Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79868 |
| ensemblid | ENSG00000101901.13 |
| hgncid | 30881 |
| symbol | ALG13 |
| name | ALG13 UDP-N-acetylglucosaminyltransferase subunit |
| refseq_nuc | NM_001099922.3 |
| refseq_prot | NP_001093392.1 |
| ensembl_nuc | ENST00000394780.8 |
| ensembl_prot | ENSP00000378260.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 111681170 |
| end | 111760649 |
| strand | + |
| ver | v1.2 |
| region | chrX:111681170-111760649 |
| region5000 | chrX:111676170-111765649 |
| regionname0 | ALG13_chrX_111681170_111760649 |
| regionname5000 | ALG13_chrX_111676170_111765649 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1137 | 165 | 61 | 21 | 61 | 5 | 15 | 46 | ALG13_chrX_111676170_111765649 | ALG13 | MKCVF others(1132): Show |
chrX | 111676170 | 111765649 |
| a0002 | 0/0 | 1138 | 15 | 6 | 1 | 7 | 0 | 1 | 5 | ALG13_chrX_111676170_111765649 | ALG13 | MKCVF others(1133): Show |
chrX | 111676170 | 111765649 |
| a0003 | 0/0 | 1136 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | MKCVF others(1131): Show |
chrX | 111676170 | 111765649 |
| a0004 | 0/0 | 1139 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | MKCVF others(1134): Show |
chrX | 111676170 | 111765649 |
| a0005 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | MKCVF others(1132): Show |
chrX | 111676170 | 111765649 |
| a0006 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | MKCVF others(1132): Show |
chrX | 111676170 | 111765649 |
| a0007 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | MKCVF others(1132): Show |
chrX | 111676170 | 111765649 |
| a0008 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | MKCVF others(1132): Show |
chrX | 111676170 | 111765649 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3411 | 140 | 39 | 20 | 60 | 5 | 15 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 | ||
| a0001c0002 | 0/0 | 3411 | 21 | 21 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 | ||
| a0001c0006 | 0/1 | 3411 | 2 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 | ||
| a0001c0010 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 | ||
| a0001c0013 | 0/0 | 3411 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 | ||
| a0002c0003 | 0/0 | 3414 | 11 | 2 | 1 | 7 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3409): Show |
chrX | 111676170 | 111765649 | ||
| a0002c0005 | 0/0 | 3414 | 3 | 3 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3409): Show |
chrX | 111676170 | 111765649 | ||
| a0002c0008 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3409): Show |
chrX | 111676170 | 111765649 | ||
| a0003c0004 | 0/0 | 3408 | 4 | 4 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3403): Show |
chrX | 111676170 | 111765649 | ||
| a0004c0007 | 0/0 | 3417 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3412): Show |
chrX | 111676170 | 111765649 | ||
| a0004c0009 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3412): Show |
chrX | 111676170 | 111765649 | ||
| a0005c0012 | 0/0 | 3411 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 | ||
| a0006c0011 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 | ||
| a0007c0015 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 | ||
| a0008c0014 | 0/0 | 3411 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | ATGAA others(3406): Show |
chrX | 111676170 | 111765649 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4113 | 139 | 39 | 20 | 59 | 5 | 15 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0001c0001t0002 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0001c0002t0001 | 0/0 | 4113 | 21 | 21 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0001c0006t0001 | 0/1 | 4113 | 2 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0001c0010t0001 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0001c0013t0001 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0002c0003t0001 | 0/0 | 4116 | 11 | 2 | 1 | 7 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4111): Show |
chrX | 111676170 | 111765649 |
| a0002c0005t0001 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4111): Show |
chrX | 111676170 | 111765649 |
| a0002c0008t0001 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4111): Show |
chrX | 111676170 | 111765649 |
| a0003c0004t0001 | 0/0 | 4110 | 4 | 4 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4105): Show |
chrX | 111676170 | 111765649 |
| a0004c0007t0001 | 0/0 | 4119 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4114): Show |
chrX | 111676170 | 111765649 |
| a0004c0009t0001 | 0/0 | 4119 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4114): Show |
chrX | 111676170 | 111765649 |
| a0005c0012t0001 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0006c0011t0001 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0007c0015t0001 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| a0008c0014t0001 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | AGTTG others(4108): Show |
chrX | 111676170 | 111765649 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0006t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0006t0001g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0001c0013t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0005t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0002c0008t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0003c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0003c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0003c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0003c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0004c0007t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0004c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0004c0009t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0005c0012t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0006c0011t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0007c0015t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| a0008c0014t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG00558 | hp2 | a0001 | c0010 | t0001 | g0096 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0149 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01358 | hp1 | a0001 | c0006 | t0001 | g0154 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01496 | hp2 | a0005 | c0012 | t0001 | g0101 | AMR | CLM | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02027 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0174 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02257 | hp1 | a0002 | c0005 | t0001 | g0074 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02258 | hp1 | a0004 | c0009 | t0001 | g0043 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02897 | hp2 | a0001 | c0013 | t0001 | g0042 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0065 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02976 | hp1 | a0003 | c0004 | t0001 | g0009 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02976 | hp2 | a0002 | c0005 | t0001 | g0022 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03139 | hp1 | a0002 | c0008 | t0001 | g0047 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0063 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03486 | hp1 | a0003 | c0004 | t0001 | g0067 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03579 | hp1 | a0002 | c0005 | t0001 | g0025 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0179 | SAS | BEB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0084 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18995 | hp1 | a0006 | c0011 | t0001 | g0165 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0052 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19063 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0151 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19068 | hp1 | a0007 | c0015 | t0001 | g0129 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19086 | hp1 | a0008 | c0014 | t0001 | g0145 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ASW | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG03471 | hp1 | a0003 | c0004 | t0001 | g0066 | AFR | MSL | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | USA | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| HG06807 | hp2 | a0004 | c0007 | t0001 | g0016 | AFR | USA | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA20300 | hp1 | a0004 | c0007 | t0001 | g0017 | AFR | USA | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | USA | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| homoSapiens | chm13v2 | a0001 | c0006 | t0001 | g0177 | REF | REF | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0089 | REF | REF | ALG13_chrX_111676170_111765649 | ALG13 | chrX | 111676170 | 111765649 |
| 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:111711720 | C | T | 1 | a0008 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.880C>T | p.Pro294Ser | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 6/27 | 929/4113 | 880/3414 | 294/1137 | chrX | 111711720 | |||
| chrX:111712521 | T | C | 1 | a0007 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.923T>C | p.Leu308Pro | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 7/27 | 972/4113 | 923/3414 | 308/1137 | chrX | 111712521 | |||
| chrX:111721664 | A | G | 1 | a0005 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1388A>G | p.Glu463Gly | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 12/27 | 1437/4113 | 1388/3414 | 463/1137 | chrX | 111721664 | |||
| chrX:111744725 | T | TACC | 2 | a0001 a0002 |
16 | HG00558.hp2 HG01099.hp1 HG02027.hp1 others(13): Show |
disruptive_inframe_insertion | MODERATE | c.2796_2798dupACC | p.Pro933dup | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2848/4113 | 2799/3414 | 933/1137 | INFO_REALIGN_3_PRIME | chrX | 111744725 | ||
| chrX:111744725 | T | TACCACC | 1 | a0004 | 3 | HG02258.hp1 HG06807.hp2 NA20300.hp1 |
disruptive_inframe_insertion | MODERATE | c.2793_2798dupACCACC | p.Pro932_Pro933dup | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2848/4113 | 2799/3414 | 933/1137 | INFO_REALIGN_3_PRIME | chrX | 111744725 | ||
| chrX:111744768 | ACCT | A | 2 | a0001 a0003 |
5 | HG00558.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
conservative_inframe_deletion | MODERATE | c.2833_2835delCCT | p.Pro945del | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2882/4113 | 2833/3414 | 945/1137 | INFO_REALIGN_3_PRIME | chrX | 111744768 | ||
| chrX:111744806 | C | T | 1 | a0006 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.2834C>T | p.Pro945Leu | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2883/4113 | 2834/3414 | 945/1137 | chrX | 111744806 |
