Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 139322 |
| ensemblid | ENSG00000155008.16 |
| hgncid | 24009 |
| symbol | APOOL |
| name | apolipoprotein O like |
| refseq_nuc | NM_198450.6 |
| refseq_prot | NP_940852.3 |
| ensembl_nuc | ENST00000373173.7 |
| ensembl_prot | ENSP00000362268.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 85003877 |
| end | 85093315 |
| strand | + |
| ver | v1.2 |
| region | chrX:85003877-85093315 |
| region5000 | chrX:84998877-85098315 |
| regionname0 | APOOL_chrX_85003877_85093315 |
| regionname5000 | APOOL_chrX_84998877_85098315 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 268 | 255 | 72 | 48 | 106 | 7 | 20 | 86 | APOOL_chrX_84998877_85098315 | APOOL | MAAIR others(263): Show |
chrX | 84998877 | 85098315 |
| a0002 | 0/0 | 268 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | MAAIR others(263): Show |
chrX | 84998877 | 85098315 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 804 | 255 | 72 | 48 | 106 | 7 | 20 | APOOL_chrX_84998877_85098315 | APOOL | ATGGC others(799): Show |
chrX | 84998877 | 85098315 | ||
| a0002c0002 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | ATGGC others(799): Show |
chrX | 84998877 | 85098315 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6343 | 37 | 0 | 6 | 24 | 1 | 6 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6338): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0002 | 0/0 | 6344 | 26 | 0 | 9 | 13 | 1 | 3 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6339): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0003 | 0/0 | 6342 | 15 | 2 | 1 | 11 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6337): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0004 | 0/0 | 6429 | 10 | 8 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6424): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0005 | 0/0 | 6345 | 9 | 0 | 4 | 3 | 1 | 1 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6340): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0006 | 0/0 | 6482 | 7 | 1 | 0 | 4 | 2 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6477): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0007 | 0/0 | 6429 | 5 | 3 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6424): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0008 | 0/0 | 6344 | 5 | 0 | 0 | 5 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6339): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0009 | 0/0 | 6346 | 5 | 5 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6341): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0010 | 0/0 | 6483 | 4 | 4 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6478): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0011 | 0/0 | 6478 | 4 | 0 | 0 | 4 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6473): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0012 | 0/0 | 6338 | 4 | 4 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6333): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0013 | 0/0 | 6341 | 4 | 4 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6336): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0014 | 0/0 | 6429 | 3 | 0 | 0 | 3 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6424): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0015 | 0/0 | 6430 | 3 | 2 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6425): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0016 | 0/0 | 6482 | 3 | 3 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6477): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0017 | 0/0 | 6331 | 3 | 3 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6326): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0018 | 0/0 | 6338 | 3 | 2 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6333): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0019 | 0/0 | 6342 | 3 | 0 | 1 | 0 | 0 | 2 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6337): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0020 | 0/0 | 6346 | 3 | 0 | 1 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6341): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0021 | 0/0 | 6414 | 3 | 3 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6409): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0022 | 0/0 | 6426 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6421): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0023 | 0/0 | 6429 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6424): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0024 | 0/0 | 6483 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6478): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0025 | 0/0 | 6477 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6472): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0026 | 0/0 | 6343 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6338): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0027 | 0/0 | 6343 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6338): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0028 | 0/0 | 6344 | 2 | 0 | 0 | 0 | 0 | 2 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6339): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0029 | 0/0 | 6343 | 2 | 0 | 1 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6338): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0030 | 0/0 | 6346 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6341): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0031 | 0/0 | 6331 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6326): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0032 | 0/0 | 7152 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7147): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0033 | 0/0 | 6970 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6965): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0034 | 0/0 | 7004 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6999): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0035 | 0/0 | 6938 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6933): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0036 | 0/0 | 7058 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7053): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0037 | 0/1 | 6970 | 2 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6965): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0038 | 0/0 | 6434 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6429): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0039 | 0/0 | 6434 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6429): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0040 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6532): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0041 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6563): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0042 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6423): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0043 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6424): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0044 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6425): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0045 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6972): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0046 | 0/0 | 7005 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7000): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0047 | 0/0 | 6625 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6620): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0048 | 0/0 | 6485 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6480): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0049 | 1/0 | 6480 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6475): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0050 | 0/0 | 6432 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6427): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0051 | 0/0 | 6484 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6479): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0052 | 0/0 | 6436 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6431): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0053 | 0/0 | 6512 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6507): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0054 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6473): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0055 | 0/0 | 6340 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6335): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0056 | 0/0 | 6343 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6338): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0057 | 0/0 | 6342 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6337): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0058 | 0/0 | 6344 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6339): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0059 | 0/0 | 6344 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6339): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0060 | 0/0 | 6345 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6340): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0061 | 0/0 | 6345 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6340): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0062 | 0/0 | 7006 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7001): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0063 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6752): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0064 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6752): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0065 | 0/0 | 7125 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7120): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0066 | 0/0 | 7122 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7117): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0067 | 0/0 | 7123 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7118): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0068 | 0/0 | 6938 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6933): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0069 | 0/0 | 7002 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6997): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0070 | 0/0 | 7000 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6995): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0071 | 0/0 | 7003 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6998): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0072 | 0/0 | 7004 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6999): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0073 | 0/0 | 7003 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6998): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0074 | 0/0 | 6970 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6965): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0075 | 0/0 | 6992 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6987): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0076 | 0/0 | 6970 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6965): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0077 | 0/0 | 6971 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6966): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0078 | 0/0 | 7002 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6997): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0079 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7028): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0080 | 0/0 | 6939 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6934): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0081 | 0/0 | 6968 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6963): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0082 | 0/0 | 6938 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6933): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0083 | 0/0 | 7002 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6997): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0084 | 0/0 | 7120 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7115): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0085 | 0/0 | 7088 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7083): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0086 | 0/0 | 7101 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7096): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0087 | 0/0 | 7002 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6997): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0088 | 0/0 | 7002 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6997): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0089 | 0/0 | 7001 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6996): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0090 | 0/0 | 7002 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6997): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0091 | 0/0 | 6938 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6933): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0092 | 0/0 | 6939 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6934): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0093 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6904): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0094 | 0/0 | 6968 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6963): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0095 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7118): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0096 | 0/0 | 6996 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6991): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0097 | 0/0 | 6480 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6475): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0098 | 0/0 | 6481 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6476): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0099 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6503): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0100 | 0/0 | 6480 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6475): Show |
chrX | 84998877 | 85098315 |
| a0001c0001t0101 | 0/0 | 7097 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(7092): Show |
chrX | 84998877 | 85098315 |
| a0002c0002t0007 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | CTCCG others(6424): Show |
chrX | 84998877 | 85098315 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0007g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0007g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0012g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0013g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0014g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0014g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0014g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0015g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0015g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0016g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0016g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0017g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0017g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0017g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0018g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0018g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0018g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0019g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0019g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0019g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0020g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0020g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0020g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0021g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0021g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0021g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0022g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0023g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0023g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0024g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0024g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0025g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0025g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0026g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0026g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0027g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0028g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0028g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0029g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0029g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0030g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0030g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0031g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0031g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0032g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0033g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0033g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0034g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0034g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0035g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0035g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0036g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0036g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0037g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0037g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0038g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0039g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0040g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0041g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0042g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0043g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0044g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0045g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0046g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0047g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0048g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0049g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0050g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0051g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0052g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0053g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0054g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0055g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0056g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0057g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0058g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0059g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0060g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0061g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0062g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0063g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0064g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0065g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0066g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0067g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0068g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0069g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0070g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0071g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0072g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0073g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0074g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0075g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0076g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0077g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0078g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0079g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0080g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0081g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0082g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0083g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0084g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0085g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0086g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0087g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0088g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0089g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0090g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0091g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0092g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0093g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0094g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0095g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0096g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0097g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0098g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0099g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0100g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0001c0001t0101g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| a0002c0002t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0093 | EUR | FIN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00438 | hp1 | a0001 | c0001 | t0095 | g0075 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0070 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00621 | hp1 | a0001 | c0001 | t0079 | g0045 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00673 | hp1 | a0001 | c0001 | t0011 | g0042 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00733 | hp1 | a0001 | c0001 | t0062 | g0072 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00735 | hp1 | a0001 | c0001 | t0093 | g0020 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG00738 | hp1 | a0001 | c0001 | t0015 | g0237 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01069 | hp1 | a0001 | c0001 | t0036 | g0063 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01071 | hp1 | a0001 | c0001 | t0036 | g0003 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01074 | hp1 | a0001 | c0001 | t0033 | g0046 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01081 | hp1 | a0001 | c0001 | t0069 | g0056 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01106 | hp1 | a0001 | c0001 | t0073 | g0030 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0224 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0243 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01168 | hp2 | a0001 | c0001 | t0070 | g0055 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0236 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01175 | hp2 | a0001 | c0001 | t0033 | g0049 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01243 | hp1 | a0001 | c0001 | t0018 | g0167 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01255 | hp1 | a0001 | c0001 | t0019 | g0199 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01256 | hp1 | a0001 | c0001 | t0029 | g0107 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01257 | hp1 | a0001 | c0001 | t0032 | g0005 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01258 | hp1 | a0001 | c0001 | t0032 | g0005 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01346 | hp2 | a0001 | c0001 | t0076 | g0014 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01358 | hp1 | a0001 | c0001 | t0072 | g0079 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01361 | hp1 | a0001 | c0001 | t0083 | g0059 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0092 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0210 | EUR | IBS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01517 | hp1 | a0001 | c0001 | t0029 | g0136 | EUR | IBS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0211 | EUR | IBS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0197 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01884 | hp2 | a0001 | c0001 | t0044 | g0212 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01891 | hp1 | a0001 | c0001 | t0058 | g0208 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01891 | hp2 | a0001 | c0001 | t0054 | g0050 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01928 | hp1 | a0001 | c0001 | t0067 | g0081 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0206 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0148 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01978 | hp2 | a0001 | c0001 | t0020 | g0122 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02004 | hp1 | a0001 | c0001 | t0091 | g0149 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02004 | hp2 | a0001 | c0001 | t0066 | g0082 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02015 | hp1 | a0001 | c0001 | t0096 | g0043 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02040 | hp1 | a0001 | c0001 | t0008 | g0207 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02055 | hp1 | a0001 | c0001 | t0051 | g0221 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02056 | hp1 | a0001 | c0001 | t0020 | g0174 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02071 | hp1 | a0001 | c0001 | t0094 | g0026 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02074 | hp1 | a0001 | c0001 | t0075 | g0038 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02135 | hp1 | a0001 | c0001 | t0082 | g0060 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0220 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0071 | EAS | CDX | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | CDX | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02257 | hp1 | a0001 | c0001 | t0031 | g0113 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0163 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02273 | hp2 | a0001 | c0001 | t0065 | g0083 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02280 | hp2 | a0001 | c0001 | t0063 | g0015 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02451 | hp1 | a0002 | c0002 | t0007 | g0239 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02451 | hp2 | a0001 | c0001 | t0027 | g0008 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02602 | hp1 | a0001 | c0001 | t0019 | g0151 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0120 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02615 | hp2 | a0001 | c0001 | t0026 | g0190 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02622 | hp1 | a0001 | c0001 | t0021 | g0074 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02630 | hp1 | a0001 | c0001 | t0018 | g0192 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02630 | hp2 | a0001 | c0001 | t0040 | g0234 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0240 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02723 | hp1 | a0001 | c0001 | t0016 | g0219 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02723 | hp2 | a0001 | c0001 | t0025 | g0021 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0112 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02738 | hp1 | a0001 | c0001 | t0057 | g0141 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02809 | hp1 | a0001 | c0001 | t0015 | g0235 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02818 | hp1 | a0001 | c0001 | t0047 | g0010 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02818 | hp2 | a0001 | c0001 | t0021 | g0073 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0194 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02895 | hp1 | a0001 | c0001 | t0023 | g0244 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0196 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02897 | hp1 | a0001 | c0001 | t0023 | g0238 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02897 | hp2 | a0001 | c0001 | t0060 | g0195 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0185 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02922 | hp2 | a0001 | c0001 | t0042 | g0228 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02965 | hp1 | a0001 | c0001 | t0026 | g0161 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02970 | hp1 | a0001 | c0001 | t0022 | g0009 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02970 | hp2 | a0001 | c0001 | t0016 | g0053 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0162 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03017 | hp1 | a0001 | c0001 | t0028 | g0198 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03041 | hp1 | a0001 | c0001 | t0048 | g0218 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03041 | hp2 | a0001 | c0001 | t0016 | g0054 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0087 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0117 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03195 | hp1 | a0001 | c0001 | t0055 | g0007 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03195 | hp2 | a0001 | c0001 | t0031 | g0156 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0245 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0100 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0121 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03486 | hp1 | a0001 | c0001 | t0041 | g0217 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0193 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03516 | hp1 | a0001 | c0001 | t0022 | g0009 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0007 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03579 | hp1 | a0001 | c0001 | t0017 | g0119 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03688 | hp1 | a0001 | c0001 | t0059 | g0143 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03704 | hp1 | a0001 | c0001 | t0053 | g0065 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03704 | hp2 | a0001 | c0001 | t0028 | g0178 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03710 | hp1 | a0001 | c0001 | t0086 | g0031 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03831 | hp1 | a0001 | c0001 | t0046 | g0039 | SAS | BEB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | BEB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG04228 | hp1 | a0001 | c0001 | t0019 | g0181 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18522 | hp1 | a0001 | c0001 | t0027 | g0008 | AFR | YRI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | CHB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CHB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18906 | hp1 | a0001 | c0001 | t0015 | g0242 | AFR | YRI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | YRI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0186 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18950 | hp2 | a0001 | c0001 | t0090 | g0061 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18952 | hp1 | a0001 | c0001 | t0014 | g0215 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18953 | hp1 | a0001 | c0001 | t0014 | g0214 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0150 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18954 | hp2 | a0001 | c0001 | t0034 | g0078 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18959 | hp1 | a0001 | c0001 | t0074 | g0233 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18962 | hp1 | a0001 | c0001 | t0008 | g0155 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18963 | hp2 | a0001 | c0001 | t0078 | g0033 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18964 | hp2 | a0001 | c0001 | t0011 | g0018 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18965 | hp1 | a0001 | c0001 | t0030 | g0152 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18967 | hp1 | a0001 | c0001 | t0024 | g0019 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18968 | hp1 | a0001 | c0001 | t0043 | g0213 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18969 | hp1 | a0001 | c0001 | t0084 | g0076 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18969 | hp2 | a0001 | c0001 | t0056 | g0145 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18971 | hp1 | a0001 | c0001 | t0081 | g0004 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18975 | hp2 | a0001 | c0001 | t0077 | g0036 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18977 | hp1 | a0001 | c0001 | t0098 | g0032 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18981 | hp1 | a0001 | c0001 | t0050 | g0052 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18982 | hp1 | a0001 | c0001 | t0088 | g0069 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18992 | hp1 | a0001 | c0001 | t0089 | g0037 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18995 | hp1 | a0001 | c0001 | t0068 | g0002 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18998 | hp2 | a0001 | c0001 | t0097 | g0066 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19000 | hp1 | a0001 | c0001 | t0024 | g0027 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19001 | hp1 | a0001 | c0001 | t0020 | g0188 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19001 | hp2 | a0001 | c0001 | t0035 | g0004 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19006 | hp1 | a0001 | c0001 | t0080 | g0025 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19011 | hp1 | a0001 | c0001 | t0011 | g0067 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19011 | hp2 | a0001 | c0001 | t0014 | g0216 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0017 | AFR | LWK | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0094 | AFR | LWK | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19043 | hp1 | a0001 | c0001 | t0052 | g0164 | AFR | LWK | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19057 | hp2 | a0001 | c0001 | t0071 | g0062 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19065 | hp2 | a0001 | c0001 | t0101 | g0068 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19066 | hp1 | a0001 | c0001 | t0035 | g0034 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19068 | hp1 | a0001 | c0001 | t0045 | g0044 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19070 | hp1 | a0001 | c0001 | t0037 | g0041 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19074 | hp1 | a0001 | c0001 | t0008 | g0154 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19086 | hp1 | a0001 | c0001 | t0085 | g0077 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19087 | hp1 | a0001 | c0001 | t0061 | g0187 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19087 | hp2 | a0001 | c0001 | t0100 | g0029 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19088 | hp1 | a0001 | c0001 | t0030 | g0153 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA19091 | hp1 | a0001 | c0001 | t0034 | g0080 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | ASW | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0200 | AFR | ASW | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA20752 | hp1 | a0001 | c0001 | t0092 | g0035 | EUR | TSI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0006 | EUR | TSI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0202 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG01123 | hp2 | a0001 | c0001 | t0087 | g0003 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02109 | hp1 | a0001 | c0001 | t0039 | g0023 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02109 | hp2 | a0001 | c0001 | t0064 | g0047 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02486 | hp1 | a0001 | c0001 | t0017 | g0191 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02559 | hp1 | a0001 | c0001 | t0038 | g0022 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0013 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG03471 | hp1 | a0001 | c0001 | t0021 | g0048 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0241 | AFR | USA | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | USA | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| NA18955 | hp1 | a0001 | c0001 | t0099 | g0040 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0037 | g0051 | REF | REF | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0049 | g0064 | REF | REF | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
| 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:85074095 | C | G | 1 | a0002 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.584C>G | p.Pro195Arg | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 7/9 | 620/6480 | 584/807 | 195/268 | chrX | 85074095 |
| 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 |
|---|
| 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:85087777 | G | A | 2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*99G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 99 | chrX | 85087777 | ||||||
| chrX:85087993 | CAT | C | 5 | a0001c0001t0097 a0001c0001t0098 a0001c0001t0099 others(2): Show |
5 | NA18955.hp1 NA18977.hp1 NA18998.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*326_*327delAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 326 | INFO_REALIGN_3_PRIME | chrX | 85087993 | |||||
| chrX:85088003 | T | C | 1 | a0001c0001t0022 | 2 | HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*325T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 325 | chrX | 85088003 | ||||||
| chrX:85088015 | AATAC | A | 2 | a0001c0001t0021 a0001c0001t0022 |
5 | HG02622.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*345_*348delCATA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 345 | INFO_REALIGN_3_PRIME | chrX | 85088015 | |||||
| chrX:85088016 | A | G | 2 | a0001c0001t0036 a0001c0001t0087 |
3 | HG01069.hp1 HG01071.hp1 HG01123.hp2 |
3_prime_UTR_variant | MODIFIER | c.*338A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 338 | chrX | 85088016 | ||||||
| chrX:85088046 | G | GTATTAAT others(457): Show |
1 | a0001c0001t0045 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372_*373insAATACA others(458): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 373 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTAAT others(485): Show |
1 | a0001c0001t0046 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372_*373insAATACA others(486): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 373 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(455): Show |
1 | a0001c0001t0062 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(456): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(267): Show |
1 | a0001c0001t0063 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(268): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(267): Show |
1 | a0001c0001t0064 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(268): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(605): Show |
1 | a0001c0001t0065 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(606): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(603): Show |
1 | a0001c0001t0066 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(604): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(633): Show |
1 | a0001c0001t0032 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(634): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(603): Show |
1 | a0001c0001t0067 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(604): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(453): Show |
1 | a0001c0001t0068 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(454): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(451): Show |
3 | a0001c0001t0033 a0001c0001t0069 a0001c0001t0070 |
4 | HG01074.hp1 HG01081.hp1 HG01168.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(481): Show |
1 | a0001c0001t0071 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(482): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(485): Show |
2 | a0001c0001t0034 a0001c0001t0072 |
3 | HG01358.hp1 NA18954.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(486): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(483): Show |
1 | a0001c0001t0073 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(484): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(421): Show |
1 | a0001c0001t0074 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(422): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(451): Show |
2 | a0001c0001t0076 a0001c0001t0077 |
2 | HG01346.hp2 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(481): Show |
2 | a0001c0001t0078 a0001c0001t0079 |
2 | HG00621.hp1 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(482): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(419): Show |
2 | a0001c0001t0035 a0001c0001t0080 |
3 | NA19001.hp2 NA19006.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(449): Show |
1 | a0001c0001t0081 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(450): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(419): Show |
1 | a0001c0001t0082 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(483): Show |
1 | a0001c0001t0083 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(484): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(601): Show |
1 | a0001c0001t0084 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(602): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(569): Show |
1 | a0001c0001t0085 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(570): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(581): Show |
1 | a0001c0001t0086 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(582): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(517): Show |
1 | a0001c0001t0101 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(518): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(451): Show |
1 | a0001c0001t0087 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(483): Show |
1 | a0001c0001t0088 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(484): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(451): Show |
1 | a0001c0001t0037 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(481): Show |
2 | a0001c0001t0089 a0001c0001t0090 |
2 | NA18950.hp2 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(482): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(419): Show |
2 | a0001c0001t0091 a0001c0001t0092 |
2 | HG02004.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(357): Show |
1 | a0001c0001t0093 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(358): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(417): Show |
1 | a0001c0001t0094 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(418): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(539): Show |
1 | a0001c0001t0095 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(540): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088046 | G | GTATTTAT others(477): Show |
1 | a0001c0001t0096 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(478): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | |||||
| chrX:85088050 | T | G | 3 | a0001c0001t0021 a0001c0001t0040 a0001c0001t0041 |
5 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*372T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 372 | chrX | 85088050 | ||||||
| chrX:85088050 | T | TTATACAT others(473): Show |
1 | a0001c0001t0075 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(474): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088050 | |||||
| chrX:85088050 | T | TTATACAT others(505): Show |
1 | a0001c0001t0036 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(506): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088050 | |||||
| chrX:85088051 | T | A | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(6): Show |
27 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*373T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 373 | chrX | 85088051 | ||||||
| chrX:85088055 | C | CATATATA others(183): Show |
1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383_*384insATGTAT others(184): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 384 | INFO_REALIGN_3_PRIME | chrX | 85088055 | |||||
| chrX:85088067 | AATACATA others(81): Show |
A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*398_*485delACATAT others(82): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 398 | INFO_REALIGN_3_PRIME | chrX | 85088067 | |||||
| chrX:85088071 | C | CGTATGTA others(279): Show |
1 | a0001c0001t0021 | 2 | HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATGT others(280): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATGTA others(247): Show |
1 | a0001c0001t0021 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATGT others(248): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(341): Show |
2 | a0001c0001t0025 a0001c0001t0054 |
2 | HG01891.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(342): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(341): Show |
1 | a0001c0001t0025 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(342): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(431): Show |
1 | a0001c0001t0011 | 2 | HG00673.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(432): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(431): Show |
1 | a0001c0001t0011 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(432): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(431): Show |
1 | a0001c0001t0011 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(432): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(611): Show |
1 | a0001c0001t0006 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(612): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(419): Show |
1 | a0001c0001t0006 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(449): Show |
1 | a0001c0001t0053 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(450): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(451): Show |
1 | a0001c0001t0006 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(607): Show |
1 | a0001c0001t0099 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(608): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(637): Show |
1 | a0001c0001t0098 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(638): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(615): Show |
1 | a0001c0001t0100 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(616): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(397): Show |
1 | a0001c0001t0024 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(398): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(429): Show |
1 | a0001c0001t0006 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(430): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(461): Show |
1 | a0001c0001t0006 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(462): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(265): Show |
1 | a0001c0001t0051 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(266): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(113): Show |
1 | a0001c0001t0016 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(114): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(637): Show |
1 | a0001c0001t0097 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(638): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(351): Show |
1 | a0001c0001t0048 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(352): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(361): Show |
1 | a0001c0001t0010 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(362): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(359): Show |
1 | a0001c0001t0010 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(360): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(297): Show |
1 | a0001c0001t0016 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(298): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTAA others(419): Show |
1 | a0001c0001t0010 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTTA others(215): Show |
1 | a0001c0001t0022 | 2 | HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(216): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTTA others(517): Show |
1 | a0001c0001t0006 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(518): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTTA others(355): Show |
1 | a0001c0001t0010 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(356): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088071 | C | CGTATTTA others(395): Show |
1 | a0001c0001t0016 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(396): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | ||||||
| chrX:85088072 | A | G | 16 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(13): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088072 | ||||||
| chrX:85088072 | A | T | 16 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0011 others(13): Show |
33 | HG00558.hp1 HG00673.hp1 HG01515.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088072 | ||||||
| chrX:85088073 | T | TATTA | 16 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(13): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*397_*398insTAAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 398 | INFO_REALIGN_3_PRIME | chrX | 85088073 | |||||
| chrX:85088075 | T | C | 1 | a0001c0001t0016 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 397 | chrX | 85088075 | ||||||
| chrX:85088077 | C | T | 1 | a0001c0001t0016 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 399 | chrX | 85088077 | ||||||
| chrX:85088093 | CAT | C | 19 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(16): Show |
42 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*420delTA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088093 | |||||
| chrX:85088095 | T | TACATATT others(263): Show |
1 | a0001c0001t0052 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418_*419insCATATT others(264): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088095 | |||||
| chrX:85088095 | T | TACATATT others(387): Show |
1 | a0001c0001t0024 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418_*419insCATATT others(388): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088095 | |||||
| chrX:85088095 | T | TACATATT others(195): Show |
1 | a0001c0001t0040 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418_*419insCATATT others(196): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088095 | |||||
