T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036823 | |||||||
| chrX:66036826 | T | TG | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-2997_56-2996ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036826 | |||||||
| chrX:66036832 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3002T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036832 | |||||||
| chrX:66036836 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-3006C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036836 | |||||||
| chrX:66036837 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3007A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036837 | |||||||
| chrX:66036838 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-3008A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036838 | |||||||
| chrX:66036842 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.56-3012A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036842 | |||||||
| chrX:66036843 | A | C | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3013T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036843 | |||||||
| chrX:66036843 | A | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03041.hp2 HG03195.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-3013T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036843 | |||||||
| chrX:66036844 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-3014T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036844 | |||||||
| chrX:66036845 | T | A | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-3015A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036845 | |||||||
| chrX:66036845 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.56-3015A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036845 | |||||||
| chrX:66036846 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-3016T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036846 | |||||||
| chrX:66036849 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3019A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036849 | |||||||
| chrX:66036850 | T | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3020A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036850 | |||||||
| chrX:66036854 | T | TA | 2 | a0001c0001t0001g0150 a0001c0001t0001g0158 |
2 | HG02004.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.56-3025dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036854 | |||||||
| chrX:66036858 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3028A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036858 | |||||||
| chrX:66036859 | A | AATAATAT others(34): Show |
1 | a0001c0001t0003g0099 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.55+3044_56-3030dup others(41): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036859 | |||||||
| chrX:66036859 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3029T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036859 | |||||||
| chrX:66036868 | T | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0002g0025 |
3 | HG02055.hp1 HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.56-3038A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036868 | |||||||
| chrX:66036869 | T | A | 14 | a0001c0001t0001g0039 a0001c0001t0001g0121 a0001c0001t0001g0132 others(11): Show |
15 | HG00733.hp2 HG01168.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.56-3039A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036869 | |||||||
| chrX:66036873 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3043A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036873 | |||||||
| chrX:66036874 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3044A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036874 | |||||||
| chrX:66036874 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-3044A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036874 | |||||||
| chrX:66036874 | T | TATATATT others(22): Show |
3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+3041_56-3045dup others(29): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036874 | |||||||
| chrX:66036878 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.56-3048A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036878 | |||||||
| chrX:66036880 | T | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-3050A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036880 | |||||||
| chrX:66036885 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-3055A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036885 | |||||||
| chrX:66036886 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56-3056A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036886 | |||||||
| chrX:66036892 | T | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02055.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3052A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036892 | |||||||
| chrX:66036893 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+3051A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036893 | |||||||
| chrX:66036894 | T | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02572.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3050A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036894 | |||||||
| chrX:66036894 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+3050A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036894 | |||||||
| chrX:66036897 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+3047A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036897 | |||||||
| chrX:66036898 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3046A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036898 | |||||||
| chrX:66036904 | ATATATTA others(10): Show |
A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0033 others(35): Show |
43 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.55+3023_55+3039del others(17): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036904 | |||||||
| chrX:66036909 | T | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0002g0025 |
3 | HG02572.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3035A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036909 | |||||||
| chrX:66036910 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+3034A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036910 | |||||||
| chrX:66036915 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3029C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036915 | |||||||
| chrX:66036915 | G | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
4 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3029C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036915 | |||||||
| chrX:66036918 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3026T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036918 | |||||||
| chrX:66036921 | T | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0148 others(1): Show |
4 | HG03041.hp2 HG03195.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3023A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036921 | |||||||
| chrX:66036921 | TTATATTA others(5): Show |
T | 1 | a0001c0001t0001g0007 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.55+3011_55+3022del others(12): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036921 | |||||||
| chrX:66036922 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+3022A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036922 | |||||||
| chrX:66036926 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3018A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036926 | |||||||
| chrX:66036926 | T | TAATAATA others(3): Show |
1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+3017_55+3018ins others(10): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036926 | |||||||
| chrX:66036927 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+3017A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036927 | |||||||
| chrX:66036927 | T | G | 3 | a0001c0001t0003g0145 a0001c0001t0004g0006 a0001c0001t0004g0011 |
6 | HG00735.hp2 HG01109.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+3017A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036927 | |||||||