| 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:111685054 | C | T | 1 | a0007c0015 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.334C>T | p.Leu112Leu | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/27 | 383/4113 | 334/3414 | 112/1137 | chrX | 111685054 | |||
| chrX:111718176 | G | A | 1 | a0002c0008 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1152G>A | p.Ala384Ala | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/27 | 1201/4113 | 1152/3414 | 384/1137 | chrX | 111718176 | |||
| chrX:111720110 | T | C | 1 | a0001c0006 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1266T>C | p.Gly422Gly | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/27 | 1315/4113 | 1266/3414 | 422/1137 | chrX | 111720110 | |||
| chrX:111720137 | A | G | 5 | a0001c0002 a0001c0013 a0002c0005 others(2): Show |
28 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
synonymous_variant | LOW | c.1293A>G | p.Pro431Pro | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/27 | 1342/4113 | 1293/3414 | 431/1137 | chrX | 111720137 | |||
| chrX:111744771 | T | A | 1 | a0001c0001 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.2799T>A | p.Pro933Pro | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/27 | 2848/4113 | 2799/3414 | 933/1137 | chrX | 111744771 | |||
| chrX:111757653 | A | G | 1 | a0001c0013 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.3039A>G | p.Val1013Val | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/27 | 3088/4113 | 3039/3414 | 1013/1137 | chrX | 111757653 |
| 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:111760578 | C | T | 1 | a0001c0001t0002 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 27/27 | 579 | chrX | 111760578 |
| 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:111681395 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.81+96C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681395 | |||||||
| chrX:111681562 | G | C | 1 | a0001c0001t0001g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.81+263G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681562 | |||||||
| chrX:111681572 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81+273G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681572 | |||||||
| chrX:111681630 | G | A | 1 | a0003c0004t0001g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.81+331G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681630 | |||||||
| chrX:111681644 | C | T | 1 | a0001c0002t0001g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81+345C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681644 | |||||||
| chrX:111681757 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01934.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.82-375G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | chrX | 111681757 | |||||||
| chrX:111681980 | A | ATACTT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.82-150_82-149insCT others(3): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chrX | 111681980 | ||||||
| chrX:111682362 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.244+68C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111682362 | |||||||
| chrX:111682994 | C | T | 1 | a0002c0005t0001g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.244+700C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111682994 | |||||||
| chrX:111683326 | A | AT | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0068 others(11): Show |
14 | HG02257.hp2 HG02818.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+1051dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111683326 | ||||||
| chrX:111683326 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244+1032A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683326 | |||||||
| chrX:111683326 | AT | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.244+1051delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chrX | 111683326 | ||||||
| chrX:111683394 | A | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(8): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+1100A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683394 | |||||||
| chrX:111683398 | C | T | 4 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0059 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+1104C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683398 | |||||||
| chrX:111683856 | G | A | 3 | a0001c0002t0001g0018 a0004c0007t0001g0016 a0004c0007t0001g0017 |
3 | HG01891.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.245-1109G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111683856 | |||||||
| chrX:111684039 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.245-926C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111684039 | |||||||
| chrX:111684096 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
5 | NA18943.hp1 NA18959.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-869G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 2/26 | chrX | 111684096 | |||||||
| chrX:111685341 | G | GT | 10 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
10 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.383+239dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111685341 | ||||||
| chrX:111685364 | G | A | 1 | a0001c0002t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.383+261G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111685364 | |||||||
| chrX:111685923 | A | G | 1 | a0002c0005t0001g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.383+820A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111685923 | |||||||
| chrX:111685934 | G | A | 22 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0020 others(19): Show |
23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.383+831G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111685934 | |||||||
| chrX:111686132 | A | G | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.383+1029A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686132 | |||||||
| chrX:111686164 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.383+1061C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686164 | |||||||
| chrX:111686232 | G | A | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+1129G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686232 | |||||||
| chrX:111686689 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.383+1586A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686689 | |||||||
| chrX:111686727 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.383+1624A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686727 | |||||||
| chrX:111686831 | A | T | 1 | a0002c0003t0001g0079 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.383+1728A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111686831 | |||||||
| chrX:111687023 | T | C | 1 | a0001c0002t0001g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.383+1920T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687023 | |||||||
| chrX:111687102 | G | A | 26 | a0001c0001t0001g0035 a0001c0002t0001g0002 a0001c0002t0001g0018 others(23): Show |
27 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.383+1999G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687102 | |||||||
| chrX:111687209 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(7): Show |
10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.383+2106T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687209 | |||||||
| chrX:111687309 | A | G | 1 | a0002c0003t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.383+2206A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687309 | |||||||
| chrX:111687612 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.383+2509T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687612 | |||||||
| chrX:111687763 | T | C | 1 | a0001c0001t0001g0010 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383+2660T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111687763 | |||||||
| chrX:111688035 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.383+2932C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688035 | |||||||
| chrX:111688420 | A | G | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.383+3317A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688420 | |||||||
| chrX:111688566 | CT | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+3472delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111688566 | ||||||
| chrX:111688580 | A | AACAT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.383+3481_383+3484d others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111688580 | ||||||
| chrX:111688632 | G | A | 2 | a0004c0007t0001g0016 a0004c0007t0001g0017 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.383+3529G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688632 | |||||||
| chrX:111688684 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+3581A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688684 | |||||||
| chrX:111688862 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.383+3759A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688862 | |||||||
| chrX:111688988 | A | G | 23 | a0001c0001t0001g0035 a0001c0002t0001g0002 a0001c0002t0001g0018 others(20): Show |
24 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+3885A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111688988 | |||||||
| chrX:111689114 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.383+4011G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689114 | |||||||
| chrX:111689303 | T | G | 3 | a0001c0002t0001g0018 a0004c0007t0001g0016 a0004c0007t0001g0017 |
3 | HG01891.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.383+4200T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689303 | |||||||
| chrX:111689315 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.383+4212C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689315 | |||||||
| chrX:111689561 | G | C | 23 | a0001c0001t0001g0035 a0001c0002t0001g0002 a0001c0002t0001g0018 others(20): Show |
24 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+4458G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689561 | |||||||
| chrX:111689926 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01884.hp1 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.383+4823G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111689926 | |||||||
| chrX:111690333 | G | A | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+5230G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690333 | |||||||
| chrX:111690344 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.383+5241C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690344 | |||||||