| chrX:85088095 | T | TACATATT others(255): Show |
1 | a0001c0001t0041 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418_*419insCATATT others(256): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088095 | |||||
| chrX:85088100 | A | G | 2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*422A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 422 | chrX | 85088100 | ||||||
| chrX:85088104 | T | TTATACAT others(15): Show |
2 | a0001c0001t0011 a0001c0001t0068 |
2 | NA18993.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*429_*450dupTACATA others(16): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088104 | |||||
| chrX:85088109 | C | CAT | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(11): Show |
32 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437dupAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 438 | INFO_REALIGN_3_PRIME | chrX | 85088109 | |||||
| chrX:85088125 | C | CAT | 7 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0016 others(4): Show |
13 | HG02055.hp1 HG02145.hp1 HG02622.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*449_*450dupTA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088125 | |||||
| chrX:85088125 | C | CATATACA others(17): Show |
2 | a0001c0001t0011 a0001c0001t0048 |
4 | HG00673.hp1 HG03041.hp1 NA18964.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451insTACATA others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088125 | |||||
| chrX:85088125 | C | CATATACA others(49): Show |
2 | a0001c0001t0025 a0001c0001t0054 |
3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*450_*451insTACATA others(50): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088125 | |||||
| chrX:85088129 | C | A | 1 | a0001c0001t0093 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*451C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | chrX | 85088129 | ||||||
| chrX:85088130 | A | G | 4 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0050 others(1): Show |
4 | HG02109.hp1 HG02559.hp1 NA18981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*452A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 452 | chrX | 85088130 | ||||||
| chrX:85088134 | T | TTATACAT others(17): Show |
1 | a0001c0001t0052 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467_*468insATGTAT others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 468 | INFO_REALIGN_3_PRIME | chrX | 85088134 | |||||
| chrX:85088139 | C | CAT | 15 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(12): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*466_*467dupAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 468 | INFO_REALIGN_3_PRIME | chrX | 85088139 | |||||
| chrX:85088141 | TATATGTA others(21): Show |
T | 2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*468_*495delGTATAA others(22): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 468 | INFO_REALIGN_3_PRIME | chrX | 85088141 | |||||
| chrX:85088155 | C | CAT | 4 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0022 others(1): Show |
5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*479_*480dupTA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATACATA others(219): Show |
2 | a0001c0001t0004 a0001c0001t0044 |
2 | HG01884.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(220): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATACATA others(187): Show |
6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0015 others(3): Show |
20 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(188): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATACATA others(155): Show |
2 | a0001c0001t0015 a0002c0002t0007 |
2 | HG00738.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(156): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATACATA others(155): Show |
1 | a0001c0001t0014 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(156): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATACATA others(155): Show |
1 | a0001c0001t0014 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(156): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATACATA others(155): Show |
1 | a0001c0001t0014 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(156): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATATACA others(17): Show |
3 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0051 |
6 | HG02055.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*480_*481insTACATA others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATATACA others(39): Show |
1 | a0001c0001t0021 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480_*481insTACATA others(40): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATATACA others(61): Show |
1 | a0001c0001t0021 | 2 | HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*480_*481insTACATA others(62): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088155 | C | CATATTTA others(339): Show |
1 | a0001c0001t0050 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480_*481insTTTATA others(340): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | |||||
| chrX:85088160 | A | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(23): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*482A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 482 | chrX | 85088160 | ||||||
| chrX:85088165 | T | A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*487T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 487 | chrX | 85088165 | ||||||
| chrX:85088169 | C | CAT | 11 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0040 others(8): Show |
18 | HG00558.hp1 HG01515.hp1 HG01517.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*496_*497dupAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088169 | |||||
| chrX:85088169 | C | CATATATA others(59): Show |
1 | a0001c0001t0036 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(60): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088169 | |||||
| chrX:85088169 | C | CATATATA others(23): Show |
1 | a0001c0001t0099 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(24): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088169 | |||||
| chrX:85088169 | C | CATATATG others(25): Show |
31 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0034 others(28): Show |
35 | HG01074.hp1 HG01106.hp1 HG01175.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*527_*558dupTATGTA others(26): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 559 | INFO_REALIGN_3_PRIME | chrX | 85088169 | |||||
| chrX:85088169 | C | CATATATG others(57): Show |
6 | a0001c0001t0062 a0001c0001t0069 a0001c0001t0079 others(3): Show |
6 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*495_*558dupTATGTA others(58): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 559 | INFO_REALIGN_3_PRIME | chrX | 85088169 | |||||
| chrX:85088169 | C | CATATATG others(89): Show |
1 | a0001c0001t0095 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558_*559insTATGTA others(90): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 559 | INFO_REALIGN_3_PRIME | chrX | 85088169 | |||||
| chrX:85088169 | C | CATATATG others(55): Show |
2 | a0001c0001t0070 a0001c0001t0074 |
2 | HG01168.hp2 NA18959.hp1 |
3_prime_UTR_variant | MODIFIER | c.*527_*528insGTATAA others(56): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 528 | INFO_REALIGN_3_PRIME | chrX | 85088169 | |||||
| chrX:85088169 | C | CATATATG others(87): Show |
1 | a0001c0001t0101 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527_*528insGTATAA others(88): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 528 | INFO_REALIGN_3_PRIME | chrX | 85088169 | |||||
| chrX:85088181 | AATAC | A | 2 | a0001c0001t0025 a0001c0001t0054 |
3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*511_*514delCATA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 511 | INFO_REALIGN_3_PRIME | chrX | 85088181 | |||||
| chrX:85088190 | A | ATATTTAT others(99): Show |
1 | a0001c0001t0040 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542_*543insTACATA others(100): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 543 | INFO_REALIGN_3_PRIME | chrX | 85088190 | |||||
| chrX:85088190 | A | ATATTTAT others(127): Show |
1 | a0001c0001t0041 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*542_*543insTACATA others(128): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 543 | INFO_REALIGN_3_PRIME | chrX | 85088190 | |||||
| chrX:85088190 | A | G | 3 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0100 |
3 | HG02109.hp1 HG02559.hp1 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*512A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 512 | chrX | 85088190 | ||||||
| chrX:85088199 | CAT | C | 4 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0022 others(1): Show |
10 | HG00673.hp1 HG02622.hp1 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*528_*529delAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 528 | INFO_REALIGN_3_PRIME | chrX | 85088199 | |||||
| chrX:85088206 | A | G | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*528A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 528 | chrX | 85088206 | ||||||
| chrX:85088207 | TGTATAA | T | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*530_*535delGTATAA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 530 | chrX | 85088207 | ||||||
| chrX:85088222 | A | G | 3 | a0001c0001t0031 a0001c0001t0038 a0001c0001t0039 |
4 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*544A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 544 | chrX | 85088222 | ||||||
| chrX:85088316 | G | GT | 20 | a0001c0001t0024 a0001c0001t0025 a0001c0001t0042 others(17): Show |
22 | HG00438.hp1 HG00735.hp1 HG01106.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*667dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | G | GTT | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(11): Show |
32 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*666_*667dupTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | G | GTTT | 6 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0015 others(3): Show |
14 | HG00738.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*665_*667dupTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | G | GTTTT | 2 | a0001c0001t0003 a0001c0001t0052 |
16 | HG01099.hp1 HG02165.hp2 HG03139.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*664_*667dupTTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | G | GTTTTT | 5 | a0001c0001t0001 a0001c0001t0026 a0001c0001t0027 others(2): Show |
43 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*663_*667dupTTTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | G | GTTTTTT | 7 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0019 others(4): Show |
40 | HG00280.hp1 HG00735.hp2 HG01168.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*667dupTTTTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | G | GTTTTTTT | 2 | a0001c0001t0005 a0001c0001t0060 |
10 | HG00609.hp1 HG01123.hp1 HG01361.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*661_*667dupTTTTTT others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | G | GTTTTTTT others(1): Show |
4 | a0001c0001t0009 a0001c0001t0020 a0001c0001t0030 others(1): Show |
11 | HG01884.hp1 HG01978.hp2 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*660_*667dupTTTTTT others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | GTTTTTTT | G | 2 | a0001c0001t0017 a0001c0001t0031 |
5 | HG02257.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*661_*667delTTTTTT others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 661 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088316 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0021 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*656_*667delTTTTTT others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 656 | INFO_REALIGN_3_PRIME | chrX | 85088316 | |||||
| chrX:85088817 | CAGTGAGC others(42): Show |
C | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
175 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1140_*1188delAGTG others(45): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1140 | chrX | 85088817 | ||||||
| chrX:85088890 | A | G | 1 | a0001c0001t0014 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1212A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1212 | chrX | 85088890 | ||||||
| chrX:85088988 | C | T | 1 | a0001c0001t0021 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1310C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1310 | chrX | 85088988 | ||||||
| chrX:85089148 | C | T | 1 | a0001c0001t0053 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1470C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1470 | chrX | 85089148 | ||||||
| chrX:85089243 | A | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(23): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1565A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1565 | chrX | 85089243 | ||||||
| chrX:85089349 | C | T | 1 | a0001c0001t0045 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1671 | chrX | 85089349 | ||||||
| chrX:85089658 | C | T | 2 | a0001c0001t0004 a0001c0001t0042 |
11 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1980C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1980 | chrX | 85089658 | ||||||
| chrX:85089713 | A | T | 1 | a0001c0001t0023 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2035A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2035 | chrX | 85089713 | ||||||
| chrX:85089732 | A | G | 15 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(12): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2054A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2054 | chrX | 85089732 | ||||||
| chrX:85089757 | GTC | G | 1 | a0001c0001t0019 | 3 | HG01255.hp1 HG02602.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2083_*2084delCT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2083 | INFO_REALIGN_3_PRIME | chrX | 85089757 | |||||
| chrX:85089765 | C | T | 1 | a0001c0001t0087 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2087 | chrX | 85089765 | ||||||
| chrX:85089966 | C | CA | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(32): Show |
148 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*2303dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2304 | INFO_REALIGN_3_PRIME | chrX | 85089966 | |||||
| chrX:85090053 | A | G | 1 | a0001c0001t0034 | 2 | NA18954.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2375A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2375 | chrX | 85090053 | ||||||
| chrX:85090702 | C | T | 1 | a0001c0001t0021 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3024C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3024 | chrX | 85090702 | ||||||
| chrX:85090859 | G | C | 4 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0023 others(1): Show |
11 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3181G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3181 | chrX | 85090859 | ||||||
| chrX:85091058 | A | G | 1 | a0001c0001t0056 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3380A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3380 | chrX | 85091058 | ||||||
| chrX:85091205 | G | A | 1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3527G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3527 | chrX | 85091205 | ||||||
| chrX:85091282 | A | G | 1 | a0001c0001t0059 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3604A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3604 | chrX | 85091282 | ||||||
| chrX:85091445 | A | G | 1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3767A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3767 | chrX | 85091445 | ||||||
| chrX:85091474 | T | C | 3 | a0001c0001t0009 a0001c0001t0018 a0001c0001t0060 |
9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3796T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3796 | chrX | 85091474 | ||||||
| chrX:85091603 | C | T | 1 | a0001c0001t0051 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3925C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3925 | chrX | 85091603 | ||||||
| chrX:85091623 | A | T | 16 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(13): Show |
36 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3945A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3945 | chrX | 85091623 | ||||||
| chrX:85091727 | C | G | 3 | a0001c0001t0008 a0001c0001t0030 a0001c0001t0061 |
8 | HG02040.hp1 NA18948.hp1 NA18954.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4049C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4049 | chrX | 85091727 | ||||||
| chrX:85091810 | A | G | 1 | a0001c0001t0022 | 2 | HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4132A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4132 | chrX | 85091810 | ||||||
| chrX:85091919 | T | G | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(13): Show |
113 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*4241T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4241 | chrX | 85091919 | ||||||
| chrX:85091964 | T | G | 1 | a0001c0001t0026 | 2 | HG02615.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4286T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4286 | chrX | 85091964 | ||||||
| chrX:85092348 | A | G | 1 | a0001c0001t0039 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4670A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4670 | chrX | 85092348 | ||||||
| chrX:85093005 | A | G | 1 | a0001c0001t0028 | 2 | HG03017.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5327A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 5327 | chrX | 85093005 | ||||||
| chrX:85093129 | ATATT | A | 10 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(7): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5456_*5459delTATT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 5456 | INFO_REALIGN_3_PRIME | chrX | 85093129 |
| 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:85004088 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.15+161C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004088 | |||||||
| chrX:85004582 | G | T | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+655G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004582 | |||||||
| chrX:85004693 | T | C | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+766T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004693 | |||||||
| chrX:85004771 | C | T | 12 | a0001c0001t0007g0236 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+844C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004771 | |||||||
| chrX:85004808 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.15+881C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004808 | |||||||
| chrX:85004845 | C | T | 1 | a0001c0001t0074g0233 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.15+918C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004845 | |||||||
| chrX:85005020 | T | C | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+1093T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005020 | |||||||
| chrX:85005144 | A | ATTTTATT | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+1228_15+1234dup others(7): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005144 | ||||||
| chrX:85005184 | C | T | 2 | a0001c0001t0006g0210 a0001c0001t0006g0211 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.15+1257C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005184 | |||||||
| chrX:85005289 | G | A | 12 | a0001c0001t0007g0236 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+1362G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005289 | |||||||
| chrX:85005372 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+1445C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005372 | |||||||
| chrX:85005394 | A | AC | 62 | a0001c0001t0001g0165 a0001c0001t0001g0169 a0001c0001t0001g0170 others(59): Show |
62 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+1482dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | A | ACC | 56 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
57 | HG00438.hp2 HG00735.hp1 HG01169.hp2 others(54): Show |
intron_variant | MODIFIER | c.15+1481_15+1482dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | A | ACCC | 24 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(21): Show |
24 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.15+1480_15+1482dup others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | A | ACCCC | 15 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0246 others(12): Show |
15 | HG00280.hp1 HG01071.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.15+1479_15+1482dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | A | ACG | 17 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.15+1468_15+1469ins others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | A | ACGCCCCC others(3): Show |
1 | a0001c0001t0051g0221 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | A | ACGCCCCC others(4): Show |
1 | a0001c0001t0010g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | A | ACGCCCCC others(5): Show |
1 | a0001c0001t0016g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(12): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | A | ACGCCCCC others(6): Show |
1 | a0001c0001t0048g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(13): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005394 | AC | A | 17 | a0001c0001t0001g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(14): Show |
20 | HG00438.hp1 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.15+1482delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | ||||||
| chrX:85005404 | C | T | 11 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(8): Show |
11 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+1477C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005404 | |||||||
| chrX:85005675 | T | TGAATAAA others(19): Show |
4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1752_15+1777dup others(26): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005675 | ||||||
| chrX:85005735 | AAC | A | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.15+1812_15+1813del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005735 | ||||||
| chrX:85005819 | C | T | 8 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0209 others(5): Show |
8 | NA18960.hp1 NA18968.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+1892C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005819 | |||||||
| chrX:85005899 | C | A | 1 | a0001c0001t0004g0222 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.15+1972C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005899 | |||||||
| chrX:85006053 | C | T | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+2126C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006053 | |||||||
| chrX:85006289 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+2362A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006289 | |||||||
| chrX:85006334 | GA | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+2408delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006334 | |||||||
| chrX:85006343 | A | G | 2 | a0001c0001t0003g0157 a0001c0001t0020g0188 |
2 | NA19001.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.15+2416A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006343 | |||||||
| chrX:85006557 | T | TA | 4 | a0001c0001t0026g0161 a0001c0001t0026g0190 a0001c0001t0027g0008 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+2644dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85006557 | ||||||
| chrX:85006639 | A | G | 3 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 |
3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.15+2712A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006639 | |||||||
| chrX:85006822 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(129): Show |
133 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.15+2895A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006822 | |||||||
| chrX:85007181 | T | C | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+3254T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007181 | |||||||
| chrX:85007222 | G | T | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+3295G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007222 | |||||||
| chrX:85007622 | T | C | 2 | a0001c0001t0012g0117 a0001c0001t0012g0162 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.15+3695T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007622 | |||||||
| chrX:85007650 | C | T | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+3723C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007650 | |||||||
| chrX:85007802 | C | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+3875C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007802 | |||||||
| chrX:85007882 | T | C | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+3955T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007882 | |||||||
| chrX:85008013 | A | G | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.15+4086A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008013 | |||||||
| chrX:85008315 | C | G | 2 | a0001c0001t0031g0113 a0001c0001t0031g0156 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.15+4388C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008315 | |||||||
