Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79983 |
| ensemblid | ENSG00000124429.18 |
| hgncid | 13711 |
| symbol | POF1B |
| name | POF1B actin binding protein |
| refseq_nuc | NM_024921.4 |
| refseq_prot | NP_079197.3 |
| ensembl_nuc | ENST00000262753.9 |
| ensembl_prot | ENSP00000262753.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 85277396 |
| end | 85379665 |
| strand | - |
| ver | v1.2 |
| region | chrX:85277396-85379665 |
| region5000 | chrX:85272396-85384665 |
| regionname0 | POF1B_chrX_85277396_85379665 |
| regionname5000 | POF1B_chrX_85272396_85384665 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 589 | 198 | 53 | 25 | 89 | 6 | 24 | 70 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| a0002 | 1/0 | 589 | 13 | 5 | 5 | 1 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| a0003 | 0/0 | 589 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| a0004 | 0/0 | 589 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| a0005 | 0/0 | 589 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| a0006 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| a0007 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| a0008 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| a0009 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | MSSSY others(584): Show |
chrX | 85272396 | 85384665 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1767 | 154 | 25 | 19 | 81 | 6 | 22 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0001c0002 | 0/0 | 1767 | 33 | 21 | 3 | 7 | 0 | 2 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0001c0004 | 0/0 | 1767 | 9 | 6 | 3 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0001c0008 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0001c0009 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0002c0003 | 1/0 | 1767 | 13 | 5 | 5 | 1 | 1 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0003c0005 | 0/0 | 1767 | 7 | 6 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0004c0007 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0004c0013 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0005c0006 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0006c0011 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0007c0012 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0008c0014 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 | ||
| a0009c0010 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | ATGAG others(1762): Show |
chrX | 85272396 | 85384665 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3863 | 71 | 11 | 11 | 30 | 3 | 16 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0001t0002 | 0/0 | 3863 | 53 | 6 | 6 | 40 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0001t0003 | 0/1 | 3863 | 23 | 5 | 2 | 8 | 3 | 4 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0001t0009 | 0/0 | 3864 | 2 | 1 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3859): Show |
chrX | 85272396 | 85384665 |
| a0001c0001t0011 | 0/0 | 3863 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0001t0012 | 0/0 | 3863 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0001t0013 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0001t0016 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3859): Show |
chrX | 85272396 | 85384665 |
| a0001c0001t0017 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3859): Show |
chrX | 85272396 | 85384665 |
| a0001c0002t0004 | 0/0 | 3863 | 25 | 15 | 2 | 6 | 0 | 2 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0002t0006 | 0/0 | 3863 | 2 | 2 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0002t0007 | 0/0 | 3863 | 2 | 2 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0002t0008 | 0/0 | 3864 | 2 | 0 | 1 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3859): Show |
chrX | 85272396 | 85384665 |
| a0001c0002t0010 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0002t0015 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0004t0003 | 0/0 | 3863 | 9 | 6 | 3 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0008t0014 | 0/0 | 3863 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0001c0009t0002 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0002c0003t0001 | 0/0 | 3863 | 7 | 0 | 5 | 1 | 1 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0002c0003t0005 | 0/0 | 3863 | 5 | 5 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0002c0003t0018 | 1/0 | 3863 | 1 | 0 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0003c0005t0001 | 0/0 | 3863 | 7 | 6 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0004c0007t0001 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0004c0007t0003 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0004c0013t0003 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0005c0006t0004 | 0/0 | 3863 | 2 | 2 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0006c0011t0001 | 0/0 | 3863 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0007c0012t0001 | 0/0 | 3863 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0008c0014t0004 | 0/0 | 3863 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| a0009c0010t0002 | 0/0 | 3863 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | GCCAG others(3858): Show |
chrX | 85272396 | 85384665 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0012g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0016g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0001t0017g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0002t0015g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0004t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0004t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0004t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0004t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0004t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0004t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0004t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0008t0014g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0001c0009t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0002c0003t0018g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0003c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0003c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0003c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0003c0005t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0003c0005t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0003c0005t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0003c0005t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0004c0007t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0004c0007t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0004c0013t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0005c0006t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0005c0006t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0006c0011t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0007c0012t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0008c0014t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| a0009c0010t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0052 | EUR | GBR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0053 | EUR | FIN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0092 | EAS | CHS | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00673 | hp1 | a0001 | c0002 | t0004 | g0190 | EAS | CHS | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0026 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG00738 | hp1 | a0001 | c0004 | t0003 | g0203 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0093 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0107 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0100 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01167 | hp1 | a0001 | c0004 | t0003 | g0201 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01169 | hp2 | a0001 | c0004 | t0003 | g0202 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0021 | AMR | PUR | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01255 | hp1 | a0003 | c0005 | t0001 | g0181 | AMR | CLM | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0097 | AMR | CLM | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0104 | AMR | CLM | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0171 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01891 | hp2 | a0001 | c0002 | t0010 | g0035 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PEL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01981 | hp1 | a0001 | c0002 | t0008 | g0192 | AMR | PEL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02055 | hp1 | a0004 | c0007 | t0003 | g0038 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02071 | hp1 | a0006 | c0011 | t0001 | g0022 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02257 | hp2 | a0004 | c0007 | t0001 | g0039 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02280 | hp2 | a0003 | c0005 | t0001 | g0178 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02451 | hp2 | a0003 | c0005 | t0001 | g0180 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02615 | hp1 | a0005 | c0006 | t0004 | g0031 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02615 | hp2 | a0003 | c0005 | t0001 | g0165 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0028 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0209 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0167 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02647 | hp1 | a0001 | c0009 | t0002 | g0144 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02717 | hp1 | a0004 | c0013 | t0003 | g0040 