| chrX:111690453 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.383+5350T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690453 | |||||||
| chrX:111690631 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.383+5528T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690631 | |||||||
| chrX:111690646 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.383+5543G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111690646 | |||||||
| chrX:111690798 | G | GAC | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.383+5696_383+5697i others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111690798 | ||||||
| chrX:111691000 | G | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0002c0003t0001g0084 others(1): Show |
4 | HG02027.hp1 NA18967.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+5897G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691000 | |||||||
| chrX:111691027 | C | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
188 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.383+5924C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691027 | |||||||
| chrX:111691048 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01884.hp1 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.383+5945A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691048 | |||||||
| chrX:111691376 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.383+6273C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691376 | |||||||
| chrX:111691739 | G | GGTATGCT others(1): Show |
3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02451.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.383+6638_383+6645d others(10): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111691739 | ||||||
| chrX:111691859 | G | A | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383+6756G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691859 | |||||||
| chrX:111691894 | C | A | 1 | a0001c0002t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383+6791C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691894 | |||||||
| chrX:111691905 | G | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.383+6802G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111691905 | |||||||
| chrX:111692031 | A | G | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383+6928A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111692031 | |||||||
| chrX:111692801 | A | AT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+7708dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111692801 | ||||||
| chrX:111692863 | A | C | 28 | a0001c0001t0001g0035 a0001c0002t0001g0002 a0001c0002t0001g0018 others(25): Show |
29 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.383+7760A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111692863 | |||||||
| chrX:111693130 | C | T | 25 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0019 others(22): Show |
26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.383+8027C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693130 | |||||||
| chrX:111693164 | CT | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG00558.hp1 HG00642.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+8083delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111693164 | ||||||
| chrX:111693260 | A | AT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
7 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+8171dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111693260 | ||||||
| chrX:111693263 | T | TA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+8160_383+8161i others(3): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693263 | |||||||
| chrX:111693264 | T | A | 25 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0019 others(22): Show |
26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.383+8161T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693264 | |||||||
| chrX:111693387 | A | C | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383+8284A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693387 | |||||||
| chrX:111693429 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0162 others(7): Show |
12 | NA18952.hp1 NA18965.hp1 NA18966.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+8326A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693429 | |||||||
| chrX:111693899 | G | A | 22 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0020 others(19): Show |
23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.383+8796G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111693899 | |||||||
| chrX:111694051 | A | AT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(20): Show |
24 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+8958dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111694051 | ||||||
| chrX:111694055 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.383+8952T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111694055 | |||||||
| chrX:111694075 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.383+8972G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111694075 | |||||||
| chrX:111694530 | A | G | 20 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.383+9427A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111694530 | |||||||
| chrX:111695006 | T | C | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383+9903T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695006 | |||||||
| chrX:111695164 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.383+10061G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695164 | |||||||
| chrX:111695251 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+10148C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695251 | |||||||
| chrX:111695433 | T | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
75 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(72): Show |
intron_variant | MODIFIER | c.383+10330T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695433 | |||||||
| chrX:111695535 | A | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG01069.hp1 HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.383+10432A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695535 | |||||||
| chrX:111695555 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
188 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.383+10452G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695555 | |||||||
| chrX:111695695 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18990.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.383+10592C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695695 | |||||||
| chrX:111695961 | G | A | 22 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0020 others(19): Show |
23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.383+10858G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111695961 | |||||||
| chrX:111696068 | G | T | 1 | a0001c0002t0001g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383+10965G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696068 | |||||||
| chrX:111696149 | A | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+11046A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696149 | |||||||
| chrX:111696176 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.383+11073A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696176 | |||||||
| chrX:111696582 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.384-11445G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696582 | |||||||
| chrX:111696587 | G | A | 1 | a0001c0010t0001g0096 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.384-11440G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696587 | |||||||
| chrX:111696916 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.384-11111G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111696916 | |||||||
| chrX:111696982 | C | CT | 35 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(32): Show |
36 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.384-11024dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111696982 | ||||||
| chrX:111696982 | CT | C | 29 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(26): Show |
30 | HG01167.hp1 HG01256.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.384-11024delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111696982 | ||||||
| chrX:111697929 | A | G | 1 | a0001c0002t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.384-10098A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111697929 | |||||||
| chrX:111698499 | C | T | 2 | a0001c0001t0001g0100 a0005c0012t0001g0101 |
2 | HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.384-9528C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698499 | |||||||
| chrX:111698627 | C | G | 1 | a0001c0006t0001g0154 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.384-9400C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698627 | |||||||
| chrX:111698682 | A | G | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-9345A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698682 | |||||||
| chrX:111698695 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-9332G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698695 | |||||||
| chrX:111698914 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-9113A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111698914 | |||||||
| chrX:111699047 | A | G | 20 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.384-8980A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111699047 | |||||||
| chrX:111699187 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(68): Show |
73 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.384-8840T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111699187 | |||||||
| chrX:111699894 | AT | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
7 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-8122delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111699894 | ||||||
| chrX:111699905 | TC | T | 4 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0059 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-8121delC | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111699905 | |||||||
| chrX:111699906 | C | T | 18 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(15): Show |
18 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.384-8121C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111699906 | |||||||
| chrX:111700038 | G | GT | 44 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(41): Show |
44 | HG00621.hp1 HG01099.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.384-7973dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700038 | ||||||