| chrX:85008411 | A | G | 2 | a0001c0001t0010g0017 a0001c0001t0010g0024 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.15+4484A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008411 | |||||||
| chrX:85008534 | G | GT | 9 | a0001c0001t0004g0222 a0001c0001t0004g0225 a0001c0001t0004g0226 others(6): Show |
9 | HG01081.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+4609dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008534 | ||||||
| chrX:85008535 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0003g0118 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.15+4608_15+4609ins others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008535 | |||||||
| chrX:85008535 | T | TTG | 5 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0010g0024 others(2): Show |
5 | HG00733.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+4646_15+4647dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTG | 8 | a0001c0001t0016g0219 a0001c0001t0022g0009 a0001c0001t0025g0013 others(5): Show |
9 | HG00735.hp1 HG01346.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4644_15+4647dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTG | 11 | a0001c0001t0001g0095 a0001c0001t0001g0165 a0001c0001t0010g0220 others(8): Show |
11 | HG00558.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+4642_15+4647dup others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTGT others(1): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0096 others(13): Show |
17 | HG01175.hp2 HG01243.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.15+4640_15+4647dup others(8): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTGT others(3): Show |
35 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0101 others(32): Show |
36 | HG00642.hp1 HG01192.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.15+4638_15+4647dup others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTGT others(5): Show |
41 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0001g0105 others(38): Show |
41 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.15+4636_15+4647dup others(12): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTGT others(7): Show |
22 | a0001c0001t0001g0109 a0001c0001t0001g0183 a0001c0001t0001g0203 others(19): Show |
22 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.15+4634_15+4647dup others(14): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTGT others(9): Show |
5 | a0001c0001t0008g0150 a0001c0001t0008g0186 a0001c0001t0009g0094 others(2): Show |
5 | HG02004.hp1 HG02602.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+4632_15+4647dup others(16): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTGT others(11): Show |
2 | a0001c0001t0030g0152 a0001c0001t0061g0187 |
2 | NA18965.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.15+4630_15+4647dup others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTGT others(13): Show |
2 | a0001c0001t0008g0154 a0001c0001t0030g0153 |
2 | NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.15+4628_15+4647dup others(20): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTGTGTGT others(15): Show |
3 | a0001c0001t0008g0155 a0001c0001t0031g0113 a0001c0001t0031g0156 |
3 | HG02257.hp1 HG03195.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.15+4626_15+4647dup others(22): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTTGTG | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0216 |
3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.15+4609_15+4610ins others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTTGTGTG | 10 | a0001c0001t0007g0236 a0001c0001t0007g0240 a0001c0001t0007g0241 others(7): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+4609_15+4610ins others(7): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTTGTGTG others(4): Show |
1 | a0002c0002t0007g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.15+4609_15+4610ins others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | T | TTTGTGTG others(6): Show |
1 | a0001c0001t0007g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.15+4609_15+4610ins others(13): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008535 | TTG | T | 5 | a0001c0001t0004g0223 a0001c0001t0038g0022 a0001c0001t0039g0023 others(2): Show |
5 | HG01168.hp2 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+4646_15+4647del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | ||||||
| chrX:85008575 | A | G | 2 | a0001c0001t0019g0151 a0001c0001t0019g0181 |
2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.15+4648A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008575 | |||||||
| chrX:85008608 | C | T | 6 | a0001c0001t0002g0091 a0001c0001t0002g0146 a0001c0001t0005g0112 others(3): Show |
6 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+4681C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008608 | |||||||
| chrX:85009378 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.15+5451A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009378 | |||||||
| chrX:85009592 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.15+5665A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009592 | |||||||
| chrX:85009605 | A | G | 3 | a0001c0001t0013g0007 a0001c0001t0013g0185 a0001c0001t0055g0007 |
3 | HG02922.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.15+5678A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009605 | |||||||
| chrX:85009702 | G | A | 1 | a0001c0001t0048g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+5775G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009702 | |||||||
| chrX:85009816 | G | A | 2 | a0001c0001t0012g0117 a0001c0001t0012g0162 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.15+5889G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009816 | |||||||
| chrX:85009892 | A | G | 2 | a0001c0001t0006g0070 a0001c0001t0006g0071 |
2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.15+5965A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009892 | |||||||
| chrX:85009918 | C | T | 2 | a0001c0001t0031g0113 a0001c0001t0031g0156 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.15+5991C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009918 | |||||||
| chrX:85009976 | A | G | 1 | a0001c0001t0056g0145 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.15+6049A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009976 | |||||||
| chrX:85010218 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.15+6291T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010218 | |||||||
| chrX:85010299 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+6372C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010299 | |||||||
| chrX:85010309 | T | C | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+6382T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010309 | |||||||
| chrX:85010360 | A | C | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+6433A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010360 | |||||||
| chrX:85010436 | T | C | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+6509T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010436 | |||||||
| chrX:85010600 | T | C | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6673T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010600 | |||||||
| chrX:85011109 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18940.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.15+7182T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011109 | |||||||
| chrX:85011168 | A | G | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+7241A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011168 | |||||||
| chrX:85011209 | G | A | 1 | a0001c0001t0094g0026 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.15+7282G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011209 | |||||||
| chrX:85011211 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.15+7284T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011211 | |||||||
| chrX:85011428 | A | T | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+7501A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011428 | |||||||
| chrX:85011443 | G | A | 1 | a0001c0001t0007g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.15+7516G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011443 | |||||||
| chrX:85011552 | C | T | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+7625C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011552 | |||||||
| chrX:85011553 | A | G | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+7626A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011553 | |||||||
| chrX:85011563 | C | T | 1 | a0001c0001t0033g0046 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.15+7636C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011563 | |||||||
| chrX:85011693 | G | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+7766G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011693 | |||||||
| chrX:85012000 | G | C | 1 | a0001c0001t0069g0056 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.15+8073G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012000 | |||||||
| chrX:85012066 | G | A | 3 | a0001c0001t0006g0028 a0001c0001t0006g0057 a0001c0001t0024g0027 |
3 | NA18985.hp1 NA19000.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.15+8139G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012066 | |||||||
| chrX:85012498 | A | G | 6 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(3): Show |
6 | HG02647.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+8571A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012498 | |||||||
| chrX:85012509 | A | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+8582A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012509 | |||||||
| chrX:85012818 | T | G | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+8891T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012818 | |||||||
| chrX:85012964 | A | G | 1 | a0001c0001t0004g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+9037A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012964 | |||||||
| chrX:85013173 | G | A | 5 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0003g0173 others(2): Show |
5 | HG00438.hp2 HG02056.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+9246G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013173 | |||||||
| chrX:85013201 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+9274G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013201 | |||||||
| chrX:85013563 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(185): Show |
191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.15+9636A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013563 | |||||||
| chrX:85013692 | T | A | 1 | a0001c0001t0009g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.15+9765T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013692 | |||||||
| chrX:85013704 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.15+9777T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013704 | |||||||
| chrX:85013951 | T | C | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.15+10024T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013951 | |||||||
| chrX:85013972 | A | G | 1 | a0001c0001t0093g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15+10045A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013972 | |||||||
| chrX:85014165 | C | T | 1 | a0001c0001t0079g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.15+10238C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014165 | |||||||
| chrX:85014333 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+10406T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014333 | |||||||
| chrX:85014529 | A | AT | 10 | a0001c0001t0001g0172 a0001c0001t0006g0028 a0001c0001t0006g0057 others(7): Show |
10 | HG00673.hp1 HG02015.hp1 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+10615dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85014529 | ||||||
| chrX:85014529 | AT | A | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+10615delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85014529 | ||||||
| chrX:85014543 | G | A | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+10616G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014543 | |||||||
| chrX:85014553 | G | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+10626G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014553 | |||||||
| chrX:85014566 | CTTTA | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+10645_15+10648d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85014566 | ||||||
| chrX:85014802 | A | G | 1 | a0001c0001t0009g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+10875A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014802 | |||||||
| chrX:85014842 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.15+10915C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014842 | |||||||
| chrX:85014864 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+10937A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014864 | |||||||
| chrX:85015012 | T | C | 5 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+11085T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015012 | |||||||
| chrX:85015039 | T | G | 1 | a0001c0001t0044g0212 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.15+11112T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015039 | |||||||
| chrX:85015228 | T | A | 8 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0183 others(5): Show |
8 | NA18961.hp1 NA18964.hp1 NA18993.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+11301T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015228 | |||||||
| chrX:85015372 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+11445G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015372 | |||||||
| chrX:85015377 | T | C | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+11450T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015377 | |||||||
| chrX:85015385 | G | A | 1 | a0001c0001t0093g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15+11458G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015385 | |||||||
| chrX:85015542 | A | ATATT | 21 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0179 others(18): Show |
22 | HG00733.hp2 HG01099.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.15+11655_15+11658d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015542 | ||||||
| chrX:85015542 | A | ATATTTAT others(5): Show |
1 | a0001c0001t0059g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.15+11647_15+11658d others(14): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015542 | ||||||
| chrX:85015542 | ATATT | A | 38 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0175 others(35): Show |
38 | HG01081.hp2 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.15+11655_15+11658d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015542 | ||||||
| chrX:85015664 | G | A | 1 | a0001c0001t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.15+11737G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015664 | |||||||
| chrX:85015935 | G | A | 1 | a0001c0001t0007g0240 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15+12008G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015935 | |||||||
| chrX:85016012 | G | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+12085G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016012 | |||||||
| chrX:85016204 | T | C | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+12277T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016204 | |||||||
| chrX:85016208 | A | G | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+12281A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016208 | |||||||
| chrX:85016263 | C | T | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.15+12336C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016263 | |||||||
| chrX:85016652 | AG | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+12726delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016652 | |||||||
| chrX:85016692 | G | A | 1 | a0001c0001t0093g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15+12765G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016692 | |||||||
| chrX:85016871 | C | T | 2 | a0001c0001t0003g0157 a0001c0001t0020g0188 |
2 | NA19001.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.15+12944C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016871 | |||||||
| chrX:85016876 | T | C | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+12949T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016876 | |||||||
| chrX:85016971 | G | T | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13044G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016971 | |||||||
| chrX:85017064 | C | T | 1 | a0001c0001t0093g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15+13137C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017064 | |||||||
| chrX:85017215 | C | T | 4 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(1): Show |
4 | HG02647.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+13288C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017215 | |||||||
| chrX:85017257 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+13330T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017257 | |||||||
| chrX:85017672 | C | T | 9 | a0001c0001t0009g0094 a0001c0001t0009g0193 a0001c0001t0009g0196 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+13745C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017672 | |||||||
| chrX:85017684 | G | A | 3 | a0001c0001t0035g0004 a0001c0001t0080g0025 a0001c0001t0081g0004 |
3 | NA18971.hp1 NA19001.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.15+13757G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017684 | |||||||
| chrX:85017810 | T | C | 1 | a0001c0001t0048g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+13883T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017810 | |||||||
| chrX:85017886 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+13959A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017886 | |||||||
| chrX:85017898 | C | T | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13971C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017898 | |||||||
| chrX:85018246 | G | A | 2 | a0001c0001t0006g0070 a0001c0001t0006g0071 |
2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.15+14319G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85018246 | |||||||
| chrX:85018324 | T | C | 1 | a0001c0001t0010g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.15+14397T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85018324 | |||||||
| chrX:85018353 | G | A | 1 | a0001c0001t0100g0029 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.15+14426G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85018353 | |||||||
| chrX:85018578 | C | CT | 8 | a0001c0001t0010g0017 a0001c0001t0010g0024 a0001c0001t0016g0053 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+14662dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85018578 | ||||||
| chrX:85018942 | GT | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(135): Show |
140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.15+15019delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85018942 | ||||||
| chrX:85019025 | C | T | 1 | a0001c0001t0019g0199 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.15+15098C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019025 | |||||||
| chrX:85019112 | G | A | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+15185G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019112 | |||||||
| chrX:85019216 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(110): Show |
114 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.15+15289A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019216 | |||||||
| chrX:85019219 | T | C | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+15292T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019219 | |||||||
| chrX:85019265 | AT | A | 3 | a0001c0001t0001g0109 a0001c0001t0002g0108 a0001c0001t0002g0110 |
3 | HG00140.hp1 HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.15+15339delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019265 | |||||||
| chrX:85019654 | C | T | 12 | a0001c0001t0007g0236 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+15727C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019654 | |||||||
| chrX:85019694 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.15+15767A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019694 | |||||||
| chrX:85019907 | A | G | 3 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 |
3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.15+15980A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019907 | |||||||
| chrX:85019997 | C | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+16070C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019997 | |||||||
| chrX:85020243 | A | G | 1 | a0001c0001t0052g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.15+16316A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85020243 | |||||||
| chrX:85020292 | G | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+16365G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85020292 | |||||||
| chrX:85020676 | T | C | 29 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(26): Show |
29 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.15+16749T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85020676 | |||||||
| chrX:85020921 | C | T | 11 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(8): Show |
11 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+16994C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85020921 | |||||||
| chrX:85021014 | A | G | 2 | a0001c0001t0057g0141 a0001c0001t0059g0143 |
2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.15+17087A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021014 | |||||||
| chrX:85021065 | A | T | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+17138A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021065 | |||||||
| chrX:85021107 | G | C | 1 | a0001c0001t0016g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.15+17180G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021107 | |||||||
| chrX:85021276 | C | T | 1 | a0001c0001t0021g0074 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+17349C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021276 | |||||||
| chrX:85021477 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(184): Show |
190 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.15+17550G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021477 | |||||||
| chrX:85021644 | GCT | G | 5 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+17719_15+17720d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85021644 | ||||||
| chrX:85021850 | CCTT | C | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+17924_15+17926d others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021850 | |||||||
| chrX:85022229 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(175): Show |
180 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.15+18302T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85022229 | |||||||
| chrX:85022259 | A | C | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+18332A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85022259 | |||||||
| chrX:85022281 | A | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.15+18354A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85022281 | |||||||
| chrX:85022641 | AAAAGCT | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+18724_15+18729d others(8): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85022641 | ||||||
| chrX:85022659 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15+18732C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85022659 | |||||||
| chrX:85023224 | G | C | 4 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG01257.hp2 HG02698.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+19297G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85023224 | |||||||
| chrX:85023327 | A | G | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+19400A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85023327 | |||||||
| chrX:85023619 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+19692A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85023619 | |||||||
| chrX:85023682 | C | T | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+19755C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85023682 | |||||||
| chrX:85024086 | G | T | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+20159G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024086 | |||||||
| chrX:85024229 | T | C | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+20302T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024229 | |||||||
| chrX:85024275 | T | C | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.15+20348T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024275 | |||||||
| chrX:85024313 | T | C | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+20386T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024313 | |||||||