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02723 | hp2 | a0001 | c0002 | t0004 | g0173 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02809 | hp1 | a0001 | c0004 | t0003 | g0200 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0019 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02895 | hp1 | a0001 | c0004 | t0003 | g0198 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02897 | hp2 | a0001 | c0004 | t0003 | g0199 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02922 | hp1 | a0002 | c0003 | t0005 | g0101 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02965 | hp1 | a0003 | c0005 | t0001 | g0164 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0142 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02970 | hp2 | a0001 | c0002 | t0007 | g0176 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0045 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03041 | hp1 | a0007 | c0012 | t0001 | g0037 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0113 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03139 | hp1 | a0002 | c0003 | t0005 | g0098 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03195 | hp1 | a0002 | c0003 | t0005 | g0006 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03225 | hp1 | a0001 | c0004 | t0003 | g0015 | AFR | MSL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03453 | hp1 | a0005 | c0006 | t0004 | g0030 | AFR | MSL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0169 | AFR | MSL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03516 | hp1 | a0001 | c0002 | t0007 | g0175 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03516 | hp2 | a0002 | c0003 | t0005 | g0006 | AFR | ESN | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0172 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03540 | hp2 | a0002 | c0003 | t0005 | g0088 | AFR | GWD | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03831 | hp1 | a0001 | c0002 | t0004 | g0195 | SAS | BEB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0076 | SAS | BEB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | BEB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | STU | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18522 | hp1 | a0003 | c0005 | t0001 | g0179 | AFR | YRI | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | YRI | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18906 | hp2 | a0001 | c0004 | t0003 | g0036 | AFR | YRI | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18939 | hp1 | a0008 | c0014 | t0004 | g0205 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0196 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18951 | hp2 | a0001 | c0002 | t0004 | g0016 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18981 | hp1 | a0001 | c0008 | t0014 | g0018 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18984 | hp1 | a0001 | c0001 | t0012 | g0123 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18985 | hp2 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18989 | hp1 | a0001 | c0001 | t0017 | g0134 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18993 | hp1 | a0001 | c0002 | t0008 | g0191 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0016 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19010 | hp1 | a0001 | c0002 | t0004 | g0166 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19011 | hp2 | a0001 | c0002 | t0004 | g0194 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19030 | hp1 | a0001 | c0002 | t0015 | g0029 | AFR | LWK | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0137 | AFR | LWK | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0182 | AFR | LWK | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19066 | hp1 | a0009 | c0010 | t0002 | g0116 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0099 | EUR | TSI | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0010 | EUR | TSI | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA20905 | hp1 | a0001 | c0002 | t0004 | g0193 | SAS | GIH | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02109 | hp1 | a0001 | c0002 | t0006 | g0159 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02109 | hp2 | a0003 | c0005 | t0001 | g0168 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0141 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0174 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG02559 | hp2 | a0001 | c0002 | t0006 | g0160 | AFR | ACB | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG06807 | hp1 | a0001 | c0004 | t0003 | g0015 | AFR | USA | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0027 | AFR | USA | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0118 | REF | REF | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0018 | g0102 | REF | REF | POF1B_chrX_85272396_85384665 | POF1B | chrX | 85272396 | 85384665 |
| 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:85308129 | T | A | 8 | a0001 a0003 a0004 others(5): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
missense_variant | MODERATE | c.1045A>T | p.Met349Leu | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 10/17 | 1113/3863 | 1045/1770 | 349/589 | chrX | 85308129 | |||
| chrX:85330997 | G | A | 1 | a0009 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.806C>T | p.Thr269Met | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/17 | 874/3863 | 806/1770 | 269/589 | chrX | 85330997 | |||
| chrX:85345942 | T | C | 1 | a0003 | 7 | HG01255.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
missense_variant | MODERATE | c.641A>G | p.Gln214Arg | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/17 | 709/3863 | 641/1770 | 214/589 | chrX | 85345942 | |||
| chrX:85345964 | G | A | 1 | a0005 | 2 | HG02615.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.619C>T | p.Pro207Ser | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/17 | 687/3863 | 619/1770 | 207/589 | chrX | 85345964 | |||
| chrX:85367724 | T | G | 1 | a0006 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.325A>C | p.Ser109Arg | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/17 | 393/3863 | 325/1770 | 109/589 | chrX | 85367724 | |||
| chrX:85379264 | T | C | 1 | a0007 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.191A>G | p.Gln64Arg | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/17 | 259/3863 | 191/1770 | 64/589 | chrX | 85379264 | |||
| chrX:85379342 | T | G | 1 | a0004 | 3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.113A>C | p.Gln38Pro | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/17 | 181/3863 | 113/1770 | 38/589 | chrX | 85379342 | |||
| chrX:85379436 | T | C | 1 | a0008 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.19A>G | p.Ser7Gly | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/17 | 87/3863 | 19/1770 | 7/589 | chrX | 85379436 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:85303483 | G | C | 3 | a0001c0002 a0005c0006 a0008c0014 |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
synonymous_variant | LOW | c.1572C>G | p.Leu524Leu | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/17 | 1640/3863 | 1572/1770 | 524/589 | chrX | 85303483 | |||
| chrX:85305854 | G | A | 2 | a0001c0004 a0004c0013 |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
synonymous_variant | LOW | c.1374C>T | p.Asn458Asn | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/17 | 1442/3863 | 1374/1770 | 458/589 | chrX | 85305854 | |||
| chrX:85305857 | G | C | 1 | a0001c0009 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1371C>G | p.Gly457Gly | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/17 | 1439/3863 | 1371/1770 | 457/589 | chrX | 85305857 | |||
| chrX:85379371 | C | T | 1 | a0001c0008 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.84G>A | p.Gln28Gln | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/17 | 152/3863 | 84/1770 | 28/589 | chrX | 85379371 |
| 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:85277572 | C | T | 8 | a0001c0001t0013 a0001c0002t0004 a0001c0002t0007 others(5): Show |
35 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1849G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 1849 | chrX | 85277572 | ||||||
| chrX:85277655 | G | A | 1 | a0001c0001t0013 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1766C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 1766 | chrX | 85277655 | ||||||
| chrX:85277795 | C | T | 16 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(13): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1626G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 1626 | chrX | 85277795 | ||||||
| chrX:85277990 | T | G | 16 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(13): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1431A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 1431 | chrX | 85277990 | ||||||
| chrX:85278248 | G | T | 1 | a0002c0003t0005 | 5 | HG02922.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1173C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 1173 | chrX | 85278248 | ||||||
| chrX:85278402 | G | T | 16 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(13): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1019C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 1019 | chrX | 85278402 | ||||||
| chrX:85278442 | T | C | 1 | a0001c0008t0014 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 979 | chrX | 85278442 | ||||||
| chrX:85278571 | A | G | 1 | a0001c0001t0012 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 850 | chrX | 85278571 | ||||||
| chrX:85278752 | A | G | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0017 others(4): Show |