| chrX:111700038 | GT | G | 10 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0102 others(7): Show |
10 | HG01074.hp1 HG01106.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.384-7973delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700038 | ||||||
| chrX:111700191 | G | A | 27 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0019 others(24): Show |
28 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.384-7836G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111700191 | |||||||
| chrX:111700202 | A | G | 1 | a0001c0002t0001g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.384-7825A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111700202 | |||||||
| chrX:111700494 | CT | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 |
4 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-7532delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111700494 | |||||||
| chrX:111700677 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02083.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.384-7350A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111700677 | |||||||
| chrX:111700751 | A | AT | 34 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0049 others(31): Show |
35 | HG01106.hp1 HG01891.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.384-7255dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700751 | ||||||
| chrX:111700751 | A | ATT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.384-7256_384-7255d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111700751 | ||||||
| chrX:111701557 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.384-6470C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111701557 | |||||||
| chrX:111701895 | T | A | 1 | a0001c0002t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.384-6132T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111701895 | |||||||
| chrX:111702224 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.384-5803T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702224 | |||||||
| chrX:111702660 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.384-5367A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702660 | |||||||
| chrX:111702731 | A | G | 11 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.384-5296A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702731 | |||||||
| chrX:111702780 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-5247T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702780 | |||||||
| chrX:111702827 | C | A | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.384-5200C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111702827 | |||||||
| chrX:111703152 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-4875T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111703152 | |||||||
| chrX:111703185 | G | GTCA | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(7): Show |
10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.384-4813_384-4811d others(5): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111703185 | ||||||
| chrX:111703185 | GTCATCA | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 |
4 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-4816_384-4811d others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111703185 | ||||||
| chrX:111703472 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.384-4555C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111703472 | |||||||
| chrX:111703758 | A | G | 4 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0059 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-4269A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111703758 | |||||||
| chrX:111704381 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
188 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.384-3646T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704381 | |||||||
| chrX:111704399 | T | C | 1 | a0001c0002t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.384-3628T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704399 | |||||||
| chrX:111704557 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.384-3470T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704557 | |||||||
| chrX:111704883 | T | G | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.384-3144T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704883 | |||||||
| chrX:111704954 | A | G | 20 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.384-3073A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111704954 | |||||||
| chrX:111705181 | A | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-2846A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111705181 | |||||||
| chrX:111705563 | G | C | 1 | a0002c0003t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.384-2464G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111705563 | |||||||
| chrX:111705632 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.384-2395T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111705632 | |||||||
| chrX:111705642 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.384-2385A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111705642 | |||||||
| chrX:111706059 | C | CT | 11 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(8): Show |
12 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.384-1955dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chrX | 111706059 | ||||||
| chrX:111706140 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.384-1887C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111706140 | |||||||
| chrX:111707378 | G | A | 4 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0032 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-649G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111707378 | |||||||
| chrX:111707428 | T | C | 1 | a0001c0013t0001g0042 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.384-599T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111707428 | |||||||
| chrX:111707814 | C | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.384-213C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111707814 | |||||||
| chrX:111707883 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.384-144C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 3/26 | chrX | 111707883 | |||||||
| chrX:111708780 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.751-185A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 4/26 | chrX | 111708780 | |||||||
| chrX:111709163 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG02257.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+115T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111709163 | |||||||
| chrX:111709242 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(6): Show |
9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.834+194A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111709242 | |||||||
| chrX:111709685 | C | CT | 26 | a0001c0001t0001g0064 a0001c0001t0001g0095 a0001c0001t0001g0105 others(23): Show |
27 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.834+651dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chrX | 111709685 | ||||||
| chrX:111709814 | A | G | 1 | a0002c0003t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.834+766A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111709814 | |||||||
| chrX:111710027 | CT | C | 21 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(18): Show |
21 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.834+992delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chrX | 111710027 | ||||||
| chrX:111710122 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.834+1074G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710122 | |||||||
| chrX:111710179 | C | T | 1 | a0002c0005t0001g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.834+1131C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710179 | |||||||
| chrX:111710189 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.834+1141C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710189 | |||||||
| chrX:111710301 | G | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18966.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.834+1253G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710301 | |||||||
| chrX:111710727 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.835-948T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710727 | |||||||
| chrX:111710904 | C | T | 1 | a0004c0009t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.835-771C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710904 | |||||||
| chrX:111710918 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.835-757C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710918 | |||||||
| chrX:111710977 | G | A | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-698G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111710977 | |||||||
| chrX:111711307 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-368C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111711307 | |||||||
| chrX:111711403 | A | G | 1 | a0001c0010t0001g0096 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.835-272A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111711403 | |||||||
| chrX:111711411 | T | G | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.835-264T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111711411 | |||||||
| chrX:111711653 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(55): Show |
60 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.835-22T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 5/26 | chrX | 111711653 | |||||||
| chrX:111712880 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.933-345T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 7/26 | chrX | 111712880 | |||||||
| chrX:111713016 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.933-209A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 7/26 | chrX | 111713016 | |||||||
| chrX:111713738 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1005+441C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111713738 | |||||||
| chrX:111713892 | G | A | 20 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1005+595G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111713892 | |||||||
| chrX:111713899 | G | C | 2 | a0001c0001t0001g0100 a0005c0012t0001g0101 |
2 | HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1005+602G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111713899 | |||||||
| chrX:111714032 | G | T | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+735G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714032 | |||||||