| chrX:85024350 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+20423A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024350 | |||||||
| chrX:85024449 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.15+20522T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024449 | |||||||
| chrX:85024482 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0003g0158 a0001c0001t0003g0189 |
3 | NA18960.hp1 NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.15+20555C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024482 | |||||||
| chrX:85024841 | C | T | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+20914C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024841 | |||||||
| chrX:85024951 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+21024A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024951 | |||||||
| chrX:85025035 | C | T | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.15+21108C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025035 | |||||||
| chrX:85025094 | G | A | 32 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(29): Show |
32 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.15+21167G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025094 | |||||||
| chrX:85025304 | C | T | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-21142C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025304 | |||||||
| chrX:85025577 | C | T | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-20869C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025577 | |||||||
| chrX:85025612 | T | C | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-20834T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025612 | |||||||
| chrX:85025634 | A | G | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-20812A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025634 | |||||||
| chrX:85025987 | C | T | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-20459C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025987 | |||||||
| chrX:85026509 | G | T | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-19937G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026509 | |||||||
| chrX:85026511 | T | G | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-19935T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026511 | |||||||
| chrX:85026658 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.16-19788C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026658 | |||||||
| chrX:85026668 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(166): Show |
171 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.16-19778G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026668 | |||||||
| chrX:85026733 | AG | A | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0216 |
3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.16-19711delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85026733 | ||||||
| chrX:85026772 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.16-19674C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026772 | |||||||
| chrX:85026910 | C | T | 2 | a0001c0001t0031g0113 a0001c0001t0031g0156 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-19536C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026910 | |||||||
| chrX:85027068 | G | A | 1 | a0001c0001t0004g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.16-19378G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027068 | |||||||
| chrX:85027262 | G | A | 7 | a0001c0001t0012g0117 a0001c0001t0012g0121 a0001c0001t0012g0162 others(4): Show |
7 | HG02257.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-19184G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027262 | |||||||
| chrX:85027324 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.16-19122T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027324 | |||||||
| chrX:85027722 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.16-18724T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027722 | |||||||
| chrX:85027884 | A | T | 1 | a0001c0001t0054g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-18562A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027884 | |||||||
| chrX:85028238 | C | T | 8 | a0001c0001t0006g0028 a0001c0001t0006g0057 a0001c0001t0024g0019 others(5): Show |
8 | HG02015.hp1 NA18967.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-18208C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85028238 | |||||||
| chrX:85028406 | G | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-18040G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85028406 | |||||||
| chrX:85028634 | A | AT | 6 | a0001c0001t0004g0224 a0001c0001t0038g0022 a0001c0001t0039g0023 others(3): Show |
6 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-17798dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85028634 | ||||||
| chrX:85028695 | C | G | 4 | a0001c0001t0032g0005 a0001c0001t0065g0083 a0001c0001t0066g0082 others(1): Show |
5 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-17751C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85028695 | |||||||
| chrX:85028740 | ATTCAATG others(2): Show |
A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.16-17703_16-17695d others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85028740 | ||||||
| chrX:85029164 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.16-17282G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029164 | |||||||
| chrX:85029241 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.16-17205A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029241 | |||||||
| chrX:85029558 | A | G | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-16888A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029558 | |||||||
| chrX:85029854 | A | G | 8 | a0001c0001t0001g0097 a0001c0001t0001g0140 a0001c0001t0001g0169 others(5): Show |
8 | HG01934.hp1 NA18944.hp1 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-16592A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029854 | |||||||
| chrX:85029945 | A | T | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-16501A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029945 | |||||||
| chrX:85029970 | G | C | 1 | a0001c0001t0033g0046 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.16-16476G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029970 | |||||||
| chrX:85030155 | GC | G | 4 | a0001c0001t0026g0161 a0001c0001t0026g0190 a0001c0001t0027g0008 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-16290delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85030155 | |||||||
| chrX:85030175 | A | G | 2 | a0001c0001t0012g0121 a0001c0001t0017g0120 |
2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.16-16271A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85030175 | |||||||
| chrX:85030319 | C | T | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-16127C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85030319 | |||||||
| chrX:85030809 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-15637G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85030809 | |||||||
| chrX:85031163 | A | G | 1 | a0001c0001t0018g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.16-15283A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85031163 | |||||||
| chrX:85031456 | A | T | 3 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.16-14990A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85031456 | |||||||
| chrX:85031896 | C | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-14550C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85031896 | |||||||
| chrX:85032122 | T | G | 9 | a0001c0001t0012g0117 a0001c0001t0012g0121 a0001c0001t0012g0162 others(6): Show |
9 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-14324T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032122 | |||||||
| chrX:85032243 | G | A | 4 | a0001c0001t0038g0022 a0001c0001t0039g0023 a0001c0001t0047g0010 others(1): Show |
4 | HG02109.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-14203G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032243 | |||||||
| chrX:85032331 | A | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0146 a0001c0001t0005g0148 others(1): Show |
4 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-14115A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032331 | |||||||
| chrX:85032445 | C | T | 1 | a0001c0001t0009g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.16-14001C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032445 | |||||||
| chrX:85032469 | G | A | 1 | a0001c0001t0013g0185 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-13977G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032469 | |||||||
| chrX:85032470 | C | G | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-13976C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032470 | |||||||
| chrX:85032470 | C | T | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-13976C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032470 | |||||||
| chrX:85032471 | G | A | 7 | a0001c0001t0032g0005 a0001c0001t0065g0083 a0001c0001t0066g0082 others(4): Show |
8 | HG00438.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-13975G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032471 | |||||||
| chrX:85032514 | C | CA | 5 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-13917dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85032514 | ||||||
| chrX:85032589 | T | C | 1 | a0001c0001t0011g0042 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.16-13857T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032589 | |||||||
| chrX:85032599 | A | G | 12 | a0001c0001t0007g0236 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.16-13847A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032599 | |||||||
| chrX:85032917 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-13529A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032917 | |||||||
| chrX:85032967 | A | T | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-13479A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032967 | |||||||
| chrX:85033148 | A | G | 1 | a0001c0001t0010g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.16-13298A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033148 | |||||||
| chrX:85033353 | G | A | 3 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.16-13093G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033353 | |||||||
| chrX:85033384 | G | A | 1 | a0001c0001t0007g0240 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.16-13062G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033384 | |||||||
| chrX:85033500 | A | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-12946A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033500 | |||||||
| chrX:85033669 | T | A | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-12777T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033669 | |||||||
| chrX:85033720 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(185): Show |
191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.16-12726T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033720 | |||||||
| chrX:85033848 | G | T | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-12598G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033848 | |||||||
| chrX:85034177 | TA | T | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.16-12259delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85034177 | ||||||
| chrX:85034421 | A | G | 3 | a0001c0001t0012g0163 a0001c0001t0017g0119 a0001c0001t0017g0191 |
3 | HG02257.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.16-12025A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034421 | |||||||
| chrX:85034424 | G | A | 1 | a0001c0001t0094g0026 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.16-12022G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034424 | |||||||
| chrX:85034458 | G | GT | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-11978dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85034458 | ||||||
| chrX:85034608 | T | C | 1 | a0001c0001t0054g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-11838T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034608 | |||||||
| chrX:85034637 | C | T | 1 | a0001c0001t0052g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16-11809C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034637 | |||||||
| chrX:85034719 | T | A | 1 | a0001c0001t0059g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.16-11727T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034719 | |||||||
| chrX:85034720 | T | A | 1 | a0001c0001t0059g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.16-11726T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034720 | |||||||
| chrX:85035058 | C | G | 15 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(12): Show |
15 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.16-11388C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85035058 | |||||||
| chrX:85035558 | T | A | 37 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(34): Show |
37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-10888T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85035558 | |||||||
| chrX:85036254 | G | T | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-10192G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036254 | |||||||
| chrX:85036271 | C | T | 2 | a0001c0001t0010g0017 a0001c0001t0010g0024 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.16-10175C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036271 | |||||||
| chrX:85036277 | C | G | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-10169C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036277 | |||||||
| chrX:85036545 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-9901A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036545 | |||||||
| chrX:85036723 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-9723T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036723 | |||||||
| chrX:85036821 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(185): Show |
191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.16-9625A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036821 | |||||||
| chrX:85037313 | C | T | 7 | a0001c0001t0012g0117 a0001c0001t0012g0121 a0001c0001t0012g0162 others(4): Show |
7 | HG02257.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-9133C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85037313 | |||||||
| chrX:85037432 | G | A | 1 | a0001c0001t0010g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.16-9014G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85037432 | |||||||
| chrX:85037772 | C | T | 1 | a0001c0001t0004g0222 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.16-8674C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85037772 | |||||||
| chrX:85038224 | C | T | 2 | a0001c0001t0003g0158 a0001c0001t0003g0189 |
2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.16-8222C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85038224 | |||||||
| chrX:85038254 | G | T | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-8192G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85038254 | |||||||
| chrX:85038524 | G | GT | 15 | a0001c0001t0006g0028 a0001c0001t0006g0057 a0001c0001t0006g0210 others(12): Show |
15 | HG01168.hp2 HG01346.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.16-7896dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | G | GTT | 5 | a0001c0001t0024g0027 a0001c0001t0054g0050 a0001c0001t0063g0015 others(2): Show |
5 | HG00735.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-7897_16-7896dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | G | GTTTT | 5 | a0001c0001t0007g0240 a0001c0001t0007g0243 a0001c0001t0015g0242 others(2): Show |
5 | HG01167.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-7899_16-7896dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0016g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.16-7909_16-7896dup others(14): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0016g0054 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.16-7913_16-7896dup others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | G | GTTTTTTT others(13): Show |
1 | a0001c0001t0010g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.16-7915_16-7896dup others(20): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | G | GTTTTTTT others(14): Show |
1 | a0001c0001t0010g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.16-7916_16-7896dup others(21): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | G | GTTTTTTT others(18): Show |
1 | a0001c0001t0010g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.16-7920_16-7896dup others(25): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | G | GTTTTTTT others(28): Show |
1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-7896_16-7895ins others(35): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | GT | G | 6 | a0001c0001t0011g0042 a0001c0001t0022g0009 a0001c0001t0034g0078 others(3): Show |
7 | HG00673.hp1 HG01106.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-7896delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | GTTT | G | 22 | a0001c0001t0001g0131 a0001c0001t0001g0204 a0001c0001t0002g0088 others(19): Show |
22 | HG01081.hp2 HG01175.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.16-7898_16-7896del others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | GTTTT | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(123): Show |
128 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.16-7899_16-7896del others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-7906_16-7896del others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038524 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0032g0005 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.16-7909_16-7896del others(14): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | ||||||
| chrX:85038530 | T | G | 1 | a0001c0001t0006g0070 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.16-7916T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85038530 | |||||||
| chrX:85038914 | G | C | 2 | a0001c0001t0073g0030 a0001c0001t0083g0059 |
2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.16-7532G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85038914 | |||||||
| chrX:85039052 | T | C | 1 | a0001c0001t0097g0066 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.16-7394T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039052 | |||||||
| chrX:85039207 | A | G | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-7239A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039207 | |||||||
| chrX:85039230 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(184): Show |
190 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.16-7216C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039230 | |||||||
| chrX:85039254 | G | A | 1 | a0001c0001t0076g0014 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.16-7192G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039254 | |||||||
| chrX:85039297 | T | C | 37 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(34): Show |
37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-7149T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039297 | |||||||
| chrX:85039520 | C | G | 1 | a0001c0001t0075g0038 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.16-6926C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039520 | |||||||
| chrX:85039580 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-6866T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039580 | |||||||
| chrX:85039828 | C | T | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-6618C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039828 | |||||||
| chrX:85039896 | A | C | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-6550A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039896 | |||||||
| chrX:85039952 | G | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-6494G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039952 | |||||||
| chrX:85039961 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-6485T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039961 | |||||||
| chrX:85040175 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.16-6271A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040175 | |||||||
| chrX:85040210 | A | G | 9 | a0001c0001t0009g0094 a0001c0001t0009g0193 a0001c0001t0009g0196 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-6236A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040210 | |||||||
| chrX:85040224 | C | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-6222C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040224 | |||||||
| chrX:85040459 | G | A | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.16-5987G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040459 | |||||||
| chrX:85040708 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-5738T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040708 | |||||||
| chrX:85040718 | A | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-5728A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040718 | |||||||
| chrX:85040739 | G | A | 4 | a0001c0001t0026g0161 a0001c0001t0026g0190 a0001c0001t0027g0008 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-5707G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040739 | |||||||
| chrX:85040976 | G | A | 3 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 |
3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.16-5470G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040976 | |||||||
| chrX:85041111 | G | C | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-5335G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85041111 | |||||||
| chrX:85041421 | A | T | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-5025A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85041421 | |||||||
| chrX:85041694 | A | G | 1 | a0001c0001t0008g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.16-4752A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85041694 | |||||||
| chrX:85041727 | G | A | 1 | a0001c0001t0005g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.16-4719G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85041727 | |||||||
| chrX:85042034 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-4412T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85042034 | |||||||
| chrX:85042528 | G | A | 8 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-3918G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85042528 | |||||||
| chrX:85042690 | A | G | 2 | a0001c0001t0012g0117 a0001c0001t0012g0162 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.16-3756A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85042690 | |||||||
| chrX:85042934 | G | A | 1 | a0001c0001t0040g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.16-3512G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85042934 | |||||||
| chrX:85043090 | G | A | 1 | a0001c0001t0011g0018 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.16-3356G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043090 | |||||||
| chrX:85043174 | A | T | 37 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(34): Show |
37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-3272A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043174 | |||||||
| chrX:85043232 | C | T | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-3214C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043232 | |||||||
| chrX:85043258 | G | T | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-3188G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043258 | |||||||
| chrX:85043269 | C | T | 37 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(34): Show |
37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-3177C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043269 | |||||||
| chrX:85043331 | G | C | 1 | a0001c0001t0004g0226 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.16-3115G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043331 | |||||||
| chrX:85043410 | A | AT | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.16-3022dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85043410 | ||||||
| chrX:85043410 | AT | A | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-3022delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85043410 | ||||||
| chrX:85043467 | A | C | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-2979A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043467 | |||||||
| chrX:85043679 | C | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.16-2767C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043679 | |||||||
| chrX:85043683 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.16-2763G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043683 | |||||||
| chrX:85043771 | A | C | 1 | a0001c0001t0002g0134 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.16-2675A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043771 | |||||||