37 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*669T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 669 | chrX | 85278752 | ||||||
| chrX:85278880 | G | A | 1 | a0001c0001t0011 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 541 | chrX | 85278880 | ||||||
| chrX:85279038 | A | G | 1 | a0001c0002t0010 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 383 | chrX | 85279038 | ||||||
| chrX:85279053 | C | A | 4 | a0001c0001t0002 a0001c0001t0016 a0001c0009t0002 others(1): Show |
56 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*368G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 368 | chrX | 85279053 | ||||||
| chrX:85279108 | G | A | 1 | a0001c0002t0007 | 2 | HG02970.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*313C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 313 | chrX | 85279108 | ||||||
| chrX:85279109 | T | G | 16 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(13): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*312A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 312 | chrX | 85279109 | ||||||
| chrX:85279153 | A | C | 8 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0007 others(5): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*268T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 268 | chrX | 85279153 | ||||||
| chrX:85279228 | G | C | 1 | a0001c0002t0015 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 193 | chrX | 85279228 | ||||||
| chrX:85279376 | A | AC | 4 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0017 others(1): Show |
6 | HG01981.hp1 HG03453.hp2 NA18985.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*44_*45insG | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 44 | chrX | 85279376 | ||||||
| chrX:85279377 | A | C | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*44T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 17/17 | 44 | chrX | 85279377 |
| 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:85279476 | CATT | C | 33 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(30): Show |
34 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1765-53_1765-51del others(3): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85279476 | |||||||
| chrX:85279613 | T | C | 35 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(32): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1765-187A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85279613 | |||||||
| chrX:85279780 | A | T | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1765-354T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85279780 | |||||||
| chrX:85279801 | A | G | 10 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0190 others(7): Show |
11 | HG00673.hp1 HG01981.hp1 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.1765-375T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85279801 | |||||||
| chrX:85279983 | C | A | 7 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(4): Show |
7 | HG00735.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1765-557G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85279983 | |||||||
| chrX:85280022 | CTAAT | C | 2 | a0001c0002t0004g0138 a0001c0002t0004g0141 |
2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1765-600_1765-597d others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280022 | |||||||
| chrX:85280167 | T | G | 126 | a0001c0001t0001g0177 a0001c0001t0002g0002 a0001c0001t0002g0003 others(123): Show |
138 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1765-741A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280167 | |||||||
| chrX:85280211 | G | A | 9 | a0001c0001t0001g0177 a0003c0005t0001g0164 a0003c0005t0001g0165 others(6): Show |
9 | HG01255.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1765-785C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280211 | |||||||
| chrX:85280445 | A | G | 35 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(32): Show |
38 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1765-1019T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280445 | |||||||
| chrX:85280560 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1765-1134A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280560 | |||||||
| chrX:85280872 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1764+1331T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280872 | |||||||
| chrX:85280884 | C | T | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1764+1319G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280884 | |||||||
| chrX:85280934 | G | A | 1 | a0001c0002t0004g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1764+1269C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280934 | |||||||
| chrX:85280949 | G | A | 1 | a0001c0002t0004g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1764+1254C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280949 | |||||||
| chrX:85280962 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1764+1241G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85280962 | |||||||
| chrX:85281069 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1764+1134G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281069 | |||||||
| chrX:85281179 | CT | C | 59 | a0001c0001t0001g0139 a0001c0001t0003g0010 a0001c0001t0003g0011 others(56): Show |
63 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1764+1023delA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281179 | |||||||
| chrX:85281179 | CTT | C | 6 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0142 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1764+1022_1764+102 others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281179 | |||||||
| chrX:85281334 | T | G | 1 | a0001c0002t0004g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1764+869A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281334 | |||||||
| chrX:85281730 | A | AAT | 38 | a0001c0001t0001g0050 a0001c0001t0001g0071 a0001c0001t0013g0167 others(35): Show |
39 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1764+471_1764+472d others(4): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281730 | |||||||
| chrX:85281863 | G | GC | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1764+339_1764+340i others(3): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281863 | |||||||
| chrX:85281868 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1764+335T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281868 | |||||||
| chrX:85281872 | A | G | 15 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0171 others(12): Show |
16 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1764+331T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281872 | |||||||
| chrX:85281915 | C | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0185 a0001c0001t0009g0169 |
3 | HG02258.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1764+288G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85281915 | |||||||
| chrX:85282065 | G | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1764+138C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85282065 | |||||||
| chrX:85282126 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1764+77A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85282126 | |||||||
| chrX:85282167 | G | A | 2 | a0001c0001t0003g0184 a0004c0007t0003g0038 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1764+36C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85282167 | |||||||
| chrX:85282200 | T | C | 1 | a0006c0011t0001g0022 | 1 | HG02071.hp1 | splice_region_variant&intron_variant | LOW | c.1764+3A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 16/16 | chrX | 85282200 | |||||||
| chrX:85282394 | G | T | 1 | a0001c0002t0004g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1650-77C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85282394 | |||||||
| chrX:85282633 | G | C | 1 | a0001c0001t0003g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1650-316C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85282633 | |||||||
| chrX:85282738 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-421T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85282738 | |||||||
| chrX:85282780 | T | TA | 36 | a0001c0001t0013g0167 a0001c0002t0004g0016 a0001c0002t0004g0019 others(33): Show |
37 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1650-464dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85282780 | |||||||
| chrX:85282831 | A | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-514T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85282831 | |||||||
| chrX:85283154 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1650-837C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283154 | |||||||
| chrX:85283232 | C | T | 1 | a0001c0001t0003g0083 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1650-915G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283232 | |||||||
| chrX:85283330 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-1013A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283330 | |||||||
| chrX:85283480 | C | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1650-1163G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283480 | |||||||
| chrX:85283569 | A | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
6 | HG01261.hp1 NA18951.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1650-1252T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283569 | |||||||
| chrX:85283586 | C | T | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-1269G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283586 | |||||||
| chrX:85283682 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0151 |