| chrX:66036932 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0002g0025 |
2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.55+3012C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036932 | |||||||
| chrX:66036932 | G | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3012C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036932 | |||||||
| chrX:66036937 | AT | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+3006delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036937 | |||||||
| chrX:66036938 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0002g0025 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+3006A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036938 | |||||||
| chrX:66036944 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0002g0025 |
3 | HG02055.hp1 HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.55+3000C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036944 | |||||||
| chrX:66036944 | G | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03041.hp2 HG03195.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.55+3000C>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036944 | |||||||
| chrX:66036945 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2999T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036945 | |||||||
| chrX:66036946 | T | TATA | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2995_55+2997dup others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036946 | |||||||
| chrX:66036950 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2994A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036950 | |||||||
| chrX:66036951 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0002g0025 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+2993A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036951 | |||||||
| chrX:66036955 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2989A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036955 | |||||||
| chrX:66036956 | T | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0098 a0001c0001t0001g0150 |
3 | HG02055.hp1 HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.55+2988A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036956 | |||||||
| chrX:66036958 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.55+2986A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036958 | |||||||
| chrX:66036961 | T | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0150 |
2 | HG02055.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.55+2983A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036961 | |||||||
| chrX:66036961 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2983A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036961 | |||||||
| chrX:66036961 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+2983A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036961 | |||||||
| chrX:66036963 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2981A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036963 | |||||||
| chrX:66036965 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2979A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036965 | |||||||
| chrX:66036966 | A | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0098 |
2 | HG02683.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.55+2978T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036966 | |||||||
| chrX:66036967 | A | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2977T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036967 | |||||||
| chrX:66036973 | A | AATATAAT others(22): Show |
3 | a0001c0001t0001g0068 a0001c0001t0004g0006 a0001c0001t0004g0011 |
6 | HG00642.hp1 HG00735.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2942_55+2970dup others(29): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036973 | |||||||
| chrX:66036973 | A | C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0005g0035 others(1): Show |
4 | HG00639.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2971T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036973 | |||||||
| chrX:66036973 | A | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
4 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2971T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036973 | |||||||
| chrX:66036974 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2970T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036974 | |||||||
| chrX:66036977 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2967A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036977 | |||||||
| chrX:66036978 | A | ATT | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2965_55+2966ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036978 | |||||||
| chrX:66036979 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2965T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036979 | |||||||
| chrX:66036980 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2964A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036980 | |||||||
| chrX:66036985 | C | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2959G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036985 | |||||||
| chrX:66036985 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2959G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036985 | |||||||
| chrX:66036985 | CATATA | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0033 others(36): Show |
44 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.55+2954_55+2958del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036985 | |||||||
| chrX:66036991 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2953T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036991 | |||||||
| chrX:66036992 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2952A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036992 | |||||||
| chrX:66036992 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2952A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036992 | |||||||
| chrX:66036997 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2947A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036997 | |||||||
| chrX:66036999 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2945A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66036999 | |||||||
| chrX:66037001 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0002g0025 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+2943A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037001 | |||||||
| chrX:66037001 | TC | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2942delG | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037001 | |||||||
| chrX:66037002 | C | A | 32 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0039 others(29): Show |
33 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.55+2942G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037002 | |||||||
| chrX:66037002 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0002g0025 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+2942G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037002 | |||||||
| chrX:66037003 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2941T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037003 | |||||||
| chrX:66037007 | A | G | 8 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | HG00735.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+2937T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037007 | |||||||
| chrX:66037008 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2936T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037008 | |||||||
| chrX:66037009 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2935A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037009 | |||||||
| chrX:66037011 | TATC | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2930_55+2932del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037011 | |||||||
| chrX:66037014 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0002g0025 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.55+2930G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037014 | |||||||