| chrX:111714033 | A | T | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+736A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714033 | |||||||
| chrX:111714049 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1005+752G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714049 | |||||||
| chrX:111714680 | A | C | 1 | a0001c0002t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1005+1383A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714680 | |||||||
| chrX:111714898 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1005+1601T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111714898 | |||||||
| chrX:111715602 | C | T | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1006-2244C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111715602 | |||||||
| chrX:111715649 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1006-2197C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111715649 | |||||||
| chrX:111715696 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1006-2150C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111715696 | |||||||
| chrX:111715753 | A | C | 1 | a0002c0003t0001g0087 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1006-2093A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111715753 | |||||||
| chrX:111716076 | A | G | 2 | a0004c0007t0001g0016 a0004c0007t0001g0017 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1006-1770A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111716076 | |||||||
| chrX:111716154 | C | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1006-1692C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111716154 | |||||||
| chrX:111716597 | TAACTTA | T | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-1243_1006-123 others(10): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chrX | 111716597 | ||||||
| chrX:111716672 | A | G | 17 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0020 others(14): Show |
18 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1006-1174A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111716672 | |||||||
| chrX:111717361 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1006-485C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717361 | |||||||
| chrX:111717541 | C | CT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
17 | HG00642.hp1 HG00673.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-286dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chrX | 111717541 | ||||||
| chrX:111717679 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1006-167G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717679 | |||||||
| chrX:111717726 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1006-120A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717726 | |||||||
| chrX:111717732 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1006-114T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717732 | |||||||
| chrX:111717749 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-97A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 8/26 | chrX | 111717749 | |||||||
| chrX:111718057 | A | G | 1 | a0001c0013t0001g0042 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1088-55A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 9/26 | chrX | 111718057 | |||||||
| chrX:111718385 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(6): Show |
9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250+111C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111718385 | |||||||
| chrX:111718425 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1250+151A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111718425 | |||||||
| chrX:111718590 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1250+316C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111718590 | |||||||
| chrX:111718623 | G | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0002c0003t0001g0084 others(1): Show |
4 | HG02027.hp1 NA18967.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+349G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111718623 | |||||||
| chrX:111719025 | C | CT | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0134 others(13): Show |
16 | HG00609.hp1 HG00673.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1250+770dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chrX | 111719025 | ||||||
| chrX:111719025 | CT | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
47 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1250+770delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chrX | 111719025 | ||||||
| chrX:111719025 | CTT | C | 25 | a0001c0001t0001g0038 a0001c0002t0001g0002 a0001c0002t0001g0018 others(22): Show |
26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1250+769_1250+770d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chrX | 111719025 | ||||||
| chrX:111719657 | G | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
70 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.1251-438G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111719657 | |||||||
| chrX:111720008 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1251-87C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 10/26 | chrX | 111720008 | |||||||
| chrX:111720217 | G | A | 1 | a0001c0002t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1326+47G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | chrX | 111720217 | |||||||
| chrX:111720824 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1326+654G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | chrX | 111720824 | |||||||
| chrX:111720919 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1327-684G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | chrX | 111720919 | |||||||
| chrX:111721056 | G | GT | 5 | a0001c0001t0001g0099 a0001c0001t0001g0133 a0001c0001t0001g0148 others(2): Show |
5 | HG01256.hp1 NA19005.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-533dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721056 | ||||||
| chrX:111721071 | A | AAGAAGGA others(25): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(24): Show |
29 | HG01261.hp1 HG01433.hp1 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1327-73_1327-42dup others(32): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(57): Show |
31 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
32 | HG00621.hp1 HG01167.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1327-105_1327-42du others(65): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(89): Show |
25 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0040 others(22): Show |
25 | HG01069.hp1 HG01099.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1327-137_1327-42du others(97): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(121): Show |
9 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0044 others(6): Show |
9 | HG01255.hp1 HG01928.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327-169_1327-42du others(129): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(153): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0035 others(4): Show |
8 | HG00609.hp1 HG02622.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1327-201_1327-42du others(161): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(185): Show |
5 | a0001c0001t0001g0037 a0001c0001t0001g0061 a0001c0001t0001g0069 others(2): Show |
5 | HG01243.hp1 HG02897.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-233_1327-42du others(193): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(217): Show |
9 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0056 others(6): Show |
9 | HG00673.hp1 HG01106.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327-265_1327-42du others(225): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(249): Show |
7 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0055 others(4): Show |
8 | HG01109.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1327-297_1327-42du others(257): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(281): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1327-329_1327-42du others(289): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(313): Show |
7 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG01891.hp1 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1327-361_1327-42du others(321): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(345): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0002t0001g0019 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1327-393_1327-42du others(353): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(377): Show |
3 | a0001c0001t0001g0015 a0001c0002t0001g0020 a0004c0007t0001g0017 |
3 | HG02615.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1327-425_1327-42du others(385): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(409): Show |
5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1327-457_1327-42du others(417): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(441): Show |
4 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0059 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-489_1327-42du others(449): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(473): Show |
2 | a0001c0002t0001g0018 a0002c0005t0001g0022 |
2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1327-521_1327-42du others(481): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(505): Show |
3 | a0001c0002t0001g0032 a0001c0002t0001g0060 a0002c0005t0001g0025 |
3 | HG02486.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1327-42_1327-41ins others(512): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(537): Show |
1 | a0001c0002t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1327-42_1327-41ins others(544): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | A | AAGAAGGA others(569): Show |
1 | a0001c0002t0001g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1327-42_1327-41ins others(576): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | AAGAAGGA others(25): Show |
A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0132 a0001c0001t0001g0136 others(3): Show |
6 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1327-73_1327-42del others(32): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | AAGAAGGA others(57): Show |
A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0172 |
2 | HG00280.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1327-105_1327-42de others(65): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721071 | AAGAAGGA others(89): Show |
A | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1327-137_1327-42de others(97): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chrX | 111721071 | ||||||