2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1650-1365G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283682 | |||||||
| chrX:85283703 | G | C | 1 | a0001c0001t0002g0143 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1650-1386C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283703 | |||||||
| chrX:85283708 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1650-1391G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85283708 | |||||||
| chrX:85284073 | A | T | 1 | a0001c0001t0002g0023 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1650-1756T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284073 | |||||||
| chrX:85284593 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0082 others(1): Show |
4 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1650-2276C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284593 | |||||||
| chrX:85284644 | CA | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-2328delT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284644 | |||||||
| chrX:85284650 | T | C | 1 | a0001c0002t0004g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1650-2333A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284650 | |||||||
| chrX:85284666 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650-2349A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284666 | |||||||
| chrX:85284676 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650-2359T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284676 | |||||||
| chrX:85284676 | A | T | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-2359T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284676 | |||||||
| chrX:85284677 | A | G | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-2360T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284677 | |||||||
| chrX:85284726 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650-2409G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284726 | |||||||
| chrX:85284742 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650-2425C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284742 | |||||||
| chrX:85284745 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650-2428C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284745 | |||||||
| chrX:85284750 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650-2433T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284750 | |||||||
| chrX:85284760 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650-2443T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85284760 | |||||||
| chrX:85285128 | G | A | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-2811C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285128 | |||||||
| chrX:85285190 | T | C | 13 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0171 others(10): Show |
14 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1650-2873A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285190 | |||||||
| chrX:85285239 | G | C | 2 | a0001c0002t0004g0045 a0001c0002t0004g0113 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1650-2922C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285239 | |||||||
| chrX:85285313 | C | T | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1650-2996G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285313 | |||||||
| chrX:85285414 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-3097T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285414 | |||||||
| chrX:85285725 | C | T | 15 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0171 others(12): Show |
16 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1650-3408G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285725 | |||||||
| chrX:85285811 | T | A | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1650-3494A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285811 | |||||||
| chrX:85285890 | C | T | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1650-3573G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285890 | |||||||
| chrX:85285918 | G | GAGA | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-3604_1650-360 others(7): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285918 | |||||||
| chrX:85285933 | A | G | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-3616T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285933 | |||||||
| chrX:85285937 | G | T | 1 | a0002c0003t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1650-3620C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85285937 | |||||||
| chrX:85286146 | T | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-3829A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286146 | |||||||
| chrX:85286180 | A | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1650-3863T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286180 | |||||||
| chrX:85286255 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1650-3938C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286255 | |||||||
| chrX:85286447 | A | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-4130T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286447 | |||||||
| chrX:85286525 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1650-4208T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286525 | |||||||
| chrX:85286609 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1650-4292A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286609 | |||||||
| chrX:85286700 | T | A | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1650-4383A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286700 | |||||||
| chrX:85286840 | T | C | 9 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1650-4523A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286840 | |||||||
| chrX:85286985 | T | C | 1 | a0001c0001t0002g0014 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1650-4668A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85286985 | |||||||
| chrX:85287041 | T | A | 3 | a0001c0002t0004g0028 a0001c0002t0006g0159 a0001c0002t0006g0160 |
3 | HG02109.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1650-4724A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85287041 | |||||||
| chrX:85287057 | A | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0185 a0001c0001t0009g0169 |
3 | HG02258.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1650-4740T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85287057 | |||||||
| chrX:85287283 | T | C | 1 | a0001c0002t0015g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1650-4966A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85287283 | |||||||
| chrX:85287337 | C | A | 10 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-5020G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85287337 | |||||||
| chrX:85287682 | A | G | 32 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(29): Show |
35 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1650-5365T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85287682 | |||||||
| chrX:85287833 | G | C | 1 | a0001c0001t0002g0008 | 2 | NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1650-5516C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85287833 | |||||||
| chrX:85288013 | T | G | 1 | a0001c0001t0002g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1650-5696A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288013 | |||||||
| chrX:85288017 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1650-5700C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288017 | |||||||
| chrX:85288139 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-5822T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288139 | |||||||
| chrX:85288282 | G | A | 1 | a0004c0007t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1650-5965C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288282 | |||||||
| chrX:85288288 | T | C | 1 | a0001c0001t0002g0007 | 2 | NA18953.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1650-5971A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288288 | |||||||
| chrX:85288698 | C | G | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1650-6381G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288698 | |||||||
| chrX:85288760 | C | A | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-6443G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288760 | |||||||
| chrX:85288764 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-6447A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288764 | |||||||
| chrX:85288768 | A | C | 1 | a0001c0001t0001g0057 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1650-6451T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288768 | |||||||
| chrX:85288827 | A | G | 23 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(20): Show |
25 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1650-6510T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85288827 | |||||||
| chrX:85289185 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1650-6868C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289185 | |||||||
| chrX:85289270 | G | A | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-6953C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289270 | |||||||
| chrX:85289396 | T | G | 36 | a0001c0001t0013g0167 a0001c0002t0004g0016 a0001c0002t0004g0019 others(33): Show |
37 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1650-7079A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289396 | |||||||
| chrX:85289451 | A | C | 1 | a0002c0003t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1650-7134T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289451 | |||||||