| chrX:66037021 | TATA | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2920_55+2922del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037021 | |||||||
| chrX:66037030 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2914A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037030 | |||||||
| chrX:66037031 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2913T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037031 | |||||||
| chrX:66037032 | A | ATATACAT others(520): Show |
1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2911_55+2912ins others(527): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037032 | |||||||
| chrX:66037032 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2912T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037032 | |||||||
| chrX:66037034 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2910C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037034 | |||||||
| chrX:66037038 | T | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2906A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037038 | |||||||
| chrX:66037041 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2903T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037041 | |||||||
| chrX:66037043 | TATATC | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0066 |
3 | HG01192.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.55+2896_55+2900del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037043 | |||||||
| chrX:66037045 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2899A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037045 | |||||||
| chrX:66037047 | T | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0002g0025 |
3 | HG02572.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2897A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037047 | |||||||
| chrX:66037048 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2896G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037048 | |||||||
| chrX:66037048 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0002g0025 |
3 | HG02572.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2896G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037048 | |||||||
| chrX:66037049 | A | C | 1 | a0001c0001t0001g0051 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55+2895T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037049 | |||||||
| chrX:66037053 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2891T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037053 | |||||||
| chrX:66037054 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2890T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037054 | |||||||
| chrX:66037056 | A | AAT | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2887_55+2888ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037056 | |||||||
| chrX:66037061 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2883A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037061 | |||||||
| chrX:66037062 | T | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG02622.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2882A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037062 | |||||||
| chrX:66037063 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+2881T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037063 | |||||||
| chrX:66037064 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55+2880A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037064 | |||||||
| chrX:66037064 | T | TATAATAA others(570): Show |
2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2879_55+2880ins others(577): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037064 | |||||||
| chrX:66037070 | A | AT | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2873_55+2874ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037070 | |||||||
| chrX:66037075 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2869T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037075 | |||||||
| chrX:66037081 | T | A | 4 | a0001c0001t0001g0098 a0001c0001t0002g0025 a0001c0001t0005g0035 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2863A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037081 | |||||||
| chrX:66037081 | T | TTA | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2862_55+2863ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037081 | |||||||
| chrX:66037082 | C | T | 6 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0001g0149 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+2862G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037082 | |||||||
| chrX:66037090 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2854T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037090 | |||||||
| chrX:66037091 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2853A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037091 | |||||||
| chrX:66037093 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2851A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037093 | |||||||
| chrX:66037099 | A | ATAG | 3 | a0001c0001t0001g0098 a0001c0001t0005g0035 a0001c0001t0005g0036 |
3 | HG02615.hp1 HG02976.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.55+2844_55+2845ins others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037099 | |||||||
| chrX:66037100 | TA | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2843delT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037100 | |||||||
| chrX:66037110 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2834T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037110 | |||||||
| chrX:66037111 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2833A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037111 | |||||||
| chrX:66037118 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2826A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037118 | |||||||
| chrX:66037119 | A | ATAAT | 4 | a0001c0001t0001g0098 a0001c0001t0002g0025 a0001c0001t0005g0035 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2824_55+2825ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037119 | |||||||
| chrX:66037119 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2825T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037119 | |||||||
| chrX:66037121 | A | AATATATA others(716): Show |
1 | a0001c0001t0001g0125 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(723): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(753): Show |
1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(760): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(682): Show |
1 | a0001c0001t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(689): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(695): Show |
1 | a0001c0001t0002g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(702): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(797): Show |
1 | a0005c0006t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(804): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(653): Show |
2 | a0001c0001t0002g0026 a0001c0001t0002g0027 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(660): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(684): Show |
1 | a0001c0001t0002g0029 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(650): Show |
1 | a0001c0001t0002g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(657): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(684): Show |
1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(684): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0037 others(4): Show |
11 | HG01884.hp1 HG02257.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(718): Show |
1 | a0001c0001t0001g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(725): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(786): Show |
1 | a0001c0001t0001g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(793): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(781): Show |
1 | a0001c0001t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(788): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(752): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG00735.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(759): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(684): Show |