| chrX:111721716 | A | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
splice_region_variant&intron_variant | LOW | c.1435+5A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 12/26 | chrX | 111721716 | |||||||
| chrX:111722341 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1436-452G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 12/26 | chrX | 111722341 | |||||||
| chrX:111723112 | T | G | 1 | a0002c0005t0001g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1500+255T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | chrX | 111723112 | |||||||
| chrX:111723153 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1500+296A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | chrX | 111723153 | |||||||
| chrX:111723415 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1501-383G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | chrX | 111723415 | |||||||
| chrX:111723500 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02451.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1501-298G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 13/26 | chrX | 111723500 | |||||||
| chrX:111724032 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1601+134T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 14/26 | chrX | 111724032 | |||||||
| chrX:111724740 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1602-194C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 14/26 | chrX | 111724740 | |||||||
| chrX:111725122 | G | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
70 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.1729+61G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111725122 | |||||||
| chrX:111725199 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1729+138T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111725199 | |||||||
| chrX:111725603 | G | T | 1 | a0001c0002t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1729+542G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111725603 | |||||||
| chrX:111726007 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1730-802T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726007 | |||||||
| chrX:111726045 | G | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730-764G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726045 | |||||||
| chrX:111726132 | A | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1730-677A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726132 | |||||||
| chrX:111726232 | G | GT | 29 | a0001c0001t0001g0007 a0001c0001t0001g0069 a0001c0001t0001g0071 others(26): Show |
29 | HG00642.hp1 HG01192.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1730-556dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chrX | 111726232 | ||||||
| chrX:111726232 | G | GTT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0068 others(6): Show |
9 | HG02056.hp1 HG02257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1730-557_1730-556d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chrX | 111726232 | ||||||
| chrX:111726232 | GT | G | 39 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(36): Show |
40 | HG00558.hp2 HG01106.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1730-556delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chrX | 111726232 | ||||||
| chrX:111726415 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1730-394G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726415 | |||||||
| chrX:111726422 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18990.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1730-387C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726422 | |||||||
| chrX:111726424 | G | A | 22 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0020 others(19): Show |
23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1730-385G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 15/26 | chrX | 111726424 | |||||||
| chrX:111728143 | A | G | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2248-42A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 18/26 | chrX | 111728143 | |||||||
| chrX:111728181 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp1 | splice_region_variant&intron_variant | LOW | c.2248-4A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 18/26 | chrX | 111728181 | |||||||
| chrX:111728706 | C | T | 25 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0019 others(22): Show |
26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2368+401C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111728706 | |||||||
| chrX:111728796 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2368+491T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111728796 | |||||||
| chrX:111728924 | T | C | 1 | a0001c0002t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2368+619T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111728924 | |||||||
| chrX:111729247 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2368+942T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729247 | |||||||
| chrX:111729296 | T | C | 20 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2368+991T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729296 | |||||||
| chrX:111729444 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2369-951G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729444 | |||||||
| chrX:111729597 | A | G | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2369-798A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729597 | |||||||
| chrX:111729714 | C | T | 1 | a0001c0002t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369-681C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729714 | |||||||
| chrX:111729726 | G | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
70 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.2369-669G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729726 | |||||||
| chrX:111729818 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2369-577A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729818 | |||||||
| chrX:111729923 | T | C | 4 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0059 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2369-472T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111729923 | |||||||
| chrX:111730297 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2369-98A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 19/26 | chrX | 111730297 | |||||||
| chrX:111730439 | C | A | 1 | a0001c0002t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2401+12C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 20/26 | chrX | 111730439 | |||||||
| chrX:111730613 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2457+33T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111730613 | |||||||
| chrX:111731018 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2457+438C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111731018 | |||||||
| chrX:111731452 | A | G | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2457+872A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111731452 | |||||||
| chrX:111731588 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2457+1008C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111731588 | |||||||
| chrX:111731739 | G | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
70 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.2457+1159G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111731739 | |||||||
| chrX:111732013 | G | A | 7 | a0001c0001t0001g0113 a0001c0001t0001g0120 a0001c0001t0001g0122 others(4): Show |
7 | HG01934.hp1 NA18944.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.2457+1433G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732013 | |||||||
| chrX:111732150 | A | G | 2 | a0001c0001t0001g0100 a0005c0012t0001g0101 |
2 | HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2457+1570A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732150 | |||||||
| chrX:111732370 | T | C | 1 | a0002c0003t0001g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2457+1790T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732370 | |||||||
| chrX:111732770 | C | T | 1 | a0001c0002t0001g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2457+2190C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732770 | |||||||
| chrX:111732849 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2458-2202A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111732849 | |||||||
| chrX:111733058 | C | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(7): Show |
10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2458-1993C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733058 | |||||||
| chrX:111733067 | A | G | 1 | a0006c0011t0001g0165 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2458-1984A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733067 | |||||||
| chrX:111733262 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2458-1789A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733262 | |||||||
| chrX:111733287 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2458-1764C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733287 | |||||||
| chrX:111733379 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2458-1672A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733379 | |||||||
| chrX:111733409 | A | G | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2458-1642A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733409 | |||||||
| chrX:111733426 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2458-1625G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733426 | |||||||
| chrX:111733464 | T | G | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2458-1587T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111733464 | |||||||
| chrX:111734160 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2458-891C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111734160 | |||||||
| chrX:111734589 | G | A | 1 | a0007c0015t0001g0129 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2458-462G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111734589 | |||||||
| chrX:111734667 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2458-384G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 21/26 | chrX | 111734667 | |||||||
| chrX:111735131 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2529+9C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111735131 | |||||||
| chrX:111735397 | C | T | 2 | a0001c0001t0001g0100 a0005c0012t0001g0101 |