| chrX:85289548 | A | T | 23 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(20): Show |
25 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1650-7231T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289548 | |||||||
| chrX:85289697 | G | A | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-7380C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289697 | |||||||
| chrX:85289745 | T | C | 9 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1650-7428A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289745 | |||||||
| chrX:85289798 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0070 |
2 | HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1650-7481C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289798 | |||||||
| chrX:85289810 | G | A | 1 | a0002c0003t0001g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1650-7493C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85289810 | |||||||
| chrX:85290044 | T | C | 1 | a0001c0002t0004g0016 | 2 | NA18951.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1650-7727A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290044 | |||||||
| chrX:85290185 | C | T | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-7868G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290185 | |||||||
| chrX:85290287 | AT | A | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1650-7971delA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290287 | |||||||
| chrX:85290289 | T | G | 1 | a0001c0001t0003g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1650-7972A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290289 | |||||||
| chrX:85290298 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-7981T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290298 | |||||||
| chrX:85290367 | G | A | 32 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(29): Show |
35 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1650-8050C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290367 | |||||||
| chrX:85290403 | C | T | 1 | a0001c0001t0002g0008 | 2 | NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1650-8086G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290403 | |||||||
| chrX:85290410 | A | G | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1650-8093T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290410 | |||||||
| chrX:85290438 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1650-8121C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290438 | |||||||
| chrX:85290499 | A | C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-8182T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290499 | |||||||
| chrX:85290715 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1650-8398G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290715 | |||||||
| chrX:85290973 | C | T | 10 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0190 others(7): Show |
11 | HG00673.hp1 HG01981.hp1 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.1650-8656G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290973 | |||||||
| chrX:85290974 | G | A | 1 | a0001c0002t0004g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1650-8657C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85290974 | |||||||
| chrX:85291075 | A | G | 1 | a0001c0001t0001g0025 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1650-8758T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85291075 | |||||||
| chrX:85291273 | A | G | 13 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0171 others(10): Show |
14 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1650-8956T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85291273 | |||||||
| chrX:85291719 | GCTTGA | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0070 |
2 | HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1650-9407_1650-940 others(9): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85291719 | |||||||
| chrX:85291953 | A | G | 1 | a0001c0002t0015g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1650-9636T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85291953 | |||||||
| chrX:85291999 | T | A | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1650-9682A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85291999 | |||||||
| chrX:85292030 | G | T | 10 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-9713C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292030 | |||||||
| chrX:85292147 | G | A | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-9830C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292147 | |||||||
| chrX:85292265 | C | G | 1 | a0001c0002t0004g0026 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1650-9948G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292265 | |||||||
| chrX:85292270 | A | T | 1 | a0001c0001t0003g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1650-9953T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292270 | |||||||
| chrX:85292359 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1650-10042C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292359 | |||||||
| chrX:85292367 | G | A | 1 | a0001c0001t0012g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1650-10050C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292367 | |||||||
| chrX:85292388 | G | T | 1 | a0001c0002t0015g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1650-10071C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292388 | |||||||
| chrX:85292783 | A | G | 1 | a0001c0002t0004g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1650-10466T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292783 | |||||||
| chrX:85292846 | T | TA | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1650-10530dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85292846 | |||||||
| chrX:85293007 | C | T | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+10399G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293007 | |||||||
| chrX:85293282 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1649+10124T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293282 | |||||||
| chrX:85293503 | C | T | 3 | a0001c0002t0004g0171 a0001c0002t0004g0173 a0001c0002t0004g0174 |
3 | HG01891.hp1 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1649+9903G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293503 | |||||||
| chrX:85293607 | C | G | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1649+9799G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293607 | |||||||
| chrX:85293668 | T | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1649+9738A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293668 | |||||||
| chrX:85293778 | G | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1649+9628C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293778 | |||||||
| chrX:85293847 | G | A | 10 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649+9559C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293847 | |||||||
| chrX:85293929 | A | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+9477T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293929 | |||||||
| chrX:85293971 | CA | C | 32 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(29): Show |
35 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1649+9434delT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293971 | |||||||
| chrX:85293980 | A | AT | 35 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(32): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1649+9425_1649+942 others(5): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85293980 | |||||||
| chrX:85294035 | G | T | 26 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(23): Show |
27 | HG00673.hp1 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1649+9371C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85294035 | |||||||
| chrX:85294074 | G | A | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1649+9332C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85294074 | |||||||
| chrX:85294238 | G | A | 4 | a0001c0001t0001g0155 a0001c0001t0001g0170 a0001c0001t0001g0185 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+9168C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85294238 | |||||||
| chrX:85294290 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1649+9116C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85294290 | |||||||
| chrX:85294565 | C | T | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+8841G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85294565 | |||||||
| chrX:85294870 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1649+8536T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85294870 | |||||||
| chrX:85294980 | C | T | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649+8426G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85294980 | |||||||
| chrX:85295042 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1649+8364C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85295042 | |||||||
| chrX:85295357 | G | C | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1649+8049C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85295357 | |||||||
| chrX:85295762 | C | T | 1 | a0003c0005t0001g0164 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1649+7644G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85295762 | |||||||
| chrX:85295870 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1649+7536G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85295870 | |||||||
| chrX:85296051 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0185 a0001c0001t0009g0169 |