1 | a0001c0001t0001g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(684): Show |
2 | a0003c0005t0001g0134 a0003c0005t0001g0135 |
2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(684): Show |
3 | a0001c0001t0001g0121 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG03492.hp1 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(685): Show |
1 | a0001c0001t0001g0138 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(692): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(687): Show |
1 | a0001c0004t0001g0023 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(694): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(684): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG01496.hp2 HG01978.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(691): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(651): Show |
1 | a0001c0001t0002g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(658): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(585): Show |
1 | a0001c0001t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(592): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(582): Show |
1 | a0001c0001t0001g0113 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(589): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(608): Show |
1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(615): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(584): Show |
1 | a0001c0001t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(612): Show |
1 | a0001c0001t0001g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(619): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(554): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
6 | HG00438.hp1 HG00438.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(561): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(672): Show |
1 | a0002c0002t0001g0019 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(679): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(688): Show |
1 | a0002c0002t0001g0018 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(695): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(729): Show |
2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(736): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(669): Show |
1 | a0001c0001t0001g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(676): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(584): Show |
1 | a0001c0001t0001g0154 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(616): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0096 |
6 | NA18957.hp2 NA18960.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(623): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(620): Show |
1 | a0001c0001t0003g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(627): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(629): Show |
1 | a0001c0001t0001g0059 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(636): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(584): Show |
1 | a0001c0001t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(581): Show |
2 | a0001c0001t0001g0021 a0001c0001t0001g0103 |
3 | NA18971.hp1 NA18986.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(588): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(615): Show |
1 | a0001c0001t0001g0054 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(622): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(584): Show |
59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(56): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(618): Show |
5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0101 others(2): Show |
5 | HG01361.hp1 HG02074.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(625): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(621): Show |
1 | a0001c0001t0001g0057 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(628): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(609): Show |
1 | a0001c0001t0001g0117 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(616): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(581): Show |
1 | a0001c0001t0001g0005 | 3 | HG02155.hp2 NA18945.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(588): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(614): Show |
1 | a0001c0001t0001g0062 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(621): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(582): Show |
2 | a0001c0001t0001g0061 a0001c0001t0007g0060 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(589): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(582): Show |
1 | a0001c0001t0001g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(589): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(614): Show |
1 | a0001c0001t0003g0107 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(621): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(648): Show |
2 | a0001c0001t0003g0099 a0001c0001t0003g0100 |
2 | NA18999.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(655): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(584): Show |
1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(591): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(759): Show |
1 | a0001c0001t0001g0024 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.55+2822_55+2823ins others(766): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(620): Show |
1 | a0001c0001t0001g0051 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(627): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATATA others(604): Show |
1 | a0001c0001t0001g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(611): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | AATATTAT others(715): Show |
1 | a0001c0001t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2822_55+2823ins others(722): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037121 | A | T | 7 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
7 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2823T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037121 | |||||||
| chrX:66037123 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2821A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037123 | |||||||
| chrX:66037124 | AT | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2819delA | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037124 | |||||||
| chrX:66037125 | T | TATAATAT others(503): Show |
1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2818_55+2819ins others(510): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037125 | |||||||
| chrX:66037125 | T | TATATAAT others(549): Show |
1 | a0001c0001t0001g0106 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.55+2818_55+2819ins others(556): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037125 | |||||||
| chrX:66037125 | T | TATATAAT others(482): Show |
1 | a0001c0001t0001g0112 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55+2818_55+2819ins others(489): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037125 | |||||||
| chrX:66037125 | T | TATATAAT others(549): Show |
4 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0047 others(1): Show |
5 | HG03834.hp1 HG04228.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2818_55+2819ins others(556): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037125 | |||||||
| chrX:66037126 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2818A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037126 | |||||||
| chrX:66037128 | T | TA | 2 | a0001c0001t0001g0112 a0001c0001t0001g0120 |
2 | NA18906.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.55+2815dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037128 | |||||||
| chrX:66037129 | A | AG | 5 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0047 others(2): Show |
6 | HG01074.hp1 HG03834.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2814_55+2815ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037129 | |||||||
| chrX:66037131 | A | ACATT | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2812_55+2813ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037131 | |||||||