| chrX:85043775 | C | T | 2 | a0001c0001t0031g0113 a0001c0001t0031g0156 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-2671C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043775 | |||||||
| chrX:85043800 | A | G | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0216 |
3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.16-2646A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043800 | |||||||
| chrX:85043906 | G | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.16-2540G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043906 | |||||||
| chrX:85043964 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-2482A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043964 | |||||||
| chrX:85044182 | A | G | 8 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0183 others(5): Show |
8 | NA18961.hp1 NA18964.hp1 NA18993.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-2264A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044182 | |||||||
| chrX:85044252 | T | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-2194T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044252 | |||||||
| chrX:85044254 | A | ATG | 101 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): Show |
103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.16-2176_16-2175dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044254 | ||||||
| chrX:85044254 | A | ATGTG | 4 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG01257.hp2 HG02698.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2178_16-2175dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044254 | ||||||
| chrX:85044270 | G | GTGTA | 32 | a0001c0001t0001g0097 a0001c0001t0001g0114 a0001c0001t0001g0116 others(29): Show |
32 | HG00609.hp1 HG01934.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.16-2175_16-2174ins others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044270 | ||||||
| chrX:85044272 | A | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-2174A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044272 | |||||||
| chrX:85044356 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(180): Show |
185 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.16-2090G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044356 | |||||||
| chrX:85044515 | A | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.16-1931A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044515 | |||||||
| chrX:85044605 | G | C | 1 | a0001c0001t0063g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.16-1841G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044605 | |||||||
| chrX:85044635 | G | A | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-1811G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044635 | |||||||
| chrX:85044851 | T | A | 1 | a0001c0001t0082g0060 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.16-1595T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044851 | |||||||
| chrX:85045230 | C | T | 3 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.16-1216C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85045230 | |||||||
| chrX:85045592 | T | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-854T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85045592 | |||||||
| chrX:85045836 | G | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0168 |
3 | NA18961.hp1 NA19082.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.16-610G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85045836 | |||||||
| chrX:85045932 | C | T | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-514C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85045932 | |||||||
| chrX:85046008 | A | G | 9 | a0001c0001t0012g0117 a0001c0001t0012g0121 a0001c0001t0012g0162 others(6): Show |
9 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-438A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85046008 | |||||||
| chrX:85046077 | A | G | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-369A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85046077 | |||||||
| chrX:85046793 | G | C | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.120+243G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85046793 | |||||||
| chrX:85046962 | A | G | 1 | a0001c0001t0003g0099 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.120+412A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85046962 | |||||||
| chrX:85046965 | G | C | 2 | a0001c0001t0006g0028 a0001c0001t0024g0027 |
2 | NA18985.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.120+415G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85046965 | |||||||
| chrX:85047281 | C | T | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0216 |
3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.120+731C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047281 | |||||||
| chrX:85047328 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.120+778C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047328 | |||||||
| chrX:85047331 | G | A | 1 | a0001c0001t0010g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.120+781G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047331 | |||||||
| chrX:85047377 | T | G | 1 | a0001c0001t0019g0181 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.120+827T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047377 | |||||||
| chrX:85047510 | C | A | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.120+960C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047510 | |||||||
| chrX:85048292 | A | AT | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.120+1748dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85048292 | ||||||
| chrX:85048519 | T | A | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0216 |
3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.120+1969T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85048519 | |||||||
| chrX:85048651 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.120+2101G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85048651 | |||||||
| chrX:85048896 | C | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(178): Show |
184 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.120+2346C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85048896 | |||||||
| chrX:85049055 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.121-2334A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049055 | |||||||
| chrX:85049074 | G | A | 1 | a0001c0001t0029g0136 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.121-2315G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049074 | |||||||
| chrX:85049464 | G | A | 4 | a0001c0001t0003g0085 a0001c0001t0013g0007 a0001c0001t0013g0185 others(1): Show |
4 | HG02922.hp1 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-1925G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049464 | |||||||
| chrX:85049594 | G | A | 1 | a0001c0001t0004g0222 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.121-1795G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049594 | |||||||
| chrX:85049787 | AAAAC | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.121-1586_121-1583d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85049787 | ||||||
| chrX:85049987 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.121-1402C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049987 | |||||||
| chrX:85050129 | TA | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(175): Show |
181 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.121-1256delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85050129 | ||||||
| chrX:85050142 | C | T | 3 | a0001c0001t0009g0197 a0001c0001t0018g0167 a0001c0001t0018g0194 |
3 | HG01243.hp1 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.121-1247C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050142 | |||||||
| chrX:85050264 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(174): Show |
180 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.121-1125G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050264 | |||||||
| chrX:85050266 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.121-1123T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050266 | |||||||
| chrX:85050287 | G | T | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.121-1102G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050287 | |||||||
| chrX:85050606 | C | CA | 8 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0204 others(5): Show |
9 | HG02055.hp1 HG02602.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-767dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85050606 | ||||||
| chrX:85050606 | CA | C | 32 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(29): Show |
32 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.121-767delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85050606 | ||||||
| chrX:85050721 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18940.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.121-668G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050721 | |||||||
| chrX:85050963 | A | G | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.121-426A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050963 | |||||||
| chrX:85051054 | G | A | 1 | a0001c0001t0046g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.121-335G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85051054 | |||||||
| chrX:85051209 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.121-180G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85051209 | |||||||
| chrX:85051374 | A | AT | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.121-9dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85051374 | ||||||
| chrX:85051641 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.240+133T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85051641 | |||||||
| chrX:85051809 | G | A | 1 | a0001c0001t0029g0107 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.240+301G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85051809 | |||||||
| chrX:85052000 | A | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.240+492A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052000 | |||||||
| chrX:85052251 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.240+743C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052251 | |||||||
| chrX:85052800 | A | G | 29 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(26): Show |
29 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.240+1292A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052800 | |||||||
| chrX:85052945 | C | A | 1 | a0001c0001t0004g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241-1399C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052945 | |||||||
| chrX:85053105 | G | A | 4 | a0001c0001t0026g0161 a0001c0001t0026g0190 a0001c0001t0027g0008 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-1239G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053105 | |||||||
| chrX:85053208 | A | T | 1 | a0001c0001t0079g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.241-1136A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053208 | |||||||
| chrX:85053346 | G | A | 1 | a0001c0001t0044g0212 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.241-998G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053346 | |||||||
| chrX:85053452 | A | T | 1 | a0001c0001t0065g0083 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.241-892A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053452 | |||||||
| chrX:85053950 | C | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.241-394C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053950 | |||||||
| chrX:85054211 | G | A | 1 | a0001c0001t0029g0136 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.241-133G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85054211 | |||||||
| chrX:85054249 | A | G | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.241-95A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85054249 | |||||||
| chrX:85054426 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.295+28T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85054426 | |||||||
| chrX:85054543 | TATTG | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.295+149_295+152del others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 85054543 | ||||||
| chrX:85054951 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.295+553G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85054951 | |||||||
| chrX:85055011 | C | T | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.295+613C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85055011 | |||||||
| chrX:85055319 | G | A | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-508G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85055319 | |||||||
| chrX:85055623 | G | A | 1 | a0001c0001t0015g0235 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.296-204G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85055623 | |||||||
| chrX:85055932 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
splice_region_variant&intron_variant | LOW | c.394+7T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85055932 | |||||||
| chrX:85056175 | A | G | 1 | a0001c0001t0044g0212 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.394+250A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056175 | |||||||
| chrX:85056235 | A | G | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+310A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056235 | |||||||
| chrX:85056355 | T | G | 29 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(26): Show |
29 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.394+430T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056355 | |||||||
| chrX:85056534 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18940.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.394+609G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056534 | |||||||
| chrX:85056789 | T | C | 16 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(13): Show |
16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+864T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056789 | |||||||
| chrX:85056821 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.394+896T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056821 | |||||||
| chrX:85056926 | A | G | 2 | a0001c0001t0031g0113 a0001c0001t0031g0156 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.394+1001A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056926 | |||||||
| chrX:85057094 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.394+1169G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057094 | |||||||
| chrX:85057148 | AT | A | 16 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(13): Show |
16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+1225delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85057148 | ||||||
| chrX:85057183 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+1258G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057183 | |||||||
| chrX:85057387 | C | T | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+1462C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057387 | |||||||
| chrX:85057496 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.394+1571A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057496 | |||||||
| chrX:85057638 | GATATATA others(19): Show |
G | 1 | a0001c0001t0086g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.394+1748_394+1773d others(28): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85057638 | ||||||
| chrX:85057666 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.394+1741T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057666 | |||||||
| chrX:85057701 | A | C | 1 | a0001c0001t0006g0071 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.394+1776A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057701 | |||||||
| chrX:85057949 | G | A | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+2024G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057949 | |||||||
| chrX:85058063 | T | C | 1 | a0001c0001t0056g0145 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.394+2138T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058063 | |||||||
| chrX:85058075 | A | G | 1 | a0001c0001t0079g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.394+2150A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058075 | |||||||
| chrX:85058094 | G | T | 2 | a0001c0001t0006g0070 a0001c0001t0006g0071 |
2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.394+2169G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058094 | |||||||
| chrX:85058096 | T | A | 1 | a0001c0001t0040g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+2171T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058096 | |||||||
| chrX:85058287 | T | C | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.394+2362T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058287 | |||||||
| chrX:85058409 | C | A | 1 | a0001c0001t0006g0058 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.394+2484C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058409 | |||||||
| chrX:85058692 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.394+2767C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058692 | |||||||
| chrX:85058795 | G | C | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+2870G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058795 | |||||||
| chrX:85058944 | G | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.394+3019G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058944 | |||||||
| chrX:85059051 | C | T | 3 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394+3126C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059051 | |||||||
| chrX:85059098 | A | G | 1 | a0001c0001t0052g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394+3173A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059098 | |||||||
| chrX:85059217 | T | G | 4 | a0001c0001t0026g0161 a0001c0001t0026g0190 a0001c0001t0027g0008 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+3292T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059217 | |||||||
| chrX:85059285 | C | T | 1 | a0001c0001t0093g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.394+3360C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059285 | |||||||
| chrX:85059339 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.394+3414C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059339 | |||||||
| chrX:85059415 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.394+3490A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059415 | |||||||
| chrX:85059468 | C | G | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.394+3543C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059468 | |||||||
| chrX:85059587 | G | A | 1 | a0001c0001t0074g0233 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.394+3662G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059587 | |||||||
| chrX:85059648 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.394+3723A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059648 | |||||||
| chrX:85059839 | T | C | 37 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(34): Show |
37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.394+3914T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059839 | |||||||
| chrX:85059925 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(237): Show |
244 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(241): Show |
intron_variant | MODIFIER | c.394+4000T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059925 | |||||||
| chrX:85059933 | G | T | 1 | a0001c0001t0063g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.394+4008G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059933 | |||||||
| chrX:85059974 | T | A | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.394+4049T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059974 | |||||||
| chrX:85060061 | G | A | 1 | a0001c0001t0008g0186 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.394+4136G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060061 | |||||||
| chrX:85060062 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.394+4137T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060062 | |||||||
| chrX:85060129 | T | A | 16 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(13): Show |
16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+4204T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060129 | |||||||
| chrX:85060159 | C | G | 16 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(13): Show |
16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+4234C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060159 | |||||||
| chrX:85060243 | G | C | 1 | a0001c0001t0004g0222 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.394+4318G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060243 | |||||||
| chrX:85060248 | G | T | 8 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.394+4323G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060248 | |||||||
| chrX:85060275 | C | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.394+4350C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060275 | |||||||
| chrX:85060354 | G | A | 1 | a0001c0001t0028g0198 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.394+4429G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060354 | |||||||
| chrX:85060446 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.394+4521T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060446 | |||||||
| chrX:85060459 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.394+4534C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060459 | |||||||
| chrX:85060532 | G | A | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.394+4607G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060532 | |||||||
| chrX:85060538 | A | G | 29 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(26): Show |
29 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.394+4613A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060538 | |||||||
| chrX:85060553 | A | C | 3 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394+4628A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060553 | |||||||
| chrX:85060574 | T | C | 3 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394+4649T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060574 | |||||||
| chrX:85060610 | G | A | 3 | a0001c0001t0038g0022 a0001c0001t0039g0023 a0001c0001t0050g0052 |
3 | HG02109.hp1 HG02559.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.394+4685G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060610 | |||||||
| chrX:85060632 | T | A | 3 | a0001c0001t0034g0078 a0001c0001t0034g0080 a0001c0001t0072g0079 |
3 | HG01358.hp1 NA18954.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.394+4707T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060632 | |||||||
| chrX:85060689 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.394+4764T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060689 | |||||||
| chrX:85060805 | A | G | 1 | a0001c0001t0003g0160 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.394+4880A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060805 | |||||||
| chrX:85060866 | C | T | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+4941C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060866 | |||||||
| chrX:85060954 | G | A | 1 | a0001c0001t0088g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.394+5029G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060954 | |||||||
| chrX:85060954 | G | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(185): Show |
191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.394+5029G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060954 | |||||||
| chrX:85060959 | A | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(185): Show |
191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.394+5034A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060959 | |||||||
| chrX:85061086 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
77 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.394+5161A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061086 | |||||||
| chrX:85061217 | C | A | 2 | a0001c0001t0003g0158 a0001c0001t0003g0189 |
2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.394+5292C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061217 | |||||||
| chrX:85061434 | C | T | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.394+5509C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061434 | |||||||
| chrX:85061435 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.394+5510G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061435 | |||||||
| chrX:85061468 | C | T | 5 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+5543C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061468 | |||||||
| chrX:85061538 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.395-5589G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061538 | |||||||
| chrX:85061590 | T | G | 2 | a0001c0001t0004g0229 a0001c0001t0042g0228 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.395-5537T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061590 | |||||||