3 | HG02258.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1649+7355C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296051 | |||||||
| chrX:85296101 | A | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+7305T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296101 | |||||||
| chrX:85296254 | C | T | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1649+7152G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296254 | |||||||
| chrX:85296259 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0185 a0001c0001t0009g0169 |
3 | HG02258.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1649+7147G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296259 | |||||||
| chrX:85296315 | G | A | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649+7091C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296315 | |||||||
| chrX:85296425 | A | G | 1 | a0002c0003t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1649+6981T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296425 | |||||||
| chrX:85296668 | C | T | 1 | a0001c0009t0002g0144 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1649+6738G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296668 | |||||||
| chrX:85296700 | C | T | 1 | a0001c0004t0003g0015 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1649+6706G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296700 | |||||||
| chrX:85296934 | AT | A | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1649+6471delA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85296934 | |||||||
| chrX:85297036 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1649+6370A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85297036 | |||||||
| chrX:85297079 | C | T | 2 | a0001c0002t0004g0045 a0001c0002t0004g0113 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1649+6327G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85297079 | |||||||
| chrX:85297345 | C | T | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1649+6061G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85297345 | |||||||
| chrX:85297510 | T | C | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1649+5896A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85297510 | |||||||
| chrX:85297675 | T | TG | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1649+5730dupC | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85297675 | |||||||
| chrX:85297897 | C | T | 1 | a0001c0002t0004g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1649+5509G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85297897 | |||||||
| chrX:85298145 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1649+5261C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85298145 | |||||||
| chrX:85298419 | A | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+4987T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85298419 | |||||||
| chrX:85298687 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1649+4719C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85298687 | |||||||
| chrX:85298819 | A | G | 17 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0052 others(14): Show |
19 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1649+4587T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85298819 | |||||||
| chrX:85299134 | A | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+4272T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299134 | |||||||
| chrX:85299191 | CT | C | 34 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0057 others(31): Show |
35 | HG00673.hp1 HG00735.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1649+4214delA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299191 | |||||||
| chrX:85299191 | CTT | C | 46 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(43): Show |
49 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1649+4213_1649+421 others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299191 | |||||||
| chrX:85299215 | G | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+4191C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299215 | |||||||
| chrX:85299302 | T | A | 41 | a0001c0001t0003g0011 a0001c0001t0003g0056 a0001c0001t0003g0135 others(38): Show |
43 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.1649+4104A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299302 | |||||||
| chrX:85299302 | T | TA | 18 | a0001c0001t0003g0010 a0001c0001t0003g0043 a0001c0001t0003g0052 others(15): Show |
19 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1649+4103_1649+410 others(5): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299302 | |||||||
| chrX:85299302 | T | TTA | 10 | a0001c0001t0013g0167 a0001c0004t0003g0015 a0001c0004t0003g0036 others(7): Show |
11 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1649+4103_1649+410 others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299302 | |||||||
| chrX:85299327 | C | T | 1 | a0002c0003t0001g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1649+4079G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299327 | |||||||
| chrX:85299446 | G | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0007 others(38): Show |
48 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1649+3960C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299446 | |||||||
| chrX:85299449 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+3957A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299449 | |||||||
| chrX:85299479 | C | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+3927G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299479 | |||||||
| chrX:85299548 | A | G | 1 | a0003c0005t0001g0179 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1649+3858T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299548 | |||||||
| chrX:85299617 | A | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+3789T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299617 | |||||||
| chrX:85299653 | C | T | 10 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649+3753G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299653 | |||||||
| chrX:85299667 | G | C | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1649+3739C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299667 | |||||||
| chrX:85299670 | A | AT | 12 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0028 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1649+3735_1649+373 others(5): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299670 | |||||||
| chrX:85299671 | A | T | 35 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(32): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1649+3735T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299671 | |||||||
| chrX:85299699 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0027 |
2 | HG00735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1649+3707C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299699 | |||||||
| chrX:85299800 | G | A | 1 | a0004c0013t0003g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1649+3606C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299800 | |||||||
| chrX:85299865 | G | A | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1649+3541C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85299865 | |||||||
| chrX:85300337 | C | T | 1 | a0001c0009t0002g0144 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1649+3069G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85300337 | |||||||
| chrX:85300456 | G | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1649+2950C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85300456 | |||||||
| chrX:85300766 | G | A | 9 | a0001c0001t0001g0177 a0003c0005t0001g0164 a0003c0005t0001g0165 others(6): Show |
9 | HG01255.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1649+2640C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85300766 | |||||||
| chrX:85300915 | C | G | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1649+2491G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85300915 | |||||||
| chrX:85300916 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1649+2490G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85300916 | |||||||
| chrX:85300988 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1649+2418G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85300988 | |||||||
| chrX:85301141 | C | T | 33 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1649+2265G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85301141 | |||||||
| chrX:85301215 | A | T | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1649+2191T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85301215 | |||||||
| chrX:85301236 | A | G | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1649+2170T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85301236 | |||||||
| chrX:85301251 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1649+2155C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85301251 | |||||||
| chrX:85301300 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1649+2106T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85301300 | |||||||
| chrX:85301425 | A | C | 1 | a0001c0004t0003g0015 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1649+1981T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85301425 | |||||||
| chrX:85301701 | T | G | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1649+1705A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85301701 | |||||||
| chrX:85302161 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1649+1245T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302161 | |||||||