| chrX:66037131 | A | G | 4 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2813T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037131 | |||||||
| chrX:66037131 | A | T | 3 | a0001c0001t0001g0124 a0001c0001t0002g0029 a0001c0001t0002g0031 |
3 | HG01516.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.55+2813T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037131 | |||||||
| chrX:66037134 | A | ATATATAA others(118): Show |
3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2809_55+2810ins others(125): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037134 | |||||||
| chrX:66037135 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2809T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037135 | |||||||
| chrX:66037136 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2808A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037136 | |||||||
| chrX:66037136 | T | TA | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2807dupT | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037136 | |||||||
| chrX:66037137 | A | ATAATGTA others(68): Show |
1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2806_55+2807ins others(75): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037137 | |||||||
| chrX:66037139 | A | C | 3 | a0001c0001t0001g0127 a0001c0001t0002g0028 a0001c0001t0002g0030 |
3 | HG02922.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.55+2805T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037139 | |||||||
| chrX:66037152 | A | T | 7 | a0001c0001t0001g0124 a0001c0001t0002g0026 a0001c0001t0002g0027 others(4): Show |
7 | HG01516.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2792T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037152 | |||||||
| chrX:66037157 | T | C | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2787A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037157 | |||||||
| chrX:66037159 | T | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG00621.hp1 HG01361.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2785A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037159 | |||||||
| chrX:66037163 | A | ATAG | 2 | a0001c0001t0001g0112 a0001c0001t0001g0120 |
2 | NA18906.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.55+2780_55+2781ins others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037163 | |||||||
| chrX:66037165 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0027 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+2779T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037165 | |||||||
| chrX:66037165 | AATAAT | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2774_55+2778del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037165 | |||||||
| chrX:66037167 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2777A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037167 | |||||||
| chrX:66037173 | A | C | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0030 |
3 | HG01884.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.55+2771T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037173 | |||||||
| chrX:66037174 | A | ATG | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2769_55+2770ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037174 | |||||||
| chrX:66037179 | A | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2765T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037179 | |||||||
| chrX:66037180 | T | TATATAAT others(20): Show |
1 | a0001c0001t0001g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.55+2763_55+2764ins others(27): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037180 | |||||||
| chrX:66037186 | A | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0027 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+2758T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037186 | |||||||
| chrX:66037187 | T | TAATA | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2756_55+2757ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037187 | |||||||
| chrX:66037190 | A | G | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2754T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037190 | |||||||
| chrX:66037193 | A | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0022 others(56): Show |
66 | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.55+2751T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037193 | |||||||
| chrX:66037199 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0027 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.55+2745T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037199 | |||||||
| chrX:66037201 | T | C | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2743A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037201 | |||||||
| chrX:66037202 | A | AT | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2741_55+2742ins others(1): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037202 | |||||||
| chrX:66037207 | A | C | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0030 |
3 | HG01884.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.55+2737T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037207 | |||||||
| chrX:66037207 | A | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2737T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037207 | |||||||
| chrX:66037213 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2731T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037213 | |||||||
| chrX:66037214 | T | TAATA | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2729_55+2730ins others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037214 | |||||||
| chrX:66037216 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.55+2728A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037216 | |||||||
| chrX:66037217 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2727T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037217 | |||||||
| chrX:66037218 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2726A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037218 | |||||||
| chrX:66037219 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55+2725T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037219 | |||||||
| chrX:66037220 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.55+2724T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037220 | |||||||
| chrX:66037227 | T | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0106 others(5): Show |
9 | HG00733.hp1 HG01074.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+2717A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037227 | |||||||
| chrX:66037235 | TAATA | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+2705_55+2708del others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037235 | |||||||
| chrX:66037237 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2707T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037237 | |||||||
| chrX:66037241 | A | C | 2 | a0001c0001t0002g0026 a0001c0001t0002g0030 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.55+2703T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037241 | |||||||
| chrX:66037244 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.55+2700T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037244 | |||||||
| chrX:66037246 | A | ATATAATA others(137): Show |
1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2697_55+2698ins others(144): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037246 | |||||||
| chrX:66037250 | T | C | 15 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
17 | HG00733.hp2 HG01168.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.55+2694A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037250 | |||||||
| chrX:66037251 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2693T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037251 | |||||||
| chrX:66037253 | A | ATTATATT others(124): Show |
1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2690_55+2691ins others(131): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037253 | |||||||