2 | HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2529+275C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111735397 | |||||||
| chrX:111735712 | G | A | 1 | a0001c0002t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2529+590G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111735712 | |||||||
| chrX:111736404 | G | T | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2530-310G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111736404 | |||||||
| chrX:111736452 | C | T | 26 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0019 others(23): Show |
27 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.2530-262C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 22/26 | chrX | 111736452 | |||||||
| chrX:111736926 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2695+47A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111736926 | |||||||
| chrX:111737317 | C | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+438C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111737317 | |||||||
| chrX:111737334 | T | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0152 a0002c0003t0001g0111 others(2): Show |
5 | HG01192.hp1 NA18953.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.2695+455T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111737334 | |||||||
| chrX:111738135 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2695+1256A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738135 | |||||||
| chrX:111738222 | G | A | 1 | a0001c0002t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2695+1343G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738222 | |||||||
| chrX:111738247 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01884.hp1 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2695+1368T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738247 | |||||||
| chrX:111738415 | G | A | 1 | a0002c0003t0001g0179 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2695+1536G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738415 | |||||||
| chrX:111738479 | G | C | 4 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0032 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+1600G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738479 | |||||||
| chrX:111738499 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2695+1620C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738499 | |||||||
| chrX:111738797 | A | G | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+1918A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738797 | |||||||
| chrX:111738945 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(6): Show |
9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2695+2066A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111738945 | |||||||
| chrX:111739369 | A | C | 1 | a0001c0002t0001g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2695+2490A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739369 | |||||||
| chrX:111739397 | A | G | 4 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0059 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2695+2518A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739397 | |||||||
| chrX:111739584 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2695+2705T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739584 | |||||||
| chrX:111739855 | T | C | 1 | a0001c0002t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2695+2976T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739855 | |||||||
| chrX:111739877 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2695+2998C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111739877 | |||||||
| chrX:111740735 | A | G | 1 | a0001c0002t0001g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2695+3856A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111740735 | |||||||
| chrX:111741196 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2696-3472T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741196 | |||||||
| chrX:111741204 | G | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(8): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2696-3464G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741204 | |||||||
| chrX:111741394 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(8): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2696-3274A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741394 | |||||||
| chrX:111741406 | A | G | 1 | a0002c0003t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2696-3262A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741406 | |||||||
| chrX:111741782 | C | T | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2696-2886C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741782 | |||||||
| chrX:111741810 | C | CA | 6 | a0001c0001t0001g0048 a0001c0001t0001g0085 a0001c0001t0001g0143 others(3): Show |
6 | HG01106.hp1 HG02132.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2696-2842dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111741810 | ||||||
| chrX:111741810 | CA | C | 27 | a0001c0001t0001g0082 a0001c0001t0001g0166 a0001c0001t0001g0168 others(24): Show |
28 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2696-2842delA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111741810 | ||||||
| chrX:111741825 | A | T | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2696-2843A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111741825 | |||||||
| chrX:111742090 | A | G | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-2578A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742090 | |||||||
| chrX:111742653 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2696-2015G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742653 | |||||||
| chrX:111742729 | G | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
6 | NA18943.hp1 NA18959.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.2696-1939G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742729 | |||||||
| chrX:111742833 | G | A | 22 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0020 others(19): Show |
23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2696-1835G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742833 | |||||||
| chrX:111742981 | A | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2696-1687A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111742981 | |||||||
| chrX:111743069 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2696-1599C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111743069 | |||||||
| chrX:111743752 | C | G | 25 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0019 others(22): Show |
26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2696-916C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111743752 | |||||||
| chrX:111743906 | T | TAA | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(7): Show |
10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2696-751_2696-750d others(4): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chrX | 111743906 | ||||||
| chrX:111743916 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2696-752A>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111743916 | |||||||
| chrX:111744164 | G | A | 20 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2696-504G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 23/26 | chrX | 111744164 | |||||||
| chrX:111744994 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2932+90G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111744994 | |||||||
| chrX:111745767 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2932+863A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111745767 | |||||||
| chrX:111746184 | T | C | 1 | a0001c0006t0001g0154 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2932+1280T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111746184 | |||||||
| chrX:111746405 | T | G | 22 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0020 others(19): Show |
23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2932+1501T>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111746405 | |||||||
| chrX:111746966 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2932+2062T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111746966 | |||||||
| chrX:111746977 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(6): Show |
9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2932+2073C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111746977 | |||||||
| chrX:111747190 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2932+2286G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111747190 | |||||||
| chrX:111747579 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2932+2675C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111747579 | |||||||
| chrX:111747592 | T | C | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2932+2688T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111747592 | |||||||
| chrX:111747636 | A | G | 1 | a0001c0002t0001g0002 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2932+2732A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111747636 | |||||||
| chrX:111748478 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2932+3574G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111748478 | |||||||
| chrX:111748817 | T | A | 1 | a0001c0002t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2932+3913T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111748817 | |||||||
| chrX:111748841 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2932+3937C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111748841 | |||||||
| chrX:111748864 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG02615.hp1 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2933-3926A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111748864 | |||||||
| chrX:111749116 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2933-3674C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749116 | |||||||
| chrX:111749145 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2933-3645C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749145 | |||||||
| chrX:111749485 | C | G | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2933-3305C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749485 | |||||||
| chrX:111749501 | C | CA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0077 others(16): Show |
19 | HG00558.hp1 HG01243.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.2933-3276dupA | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111749501 | ||||||
| chrX:111749515 | C | G | 1 | a0001c0002t0001g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2933-3275C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749515 | |||||||