| chrX:85302222 | A | G | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0045 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1649+1184T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302222 | |||||||
| chrX:85302223 | T | C | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1649+1183A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302223 | |||||||
| chrX:85302425 | G | A | 1 | a0003c0005t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1649+981C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302425 | |||||||
| chrX:85302441 | A | C | 1 | a0001c0002t0015g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1649+965T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302441 | |||||||
| chrX:85302562 | C | G | 2 | a0001c0002t0004g0045 a0001c0002t0004g0113 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1649+844G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302562 | |||||||
| chrX:85302628 | C | T | 9 | a0001c0001t0001g0177 a0003c0005t0001g0164 a0003c0005t0001g0165 others(6): Show |
9 | HG01255.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1649+778G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302628 | |||||||
| chrX:85302687 | G | A | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1649+719C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302687 | |||||||
| chrX:85302723 | G | C | 17 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0052 others(14): Show |
19 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1649+683C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302723 | |||||||
| chrX:85302755 | C | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1649+651G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302755 | |||||||
| chrX:85302803 | T | C | 1 | a0001c0001t0003g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1649+603A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85302803 | |||||||
| chrX:85303054 | A | G | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1649+352T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85303054 | |||||||
| chrX:85303075 | A | G | 1 | a0001c0002t0004g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1649+331T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85303075 | |||||||
| chrX:85303234 | T | G | 3 | a0003c0005t0001g0179 a0003c0005t0001g0180 a0003c0005t0001g0181 |
3 | HG01255.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1649+172A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85303234 | |||||||
| chrX:85303239 | T | TGACCACA others(3): Show |
1 | a0001c0001t0001g0060 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1649+157_1649+166d others(12): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85303239 | |||||||
| chrX:85303267 | A | C | 35 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(32): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1649+139T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 15/16 | chrX | 85303267 | |||||||
| chrX:85303502 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1567-14C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 14/16 | chrX | 85303502 | |||||||
| chrX:85303902 | C | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1567-414G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 14/16 | chrX | 85303902 | |||||||
| chrX:85304012 | TATAA | T | 4 | a0002c0003t0005g0006 a0002c0003t0005g0088 a0002c0003t0005g0098 others(1): Show |
5 | HG02922.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1566+327_1566+330d others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 14/16 | chrX | 85304012 | |||||||
| chrX:85304171 | G | T | 78 | a0001c0001t0001g0177 a0001c0001t0003g0010 a0001c0001t0003g0011 others(75): Show |
82 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.1566+172C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 14/16 | chrX | 85304171 | |||||||
| chrX:85304295 | G | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1566+48C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 14/16 | chrX | 85304295 | |||||||
| chrX:85304304 | T | C | 9 | a0001c0001t0001g0177 a0003c0005t0001g0164 a0003c0005t0001g0165 others(6): Show |
9 | HG01255.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1566+39A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 14/16 | chrX | 85304304 | |||||||
| chrX:85304333 | C | T | 2 | a0001c0002t0004g0026 a0001c0002t0004g0027 |
2 | HG00735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1566+10G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 14/16 | chrX | 85304333 | |||||||
| chrX:85304556 | A | G | 1 | a0006c0011t0001g0022 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1438-85T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/16 | chrX | 85304556 | |||||||
| chrX:85304557 | A | T | 1 | a0001c0001t0003g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1438-86T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/16 | chrX | 85304557 | |||||||
| chrX:85304607 | G | T | 23 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(20): Show |
25 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1438-136C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/16 | chrX | 85304607 | |||||||
| chrX:85305357 | C | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1437+434G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/16 | chrX | 85305357 | |||||||
| chrX:85305370 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1437+421G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/16 | chrX | 85305370 | |||||||
| chrX:85305541 | A | C | 10 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1437+250T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/16 | chrX | 85305541 | |||||||
| chrX:85305645 | G | A | 1 | a0001c0002t0015g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1437+146C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/16 | chrX | 85305645 | |||||||
| chrX:85305708 | G | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0133 a0001c0001t0002g0187 others(1): Show |
6 | NA18944.hp1 NA18986.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1437+83C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 13/16 | chrX | 85305708 | |||||||
| chrX:85306363 | A | G | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1165-30T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 11/16 | chrX | 85306363 | |||||||
| chrX:85306459 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 |
3 | HG02572.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1165-126C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 11/16 | chrX | 85306459 | |||||||
| chrX:85306459 | G | C | 68 | a0001c0001t0002g0114 a0001c0001t0003g0010 a0001c0001t0003g0011 others(65): Show |
72 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.1165-126C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 11/16 | chrX | 85306459 | |||||||
| chrX:85306522 | A | G | 70 | a0001c0001t0002g0114 a0001c0001t0003g0010 a0001c0001t0003g0011 others(67): Show |
74 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.1165-189T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 11/16 | chrX | 85306522 | |||||||
| chrX:85306871 | T | C | 7 | a0001c0001t0001g0005 a0001c0002t0004g0026 a0001c0002t0004g0027 others(4): Show |
8 | HG00735.hp2 HG02615.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164+292A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 11/16 | chrX | 85306871 | |||||||
| chrX:85307059 | T | C | 3 | a0001c0002t0004g0028 a0001c0002t0006g0159 a0001c0002t0006g0160 |
3 | HG02109.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1164+104A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 11/16 | chrX | 85307059 | |||||||
| chrX:85307112 | C | T | 17 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0052 others(14): Show |
19 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1164+51G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 11/16 | chrX | 85307112 | |||||||
| chrX:85307735 | T | C | 3 | a0001c0002t0004g0028 a0001c0002t0006g0159 a0001c0002t0006g0160 |
3 | HG02109.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1050+389A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 10/16 | chrX | 85307735 | |||||||
| chrX:85307796 | T | G | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1050+328A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 10/16 | chrX | 85307796 | |||||||
| chrX:85307813 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1050+311C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 10/16 | chrX | 85307813 | |||||||
| chrX:85308031 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1050+93A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 10/16 | chrX | 85308031 | |||||||
| chrX:85308226 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.958-10C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85308226 | |||||||
| chrX:85308282 | GT | G | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.958-67delA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85308282 | |||||||
| chrX:85308647 | A | G | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.958-431T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85308647 | |||||||
| chrX:85308653 | C | T | 2 | a0001c0001t0003g0184 a0004c0007t0003g0038 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.958-437G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85308653 | |||||||
| chrX:85308670 | G | T | 1 | a0005c0006t0004g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.958-454C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85308670 | |||||||
| chrX:85308822 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.958-606A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85308822 | |||||||