| chrX:66037261 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55+2683A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037261 | |||||||
| chrX:66037264 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+2680A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037264 | |||||||
| chrX:66037264 | TATA | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.55+2677_55+2679del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037264 | |||||||
| chrX:66037267 | A | T | 1 | a0001c0001t0002g0029 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.55+2677T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037267 | |||||||
| chrX:66037267 | AATAAT | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0146 |
2 | HG01192.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.55+2672_55+2676del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037267 | |||||||
| chrX:66037272 | T | TAATATAA others(43): Show |
1 | a0001c0001t0001g0151 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.55+2671_55+2672ins others(50): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037272 | |||||||
| chrX:66037272 | T | TATAATAT others(22): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
7 | HG01081.hp2 HG01256.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+2643_55+2671dup others(29): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037272 | |||||||
| chrX:66037273 | A | AATATAAC others(14): Show |
2 | a0001c0001t0001g0153 a0001c0007t0001g0152 |
2 | HG00738.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2670_55+2671ins others(21): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037273 | |||||||
| chrX:66037273 | A | AATATAAT others(44): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2670_55+2671ins others(51): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037273 | |||||||
| chrX:66037275 | A | C | 1 | a0001c0001t0002g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.55+2669T>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037275 | |||||||
| chrX:66037285 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2659T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037285 | |||||||
| chrX:66037288 | A | T | 1 | a0001c0001t0001g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.55+2656T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037288 | |||||||
| chrX:66037295 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2649A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037295 | |||||||
| chrX:66037300 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+2644A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037300 | |||||||
| chrX:66037301 | A | AATAAT | 41 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(38): Show |
47 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.55+2638_55+2642dup others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037301 | |||||||
| chrX:66037301 | A | AATAATAT others(27): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG00280.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.55+2609_55+2642dup others(34): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037301 | |||||||
| chrX:66037301 | A | T | 2 | a0001c0001t0001g0122 a0001c0001t0002g0025 |
2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.55+2643T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037301 | |||||||
| chrX:66037309 | AAT | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0111 a0002c0002t0001g0018 others(1): Show |
7 | HG01167.hp1 HG01169.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2633_55+2634del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037309 | |||||||
| chrX:66037314 | A | AATATG | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2629_55+2630ins others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037314 | |||||||
| chrX:66037316 | A | ATAATAAT others(221): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.55+2627_55+2628ins others(228): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037316 | |||||||
| chrX:66037324 | T | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0111 |
3 | HG03834.hp1 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55+2620A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037324 | |||||||
| chrX:66037330 | A | ATT | 2 | a0001c0001t0001g0020 a0001c0001t0001g0111 |
3 | HG03834.hp1 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55+2613_55+2614ins others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037330 | |||||||
| chrX:66037330 | AATAAT | A | 1 | a0001c0001t0001g0021 | 2 | NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.55+2609_55+2613del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037330 | |||||||
| chrX:66037334 | A | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0111 |
3 | HG03834.hp1 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55+2610T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037334 | |||||||
| chrX:66037335 | T | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0111 |
3 | HG03834.hp1 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.55+2609A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | |||||||
| chrX:66037335 | T | TATAATAT others(22): Show |
1 | a0001c0001t0001g0112 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55+2580_55+2608dup others(29): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | |||||||
| chrX:66037335 | T | TATAATAT others(85): Show |
1 | a0001c0001t0001g0113 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.55+2608_55+2609ins others(92): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | |||||||
| chrX:66037335 | T | TATAATAT others(46): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG01952.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.55+2608_55+2609ins others(53): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | |||||||
| chrX:66037335 | T | TATAATAT others(263): Show |
2 | a0001c0001t0001g0153 a0001c0007t0001g0152 |
2 | HG00738.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2608_55+2609ins others(270): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | |||||||
| chrX:66037335 | T | TATAATAT others(288): Show |
1 | a0001c0001t0001g0151 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.55+2608_55+2609ins others(295): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037335 | |||||||
| chrX:66037351 | A | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2593T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037351 | |||||||
| chrX:66037362 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0042 |
3 | NA18946.hp2 NA18973.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.55+2582T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037362 | |||||||
| chrX:66037385 | A | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2559T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037385 | |||||||
| chrX:66037396 | G | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(47): Show |
56 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.55+2548C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037396 | |||||||
| chrX:66037423 | C | CATATAAT others(21): Show |
1 | a0001c0001t0001g0012 | 2 | HG02071.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.55+2493_55+2520dup others(28): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037423 | |||||||
| chrX:66037423 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2521G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037423 | |||||||
| chrX:66037443 | A | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2501T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037443 | |||||||
| chrX:66037451 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2493A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037451 | |||||||
| chrX:66037488 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2456G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037488 | |||||||
| chrX:66037504 | T | TAATACAA others(7): Show |
1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2439_55+2440ins others(14): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037504 | |||||||
| chrX:66037507 | TATA | T | 4 | a0001c0001t0001g0121 a0001c0001t0004g0011 a0001c0001t0005g0035 others(1): Show |