| chrX:111749572 | A | G | 19 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
19 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2933-3218A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111749572 | |||||||
| chrX:111749959 | CTT | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0115 a0001c0001t0001g0133 |
3 | NA18974.hp1 NA19005.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2933-2829_2933-282 others(6): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111749959 | ||||||
| chrX:111750084 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2933-2706T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111750084 | |||||||
| chrX:111750551 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2933-2239A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111750551 | |||||||
| chrX:111750619 | AGTATT | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0173 |
2 | HG02074.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.2933-2158_2933-215 others(9): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111750619 | ||||||
| chrX:111750632 | ATTGT | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2933-2143_2933-214 others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111750632 | ||||||
| chrX:111750656 | C | CTTAT | 5 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0170 others(2): Show |
5 | HG00140.hp1 HG00738.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933-2107_2933-210 others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111750656 | ||||||
| chrX:111750656 | CTTAT | C | 3 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0183 |
3 | HG02109.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2933-2107_2933-210 others(8): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111750656 | ||||||
| chrX:111750692 | T | C | 1 | a0001c0002t0001g0030 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2933-2098T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111750692 | |||||||
| chrX:111751066 | C | CT | 5 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0128 others(2): Show |
5 | HG00609.hp1 HG03516.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933-1703dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111751066 | ||||||
| chrX:111751066 | CT | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0036 others(52): Show |
57 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.2933-1703delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chrX | 111751066 | ||||||
| chrX:111751092 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2933-1698C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751092 | |||||||
| chrX:111751342 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2933-1448C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751342 | |||||||
| chrX:111751358 | C | T | 22 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0020 others(19): Show |
23 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2933-1432C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751358 | |||||||
| chrX:111751564 | G | A | 1 | a0001c0002t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2933-1226G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751564 | |||||||
| chrX:111751625 | C | G | 5 | a0001c0001t0001g0082 a0001c0001t0001g0166 a0001c0001t0001g0168 others(2): Show |
5 | NA18952.hp1 NA18970.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933-1165C>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751625 | |||||||
| chrX:111751724 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2933-1066T>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751724 | |||||||
| chrX:111751849 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2933-941G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111751849 | |||||||
| chrX:111752426 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2933-364T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752426 | |||||||
| chrX:111752447 | G | A | 2 | a0001c0001t0001g0044 a0004c0009t0001g0043 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2933-343G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752447 | |||||||
| chrX:111752485 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2933-305G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752485 | |||||||
| chrX:111752576 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2933-214C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752576 | |||||||
| chrX:111752733 | A | G | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2933-57A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 24/26 | chrX | 111752733 | |||||||
| chrX:111753539 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2973+709G>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111753539 | |||||||
| chrX:111753766 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2973+936A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111753766 | |||||||
| chrX:111754008 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2973+1178G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754008 | |||||||
| chrX:111754023 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2973+1193A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754023 | |||||||
| chrX:111754358 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2973+1528C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754358 | |||||||
| chrX:111754360 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2973+1530G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754360 | |||||||
| chrX:111754433 | G | A | 25 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0019 others(22): Show |
26 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2973+1603G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754433 | |||||||
| chrX:111754965 | C | T | 37 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(34): Show |
37 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.2973+2135C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111754965 | |||||||
| chrX:111755549 | T | C | 1 | a0001c0002t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2974-2039T>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111755549 | |||||||
| chrX:111755572 | A | AAATTTAC others(3): Show |
2 | a0001c0001t0001g0108 a0002c0003t0001g0151 |
2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2974-2013_2974-200 others(14): Show |
ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | 111755572 | ||||||
| chrX:111755678 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2974-1910A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111755678 | |||||||
| chrX:111756152 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(7): Show |
10 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2974-1436A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756152 | |||||||
| chrX:111756160 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2974-1428G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756160 | |||||||
| chrX:111756255 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2974-1333C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756255 | |||||||
| chrX:111756261 | C | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(60): Show |
64 | HG01106.hp1 HG01109.hp1 HG01884.hp1 others(61): Show |
intron_variant | MODIFIER | c.2974-1327C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756261 | |||||||
| chrX:111756262 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2974-1326G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756262 | |||||||
| chrX:111756263 | G | C | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2974-1325G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756263 | |||||||
| chrX:111756383 | A | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(6): Show |
9 | HG02257.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2974-1205A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756383 | |||||||
| chrX:111756489 | C | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2974-1099C>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111756489 | |||||||
| chrX:111757248 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2974-340G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111757248 | |||||||
| chrX:111757400 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2974-188A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111757400 | |||||||
| chrX:111757493 | A | AT | 7 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0113 others(4): Show |
7 | HG01255.hp1 HG01515.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2974-79dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chrX | 111757493 | ||||||
| chrX:111757547 | A | C | 4 | a0003c0004t0001g0009 a0003c0004t0001g0065 a0003c0004t0001g0066 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2974-41A>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 25/26 | chrX | 111757547 | |||||||
| chrX:111758317 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
74 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.3148+555G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111758317 | |||||||
| chrX:111758444 | A | G | 1 | a0002c0008t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3148+682A>G | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111758444 | |||||||
| chrX:111758475 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3148+713C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111758475 | |||||||
| chrX:111758827 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3149-907C>T | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111758827 | |||||||
| chrX:111759144 | A | AT | 10 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0085 others(7): Show |
10 | HG01928.hp1 HG01943.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.3149-572dupT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | 111759144 | ||||||
| chrX:111759144 | AT | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
35 | HG01256.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.3149-572delT | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chrX | 111759144 | ||||||
| chrX:111759343 | G | C | 1 | a0006c0011t0001g0165 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3149-391G>C | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111759343 | |||||||
| chrX:111759595 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
6 | NA18943.hp1 NA18959.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.3149-139G>A | ALG13 | ENSG00000101901.13 | transcript | ENST00000394780.8 | protein_coding | 26/26 | chrX | 111759595 |