| chrX:85061644 | C | T | 1 | a0001c0001t0005g0184 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.395-5483C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061644 | |||||||
| chrX:85061775 | C | G | 1 | a0001c0001t0025g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.395-5352C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061775 | |||||||
| chrX:85061796 | C | G | 9 | a0001c0001t0012g0117 a0001c0001t0012g0121 a0001c0001t0012g0162 others(6): Show |
9 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-5331C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061796 | |||||||
| chrX:85061797 | G | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-5330G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061797 | |||||||
| chrX:85061837 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.395-5290C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061837 | |||||||
| chrX:85061908 | G | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.395-5219G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061908 | |||||||
| chrX:85062116 | T | A | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-5011T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062116 | |||||||
| chrX:85062118 | T | TGCCTTCA others(13): Show |
4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-5008_395-4989d others(22): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85062118 | ||||||
| chrX:85062135 | T | G | 5 | a0001c0001t0002g0134 a0001c0001t0002g0142 a0001c0001t0002g0147 others(2): Show |
5 | HG00609.hp1 HG02027.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-4992T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062135 | |||||||
| chrX:85062297 | A | G | 1 | a0001c0001t0044g0212 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.395-4830A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062297 | |||||||
| chrX:85062315 | C | G | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.395-4812C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062315 | |||||||
| chrX:85062444 | A | G | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4683A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062444 | |||||||
| chrX:85062686 | C | T | 1 | a0001c0001t0053g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.395-4441C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062686 | |||||||
| chrX:85062727 | GT | G | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0216 |
3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.395-4395delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85062727 | ||||||
| chrX:85062788 | G | A | 7 | a0001c0001t0012g0117 a0001c0001t0012g0121 a0001c0001t0012g0162 others(4): Show |
7 | HG02257.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.395-4339G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062788 | |||||||
| chrX:85062853 | G | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(179): Show |
185 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.395-4274G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062853 | |||||||
| chrX:85062914 | C | G | 1 | a0001c0001t0097g0066 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.395-4213C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062914 | |||||||
| chrX:85062935 | T | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.395-4192T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062935 | |||||||
| chrX:85062955 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(186): Show |
192 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.395-4172A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062955 | |||||||
| chrX:85063074 | G | A | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4053G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063074 | |||||||
| chrX:85063120 | C | A | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4007C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063120 | |||||||
| chrX:85063122 | A | G | 1 | a0001c0001t0077g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.395-4005A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063122 | |||||||
| chrX:85063144 | T | A | 1 | a0001c0001t0003g0085 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.395-3983T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063144 | |||||||
| chrX:85063541 | G | A | 1 | a0001c0001t0033g0049 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.395-3586G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063541 | |||||||
| chrX:85063577 | A | T | 1 | a0001c0001t0070g0055 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.395-3550A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063577 | |||||||
| chrX:85063651 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.395-3476C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063651 | |||||||
| chrX:85063652 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.395-3475G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063652 | |||||||
| chrX:85063756 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.395-3371A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063756 | |||||||
| chrX:85063775 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(110): Show |
114 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.395-3352T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063775 | |||||||
| chrX:85063789 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.395-3338G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063789 | |||||||
| chrX:85064081 | A | G | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-3046A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064081 | |||||||
| chrX:85064220 | C | T | 8 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0038g0022 others(5): Show |
8 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-2907C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064220 | |||||||
| chrX:85064339 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.395-2788G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064339 | |||||||
| chrX:85064340 | A | AT | 30 | a0001c0001t0001g0133 a0001c0001t0004g0222 a0001c0001t0004g0223 others(27): Show |
30 | HG00438.hp2 HG01081.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.395-2771dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064340 | ||||||
| chrX:85064340 | A | ATT | 15 | a0001c0001t0007g0236 a0001c0001t0007g0240 a0001c0001t0007g0241 others(12): Show |
15 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.395-2772_395-2771d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064340 | ||||||
| chrX:85064363 | A | AT | 12 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0002g0134 others(9): Show |
12 | HG00438.hp2 HG00609.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.395-2759dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064363 | ||||||
| chrX:85064530 | T | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.395-2597T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064530 | |||||||
| chrX:85064797 | A | C | 9 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0038g0022 others(6): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-2330A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064797 | |||||||
| chrX:85065058 | G | T | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.395-2069G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065058 | |||||||
| chrX:85065103 | T | G | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-2024T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065103 | |||||||
| chrX:85065128 | T | C | 5 | a0001c0001t0002g0111 a0001c0001t0002g0205 a0001c0001t0005g0092 others(2): Show |
5 | HG01261.hp1 HG01361.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-1999T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065128 | |||||||
| chrX:85065240 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.395-1887C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065240 | |||||||
| chrX:85065546 | C | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.395-1581C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065546 | |||||||
| chrX:85065547 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.395-1580G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065547 | |||||||
| chrX:85065553 | G | A | 1 | a0001c0001t0004g0222 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.395-1574G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065553 | |||||||
| chrX:85065625 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(179): Show |
185 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.395-1502G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065625 | |||||||
| chrX:85065934 | G | A | 5 | a0001c0001t0013g0087 a0001c0001t0013g0100 a0001c0001t0019g0151 others(2): Show |
5 | HG01255.hp1 HG02602.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-1193G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065934 | |||||||
| chrX:85065976 | C | T | 9 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.395-1151C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065976 | |||||||
| chrX:85066040 | G | A | 3 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.395-1087G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066040 | |||||||
| chrX:85066092 | A | G | 5 | a0001c0001t0036g0003 a0001c0001t0036g0063 a0001c0001t0062g0072 others(2): Show |
5 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-1035A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066092 | |||||||
| chrX:85066249 | G | A | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.395-878G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066249 | |||||||
| chrX:85066386 | C | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.395-741C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066386 | |||||||
| chrX:85066541 | A | G | 1 | a0001c0001t0057g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.395-586A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066541 | |||||||
| chrX:85066595 | C | T | 1 | a0001c0001t0092g0035 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.395-532C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066595 | |||||||
| chrX:85066638 | T | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-489T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066638 | |||||||
| chrX:85066640 | T | C | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.395-487T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066640 | |||||||
| chrX:85066641 | A | C | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-486A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066641 | |||||||
| chrX:85066642 | C | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-485C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066642 | |||||||
| chrX:85067061 | G | A | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.395-66G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85067061 | |||||||
| chrX:85067109 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.395-18T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85067109 | |||||||
| chrX:85067431 | G | A | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.486+213G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067431 | |||||||
| chrX:85067627 | A | AAAAC | 3 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0003g0115 |
3 | NA19009.hp1 NA19012.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.486+410_486+411ins others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | A | AAC | 89 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0095 others(86): Show |
90 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.486+448_486+449dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | A | AACAC | 20 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0084 others(17): Show |
22 | HG00140.hp1 HG00558.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.486+446_486+449dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | A | AACACAC | 8 | a0001c0001t0002g0146 a0001c0001t0004g0222 a0001c0001t0012g0117 others(5): Show |
8 | HG01169.hp2 HG02818.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+444_486+449dup others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | A | AACACACA others(1): Show |
15 | a0001c0001t0004g0223 a0001c0001t0004g0224 a0001c0001t0004g0226 others(12): Show |
15 | HG01081.hp2 HG01109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.486+442_486+449dup others(8): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | A | AACACACA others(3): Show |
2 | a0001c0001t0004g0232 a0001c0001t0017g0120 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.486+440_486+449dup others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | A | ACAC | 4 | a0001c0001t0001g0105 a0001c0001t0001g0131 a0001c0001t0001g0133 others(1): Show |
4 | HG00438.hp2 HG02698.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+409_486+410ins others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067627 | |||||||
| chrX:85067627 | A | C | 1 | a0001c0001t0015g0235 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486+409A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067627 | |||||||
| chrX:85067627 | AAC | A | 26 | a0001c0001t0001g0101 a0001c0001t0002g0006 a0001c0001t0002g0103 others(23): Show |
26 | HG00642.hp1 HG00738.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.486+448_486+449del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | AACAC | A | 10 | a0001c0001t0010g0017 a0001c0001t0010g0024 a0001c0001t0016g0053 others(7): Show |
10 | HG01346.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+446_486+449del others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | AACACACA others(3): Show |
A | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.486+440_486+449del others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067627 | AACACACA others(11): Show |
A | 1 | a0001c0001t0003g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.486+432_486+449del others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | ||||||
| chrX:85067637 | C | CACACACA others(31): Show |
1 | a0001c0001t0010g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.486+449_486+450ins others(38): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067637 | ||||||
| chrX:85067637 | C | CACACACA others(29): Show |
3 | a0001c0001t0016g0219 a0001c0001t0048g0218 a0001c0001t0051g0221 |
3 | HG02055.hp1 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.486+449_486+450ins others(36): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067637 | ||||||
| chrX:85067639 | C | CACACACA others(17): Show |
1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486+444_486+445ins others(24): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067639 | ||||||
| chrX:85067738 | C | A | 7 | a0001c0001t0008g0150 a0001c0001t0008g0154 a0001c0001t0008g0155 others(4): Show |
7 | NA18948.hp1 NA18954.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+520C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067738 | |||||||
| chrX:85067982 | C | T | 1 | a0001c0001t0063g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.486+764C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067982 | |||||||
| chrX:85068298 | C | T | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.486+1080C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068298 | |||||||
| chrX:85068334 | G | A | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+1116G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068334 | |||||||
| chrX:85068396 | C | CT | 6 | a0001c0001t0003g0118 a0001c0001t0005g0135 a0001c0001t0010g0220 others(3): Show |
6 | HG02027.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+1193dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85068396 | ||||||
| chrX:85068625 | C | T | 1 | a0001c0001t0040g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.486+1407C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068625 | |||||||
| chrX:85068632 | CT | C | 8 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.486+1415delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068632 | |||||||
| chrX:85068653 | G | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486+1435G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068653 | |||||||
| chrX:85068829 | T | A | 9 | a0001c0001t0009g0094 a0001c0001t0009g0193 a0001c0001t0009g0196 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+1611T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068829 | |||||||
| chrX:85068904 | T | C | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.486+1686T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068904 | |||||||
| chrX:85069417 | A | G | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.486+2199A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85069417 | |||||||
| chrX:85069522 | A | C | 1 | a0001c0001t0089g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2304A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85069522 | |||||||
| chrX:85069610 | T | TA | 48 | a0001c0001t0001g0132 a0001c0001t0001g0170 a0001c0001t0001g0179 others(45): Show |
49 | HG00621.hp1 HG00733.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.486+2419dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069610 | ||||||
| chrX:85069610 | T | TAA | 8 | a0001c0001t0004g0227 a0001c0001t0007g0236 a0001c0001t0015g0242 others(5): Show |
9 | HG01169.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+2418_486+2419d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069610 | ||||||
| chrX:85069610 | TA | T | 15 | a0001c0001t0001g0140 a0001c0001t0016g0219 a0001c0001t0021g0048 others(12): Show |
15 | HG01256.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.486+2419delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069610 | ||||||
| chrX:85069812 | T | C | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+2594T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85069812 | |||||||
| chrX:85069929 | C | T | 1 | a0001c0001t0028g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.486+2711C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85069929 | |||||||
| chrX:85070177 | A | T | 2 | a0001c0001t0034g0078 a0001c0001t0034g0080 |
2 | NA18954.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.486+2959A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070177 | |||||||
| chrX:85070361 | T | C | 1 | a0001c0001t0095g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.486+3143T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070361 | |||||||
| chrX:85070466 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(156): Show |
162 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.486+3248G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070466 | |||||||
| chrX:85070504 | C | T | 3 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 |
3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.486+3286C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070504 | |||||||
| chrX:85070559 | T | A | 3 | a0001c0001t0038g0022 a0001c0001t0039g0023 a0001c0001t0050g0052 |
3 | HG02109.hp1 HG02559.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.486+3341T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070559 | |||||||
| chrX:85070615 | A | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.487-3383A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070615 | |||||||
| chrX:85070685 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.487-3313C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070685 | |||||||
| chrX:85070810 | G | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.487-3188G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070810 | |||||||
| chrX:85070819 | C | CA | 14 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0209 others(11): Show |
14 | HG01255.hp1 HG02738.hp1 HG04204.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-3165dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070819 | ||||||
| chrX:85070820 | A | C | 1 | a0001c0001t0089g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.487-3178A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070820 | |||||||
| chrX:85071121 | A | G | 1 | a0001c0001t0033g0049 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.487-2877A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071121 | |||||||
| chrX:85071138 | G | A | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.487-2860G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071138 | |||||||
| chrX:85071223 | A | G | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-2775A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071223 | |||||||
| chrX:85071353 | T | C | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487-2645T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071353 | |||||||
| chrX:85071416 | G | A | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.487-2582G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071416 | |||||||
| chrX:85071620 | C | A | 34 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(31): Show |
34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.487-2378C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071620 | |||||||
| chrX:85071666 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.487-2332T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071666 | |||||||
| chrX:85072581 | C | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
76 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.487-1417C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072581 | |||||||
| chrX:85072615 | G | A | 1 | a0001c0001t0067g0081 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.487-1383G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072615 | |||||||
| chrX:85072717 | A | G | 22 | a0001c0001t0006g0028 a0001c0001t0006g0057 a0001c0001t0024g0019 others(19): Show |
22 | HG00621.hp1 HG02004.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.487-1281A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072717 | |||||||
| chrX:85072895 | A | C | 8 | a0001c0001t0008g0150 a0001c0001t0008g0154 a0001c0001t0008g0155 others(5): Show |
8 | HG02040.hp1 NA18948.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-1103A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072895 | |||||||
| chrX:85072935 | G | A | 9 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.487-1063G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072935 | |||||||
| chrX:85072945 | C | T | 1 | a0001c0001t0072g0079 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.487-1053C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072945 | |||||||
| chrX:85072965 | T | C | 5 | a0001c0001t0025g0013 a0001c0001t0025g0021 a0001c0001t0054g0050 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1033T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072965 | |||||||
| chrX:85073247 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(169): Show |
174 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.487-751T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073247 | |||||||
| chrX:85073377 | A | T | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0216 |
3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.487-621A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073377 | |||||||
| chrX:85073674 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG01257.hp2 HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.487-324C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073674 | |||||||
| chrX:85073744 | A | T | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.487-254A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073744 | |||||||
| chrX:85073757 | T | C | 27 | a0001c0001t0001g0097 a0001c0001t0001g0114 a0001c0001t0001g0116 others(24): Show |
27 | HG01934.hp1 HG02165.hp2 HG03942.hp1 others(24): Show |
intron_variant | MODIFIER | c.487-241T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073757 | |||||||
| chrX:85074197 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.601-77G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 7/8 | chrX | 85074197 | |||||||
| chrX:85074558 | A | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718+167A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85074558 | |||||||
| chrX:85074664 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(109): Show |
113 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.718+273A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85074664 | |||||||
| chrX:85075099 | A | G | 1 | a0001c0001t0044g0212 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.718+708A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075099 | |||||||
| chrX:85075114 | C | A | 1 | a0001c0001t0009g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.718+723C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075114 | |||||||
| chrX:85075116 | C | T | 1 | a0001c0001t0017g0120 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.718+725C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075116 | |||||||
| chrX:85075159 | T | C | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718+768T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075159 | |||||||
| chrX:85075169 | A | T | 1 | a0001c0001t0089g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+778A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075169 | |||||||