5 | HG01433.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+2434_55+2436del others(3): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037507 | |||||||
| chrX:66037511 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2433T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037511 | |||||||
| chrX:66037512 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2432A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037512 | |||||||
| chrX:66037520 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2424A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037520 | |||||||
| chrX:66037538 | ATATAT | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0003g0116 others(1): Show |
4 | HG00621.hp1 HG00738.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2401_55+2405del others(5): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037538 | |||||||
| chrX:66037541 | T | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.55+2403A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037541 | |||||||
| chrX:66037557 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.55+2387T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037557 | |||||||
| chrX:66037570 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2374A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037570 | |||||||
| chrX:66037573 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2371A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037573 | |||||||
| chrX:66037575 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2369A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037575 | |||||||
| chrX:66037576 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2368T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037576 | |||||||
| chrX:66037577 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2367A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037577 | |||||||
| chrX:66037578 | T | G | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2366A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037578 | |||||||
| chrX:66037580 | T | G | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2364A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037580 | |||||||
| chrX:66037582 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2362A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037582 | |||||||
| chrX:66037583 | T | G | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2361A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037583 | |||||||
| chrX:66037585 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.55+2359G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037585 | |||||||
| chrX:66037643 | T | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0007t0001g0152 |
3 | HG00738.hp1 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55+2301A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037643 | |||||||
| chrX:66037757 | C | CGTATATA others(16): Show |
4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG00099.hp1 HG01081.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2164_55+2186dup others(23): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037757 | |||||||
| chrX:66037757 | C | CGTATATA others(39): Show |
32 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0033 others(29): Show |
37 | HG00733.hp2 HG00735.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.55+2141_55+2186dup others(46): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037757 | |||||||
| chrX:66037757 | C | CGTATATA others(62): Show |
4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG01255.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2186_55+2187ins others(69): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037757 | |||||||
| chrX:66037805 | T | C | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+2139A>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037805 | |||||||
| chrX:66037808 | A | ATATACTT others(40): Show |
1 | a0001c0001t0002g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55+2135_55+2136ins others(47): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037808 | |||||||
| chrX:66037813 | C | CTTATTGC others(5): Show |
1 | a0001c0001t0002g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.55+2130_55+2131ins others(12): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037813 | |||||||
| chrX:66037818 | T | TATATACA others(3): Show |
1 | a0001c0001t0002g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.55+2125_55+2126ins others(10): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037818 | |||||||
| chrX:66037852 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.55+2092T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037852 | |||||||
| chrX:66037998 | A | G | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+1946T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66037998 | |||||||
| chrX:66038174 | G | A | 2 | a0001c0001t0003g0144 a0001c0001t0003g0145 |
2 | NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.55+1770C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038174 | |||||||
| chrX:66038202 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.55+1742A>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038202 | |||||||
| chrX:66038373 | G | C | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+1571C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038373 | |||||||
| chrX:66038426 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.55+1518C>G | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038426 | |||||||
| chrX:66038479 | TCTCA | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 |
3 | HG01884.hp2 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.55+1461_55+1464del others(4): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038479 | |||||||
| chrX:66038481 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.55+1463A>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038481 | |||||||
| chrX:66038481 | T | TCA | 4 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0089 others(1): Show |
5 | HG00438.hp1 HG02135.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1461_55+1462dup others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038481 | |||||||
| chrX:66038481 | TCA | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(41): Show |
50 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.55+1461_55+1462del others(2): Show |
VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038481 | |||||||
| chrX:66038485 | A | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+1459T>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038485 | |||||||
| chrX:66038528 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.55+1416G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038528 | |||||||
| chrX:66038847 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.55+1097G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038847 | |||||||
| chrX:66038847 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.55+1097G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66038847 | |||||||
| chrX:66039040 | C | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.55+904G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039040 | |||||||
| chrX:66039049 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.55+895T>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039049 | |||||||
| chrX:66039153 | C | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+791G>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039153 | |||||||
| chrX:66039188 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55+756G>A | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039188 | |||||||
| chrX:66039251 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.55+693C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039251 | |||||||
| chrX:66039541 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.55+403G>C | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039541 | |||||||
| chrX:66039648 | G | A | 6 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(3): Show |
6 | HG01516.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+296C>T | VSIG4 | ENSG00000155659.15 | transcript | ENST00000374737.9 | protein_coding | 1/7 | chrX | 66039648 |