| chrX:85075487 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.718+1096T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075487 | |||||||
| chrX:85075516 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(169): Show |
174 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.718+1125A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075516 | |||||||
| chrX:85075625 | T | A | 1 | a0001c0001t0089g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1234T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075625 | |||||||
| chrX:85075652 | C | A | 1 | a0001c0001t0016g0054 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.718+1261C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075652 | |||||||
| chrX:85075903 | A | G | 1 | a0001c0001t0048g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718+1512A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075903 | |||||||
| chrX:85076014 | G | T | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.718+1623G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076014 | |||||||
| chrX:85076236 | G | T | 2 | a0001c0001t0006g0070 a0001c0001t0006g0071 |
2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.718+1845G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076236 | |||||||
| chrX:85076263 | G | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+1872G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076263 | |||||||
| chrX:85076552 | C | T | 2 | a0001c0001t0012g0121 a0001c0001t0017g0120 |
2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.718+2161C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076552 | |||||||
| chrX:85076903 | A | T | 4 | a0001c0001t0026g0161 a0001c0001t0026g0190 a0001c0001t0027g0008 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+2512A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076903 | |||||||
| chrX:85076965 | G | GT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(178): Show |
184 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.718+2583dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076965 | ||||||
| chrX:85076995 | T | TTA | 15 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(12): Show |
15 | HG00558.hp2 HG00733.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.718+2625_718+2626d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATA | 4 | a0001c0001t0032g0005 a0001c0001t0065g0083 a0001c0001t0066g0082 others(1): Show |
5 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+2623_718+2626d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(7): Show |
10 | a0001c0001t0007g0236 a0001c0001t0007g0240 a0001c0001t0007g0243 others(7): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.718+2613_718+2626d others(16): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(11): Show |
3 | a0001c0001t0007g0241 a0001c0001t0007g0245 a0001c0001t0044g0212 |
3 | HG01884.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.718+2609_718+2626d others(20): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(15): Show |
5 | a0001c0001t0004g0223 a0001c0001t0004g0230 a0001c0001t0016g0219 others(2): Show |
5 | HG01081.hp2 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+2605_718+2626d others(24): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(17): Show |
3 | a0001c0001t0004g0222 a0001c0001t0004g0224 a0001c0001t0004g0225 |
3 | HG01109.hp1 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.718+2626_718+2627i others(26): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(19): Show |
4 | a0001c0001t0004g0227 a0001c0001t0004g0229 a0001c0001t0004g0231 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+2626_718+2627i others(28): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(21): Show |
1 | a0001c0001t0004g0226 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.718+2626_718+2627i others(30): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(27): Show |
1 | a0001c0001t0010g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718+2626_718+2627i others(36): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(55): Show |
1 | a0001c0001t0014g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.718+2626_718+2627i others(64): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | T | TTATATAT others(61): Show |
2 | a0001c0001t0014g0214 a0001c0001t0014g0216 |
2 | NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.718+2626_718+2627i others(70): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | TTA | T | 30 | a0001c0001t0009g0094 a0001c0001t0009g0196 a0001c0001t0009g0197 others(27): Show |
31 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.718+2625_718+2626d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85076995 | TTATA | T | 2 | a0001c0001t0022g0009 a0001c0001t0048g0218 |
3 | HG02970.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.718+2623_718+2626d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | ||||||
| chrX:85077016 | T | C | 9 | a0001c0001t0001g0095 a0001c0001t0021g0048 a0001c0001t0021g0073 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.718+2625T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077016 | |||||||
| chrX:85077016 | T | TATATATA others(15): Show |
1 | a0001c0001t0043g0213 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.718+2626_718+2627i others(24): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077016 | ||||||
| chrX:85077044 | C | T | 3 | a0001c0001t0014g0214 a0001c0001t0014g0215 a0001c0001t0014g0216 |
3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.718+2653C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077044 | |||||||
| chrX:85077061 | G | GTA | 4 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(1): Show |
4 | HG02647.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+2683_718+2684d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077061 | ||||||
| chrX:85077061 | GTA | G | 35 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(32): Show |
35 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.718+2683_718+2684d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077061 | ||||||
| chrX:85077063 | A | G | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718+2672A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077063 | |||||||
| chrX:85077074 | T | C | 4 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 others(1): Show |
5 | HG02622.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+2683T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077074 | |||||||
| chrX:85077076 | CAT | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
135 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.718+2701_718+2702d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077076 | ||||||
| chrX:85077078 | T | C | 7 | a0001c0001t0007g0241 a0001c0001t0007g0245 a0001c0001t0025g0013 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.718+2687T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077078 | |||||||
| chrX:85077092 | T | C | 1 | a0001c0001t0011g0018 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.718+2701T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077092 | |||||||
| chrX:85077092 | T | TAC | 4 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(1): Show |
4 | HG02647.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+2709_718+2710d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077092 | ||||||
| chrX:85077102 | T | C | 2 | a0001c0001t0016g0053 a0001c0001t0033g0046 |
2 | HG01074.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.718+2711T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077102 | |||||||
| chrX:85077113 | T | A | 2 | a0001c0001t0028g0178 a0001c0001t0028g0198 |
2 | HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.718+2722T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077113 | |||||||
| chrX:85077245 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.718+2854T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077245 | |||||||
| chrX:85077264 | C | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+2873C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077264 | |||||||
| chrX:85077271 | C | T | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+2880C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077271 | |||||||
| chrX:85077353 | C | T | 1 | a0001c0001t0086g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.718+2962C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077353 | |||||||
| chrX:85077851 | G | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.718+3460G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077851 | |||||||
| chrX:85078060 | G | C | 1 | a0001c0001t0057g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.718+3669G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078060 | |||||||
| chrX:85078075 | A | C | 2 | a0001c0001t0003g0086 a0001c0001t0041g0217 |
2 | HG03486.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.718+3684A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078075 | |||||||
| chrX:85078241 | T | A | 3 | a0001c0001t0097g0066 a0001c0001t0098g0032 a0001c0001t0099g0040 |
3 | NA18955.hp1 NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.718+3850T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078241 | |||||||
| chrX:85078296 | C | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+3905C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078296 | |||||||
| chrX:85078424 | T | G | 2 | a0001c0001t0012g0117 a0001c0001t0012g0162 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.718+4033T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078424 | |||||||
| chrX:85078425 | G | C | 2 | a0001c0001t0012g0117 a0001c0001t0012g0162 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.718+4034G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078425 | |||||||
| chrX:85078443 | G | A | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718+4052G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078443 | |||||||
| chrX:85078449 | C | A | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718+4058C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078449 | |||||||
| chrX:85078498 | T | C | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0230 others(1): Show |
4 | HG01081.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+4107T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078498 | |||||||
| chrX:85078730 | C | A | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+4339C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078730 | |||||||
| chrX:85078746 | T | A | 3 | a0001c0001t0009g0197 a0001c0001t0018g0167 a0001c0001t0018g0194 |
3 | HG01243.hp1 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.718+4355T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078746 | |||||||
| chrX:85078859 | A | C | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+4468A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078859 | |||||||
| chrX:85078867 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.718+4476T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078867 | |||||||
| chrX:85078999 | A | T | 1 | a0001c0001t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.718+4608A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078999 | |||||||
| chrX:85079031 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718+4640T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079031 | |||||||
| chrX:85079230 | T | A | 1 | a0001c0001t0042g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.718+4839T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079230 | |||||||
| chrX:85079485 | G | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718+5094G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079485 | |||||||
| chrX:85079519 | G | A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0131 others(3): Show |
6 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.718+5128G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079519 | |||||||
| chrX:85079551 | C | CT | 5 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+5167dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85079551 | ||||||
| chrX:85079626 | C | T | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+5235C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079626 | |||||||
| chrX:85079845 | C | G | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.718+5454C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079845 | |||||||
| chrX:85079876 | G | A | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.718+5485G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079876 | |||||||
| chrX:85079949 | T | G | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+5558T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079949 | |||||||
| chrX:85080285 | G | A | 3 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.718+5894G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080285 | |||||||
| chrX:85080349 | C | T | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.718+5958C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080349 | |||||||
| chrX:85080497 | T | A | 1 | a0001c0001t0009g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.718+6106T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080497 | |||||||
| chrX:85080581 | G | A | 1 | a0001c0001t0077g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.718+6190G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080581 | |||||||
| chrX:85080676 | A | C | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0230 others(1): Show |
4 | HG01081.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+6285A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080676 | |||||||
| chrX:85080963 | C | G | 1 | a0001c0001t0052g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.718+6572C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080963 | |||||||
| chrX:85080976 | CTA | C | 3 | a0001c0001t0013g0007 a0001c0001t0013g0185 a0001c0001t0055g0007 |
3 | HG02922.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.718+6587_718+6588d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85080976 | ||||||
| chrX:85081065 | T | C | 1 | a0001c0001t0053g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.719-6525T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081065 | |||||||
| chrX:85081108 | G | T | 2 | a0001c0001t0071g0062 a0001c0001t0078g0033 |
2 | NA18963.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.719-6482G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081108 | |||||||
| chrX:85081228 | G | A | 2 | a0001c0001t0027g0008 a0001c0001t0058g0208 |
3 | HG01891.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.719-6362G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081228 | |||||||
| chrX:85081229 | G | A | 4 | a0001c0001t0026g0161 a0001c0001t0026g0190 a0001c0001t0027g0008 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.719-6361G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081229 | |||||||
| chrX:85081382 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(178): Show |
184 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.719-6208G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081382 | |||||||
| chrX:85081413 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.719-6177G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081413 | |||||||
| chrX:85081612 | T | C | 9 | a0001c0001t0009g0094 a0001c0001t0009g0193 a0001c0001t0009g0196 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.719-5978T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081612 | |||||||
| chrX:85081666 | T | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.719-5924T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081666 | |||||||
| chrX:85081677 | A | T | 1 | a0001c0001t0051g0221 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.719-5913A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081677 | |||||||
| chrX:85081705 | C | T | 28 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(25): Show |
28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.719-5885C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081705 | |||||||
| chrX:85081734 | C | T | 1 | a0001c0001t0053g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.719-5856C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081734 | |||||||
| chrX:85081852 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(178): Show |
184 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.719-5738G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081852 | |||||||
| chrX:85081879 | C | G | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-5711C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081879 | |||||||
| chrX:85081963 | C | T | 1 | a0001c0001t0004g0223 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.719-5627C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081963 | |||||||
| chrX:85082063 | A | G | 1 | a0001c0001t0074g0233 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.719-5527A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082063 | |||||||
| chrX:85082340 | A | G | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.719-5250A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082340 | |||||||
| chrX:85082395 | C | T | 1 | a0001c0001t0014g0216 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.719-5195C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082395 | |||||||
| chrX:85082608 | G | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(175): Show |
181 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.719-4982G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082608 | |||||||
| chrX:85082707 | A | G | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-4883A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082707 | |||||||
| chrX:85082713 | G | A | 1 | a0001c0001t0047g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.719-4877G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082713 | |||||||
| chrX:85082806 | A | C | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-4784A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082806 | |||||||
| chrX:85082921 | C | T | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-4669C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082921 | |||||||
| chrX:85083601 | T | C | 1 | a0001c0001t0035g0034 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.719-3989T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85083601 | |||||||
| chrX:85083601 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.719-3989T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85083601 | |||||||
| chrX:85083741 | T | G | 1 | a0001c0001t0050g0052 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.719-3849T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85083741 | |||||||
| chrX:85083946 | C | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.719-3644C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85083946 | |||||||
| chrX:85084109 | T | C | 1 | a0001c0001t0024g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.719-3481T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084109 | |||||||
| chrX:85084134 | C | CT | 16 | a0001c0001t0001g0097 a0001c0001t0001g0179 a0001c0001t0003g0124 others(13): Show |
17 | HG00438.hp1 HG00673.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.719-3437dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85084134 | ||||||
| chrX:85084134 | CT | C | 6 | a0001c0001t0001g0140 a0001c0001t0038g0022 a0001c0001t0039g0023 others(3): Show |
6 | HG02109.hp1 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.719-3437delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85084134 | ||||||
| chrX:85084134 | CTT | C | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.719-3438_719-3437d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85084134 | ||||||
| chrX:85084198 | C | T | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.719-3392C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084198 | |||||||
| chrX:85084380 | C | T | 2 | a0001c0001t0073g0030 a0001c0001t0083g0059 |
2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.719-3210C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084380 | |||||||
| chrX:85084404 | G | A | 4 | a0001c0001t0010g0016 a0001c0001t0010g0017 a0001c0001t0010g0024 others(1): Show |
4 | HG02647.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.719-3186G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084404 | |||||||
| chrX:85084778 | T | G | 1 | a0001c0001t0040g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.719-2812T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084778 | |||||||
| chrX:85084789 | T | G | 1 | a0001c0001t0040g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.719-2801T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084789 | |||||||
| chrX:85085087 | A | G | 1 | a0001c0001t0040g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.719-2503A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85085087 | |||||||
| chrX:85085398 | C | T | 1 | a0001c0001t0025g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.719-2192C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85085398 | |||||||
| chrX:85085399 | G | A | 1 | a0001c0001t0041g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-2191G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85085399 | |||||||
| chrX:85086042 | A | T | 2 | a0001c0001t0007g0241 a0001c0001t0007g0245 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.719-1548A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086042 | |||||||
| chrX:85086145 | A | C | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.719-1445A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086145 | |||||||
| chrX:85086192 | T | C | 2 | a0001c0001t0038g0022 a0001c0001t0039g0023 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.719-1398T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086192 | |||||||
| chrX:85086235 | C | T | 1 | a0001c0001t0093g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.719-1355C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086235 | |||||||
| chrX:85086704 | A | AT | 8 | a0001c0001t0008g0207 a0001c0001t0044g0212 a0001c0001t0061g0187 others(5): Show |
8 | HG00621.hp1 HG01884.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.719-873dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85086704 | ||||||
| chrX:85086722 | C | T | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-868C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086722 | |||||||
| chrX:85086763 | G | A | 1 | a0001c0001t0009g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.719-827G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086763 | |||||||
| chrX:85086788 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(173): Show |
179 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.719-802T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086788 | |||||||
| chrX:85086793 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(173): Show |
179 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.719-797G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086793 | |||||||
| chrX:85086800 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(173): Show |
179 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.719-790C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086800 | |||||||
| chrX:85086910 | A | G | 4 | a0001c0001t0010g0220 a0001c0001t0016g0219 a0001c0001t0048g0218 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-680A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086910 | |||||||
| chrX:85086939 | T | C | 2 | a0001c0001t0012g0117 a0001c0001t0012g0162 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.719-651T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086939 | |||||||
| chrX:85086941 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.719-649C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086941 | |||||||
| chrX:85086967 | A | G | 1 | a0001c0001t0022g0009 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.719-623A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086967 | |||||||
| chrX:85087016 | A | G | 33 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(30): Show |
33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.719-574A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087016 | |||||||
| chrX:85087022 | C | A | 1 | a0001c0001t0033g0046 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.719-568C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087022 | |||||||
| chrX:85087213 | A | G | 1 | a0001c0001t0046g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.719-377A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087213 | |||||||
| chrX:85087234 | C | T | 4 | a0001c0001t0021g0048 a0001c0001t0021g0073 a0001c0001t0021g0074 others(1): Show |
5 | HG02622.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.719-356C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087234 | |||||||
| chrX:85087297 | C | T | 1 | a0001c0001t0092g0035 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.719-293C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087297 | |||||||
| chrX:85087321 | A | G | 1 | a0001c0001t0005g0177 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.719-269A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087321 |