| chrX:85309093 | C | T | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.958-877G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85309093 | |||||||
| chrX:85309116 | G | A | 1 | a0004c0007t0003g0038 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.958-900C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85309116 | |||||||
| chrX:85309358 | A | C | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.958-1142T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85309358 | |||||||
| chrX:85310377 | A | T | 1 | a0001c0002t0004g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.958-2161T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85310377 | |||||||
| chrX:85310412 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.958-2196T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85310412 | |||||||
| chrX:85310455 | C | G | 1 | a0001c0001t0002g0115 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.958-2239G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85310455 | |||||||
| chrX:85310701 | T | C | 10 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.958-2485A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85310701 | |||||||
| chrX:85310750 | A | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.958-2534T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85310750 | |||||||
| chrX:85310920 | G | A | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.958-2704C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85310920 | |||||||
| chrX:85311231 | C | A | 1 | a0001c0001t0002g0014 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.958-3015G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311231 | |||||||
| chrX:85311245 | C | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.958-3029G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311245 | |||||||
| chrX:85311253 | G | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.958-3037C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311253 | |||||||
| chrX:85311266 | A | G | 1 | a0002c0003t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.958-3050T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311266 | |||||||
| chrX:85311277 | C | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.958-3061G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311277 | |||||||
| chrX:85311349 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.957+3083G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311349 | |||||||
| chrX:85311509 | G | A | 4 | a0001c0002t0004g0045 a0001c0002t0004g0113 a0005c0006t0004g0030 others(1): Show |
4 | HG02615.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+2923C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311509 | |||||||
| chrX:85311726 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.957+2706T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311726 | |||||||
| chrX:85311759 | G | A | 1 | a0002c0003t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.957+2673C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311759 | |||||||
| chrX:85311806 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.957+2626C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85311806 | |||||||
| chrX:85312073 | T | C | 1 | a0001c0001t0001g0013 | 2 | NA18966.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.957+2359A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312073 | |||||||
| chrX:85312130 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.957+2302C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312130 | |||||||
| chrX:85312209 | G | T | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.957+2223C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312209 | |||||||
| chrX:85312396 | T | C | 2 | a0001c0001t0003g0207 a0001c0001t0003g0208 |
2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.957+2036A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312396 | |||||||
| chrX:85312412 | C | A | 35 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(32): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.957+2020G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312412 | |||||||
| chrX:85312695 | T | C | 1 | a0001c0001t0016g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.957+1737A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312695 | |||||||
| chrX:85312707 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.957+1725A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312707 | |||||||
| chrX:85312744 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.957+1688C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312744 | |||||||
| chrX:85312773 | C | A | 1 | a0001c0001t0003g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.957+1659G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312773 | |||||||
| chrX:85312813 | A | C | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.957+1619T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312813 | |||||||
| chrX:85312945 | T | C | 1 | a0002c0003t0001g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.957+1487A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85312945 | |||||||
| chrX:85313046 | A | T | 13 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0171 others(10): Show |
14 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.957+1386T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85313046 | |||||||
| chrX:85313254 | G | A | 10 | a0001c0001t0001g0060 a0001c0002t0004g0019 a0001c0002t0004g0021 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.957+1178C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85313254 | |||||||
| chrX:85313283 | G | T | 2 | a0001c0002t0004g0019 a0001c0002t0004g0021 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.957+1149C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85313283 | |||||||
| chrX:85313364 | T | C | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.957+1068A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85313364 | |||||||
| chrX:85313670 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.957+762G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85313670 | |||||||
| chrX:85313854 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.957+578A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85313854 | |||||||
| chrX:85313944 | G | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.957+488C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85313944 | |||||||
| chrX:85313981 | G | A | 2 | a0001c0002t0004g0045 a0001c0002t0004g0113 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.957+451C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85313981 | |||||||
| chrX:85314037 | T | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.957+395A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85314037 | |||||||
| chrX:85314250 | G | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.957+182C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85314250 | |||||||
| chrX:85314267 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.957+165C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85314267 | |||||||
| chrX:85314295 | C | G | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.957+137G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85314295 | |||||||
| chrX:85314333 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.957+99C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 9/16 | chrX | 85314333 | |||||||
| chrX:85315230 | G | C | 1 | a0001c0001t0002g0147 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.882+477C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 8/16 | chrX | 85315230 | |||||||
| chrX:85315315 | C | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.882+392G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 8/16 | chrX | 85315315 | |||||||
| chrX:85315511 | A | G | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+196T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 8/16 | chrX | 85315511 | |||||||
| chrX:85315675 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.882+32A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 8/16 | chrX | 85315675 | |||||||
| chrX:85315815 | T | A | 2 | a0001c0001t0002g0112 a0001c0001t0009g0085 |
2 | NA18983.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.855-81A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85315815 | |||||||
| chrX:85315913 | T | A | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.855-179A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85315913 | |||||||
| chrX:85316298 | T | C | 1 | a0001c0002t0004g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.855-564A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85316298 | |||||||
| chrX:85316393 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.855-659C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85316393 | |||||||
| chrX:85316461 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.855-727C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85316461 | |||||||
| chrX:85316701 | A | T | 1 | a0001c0002t0004g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.855-967T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85316701 | |||||||
| chrX:85316941 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.855-1207C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85316941 | |||||||
| chrX:85316959 | A | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0103 |
3 | HG01070.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.855-1225T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85316959 | |||||||
| chrX:85316970 | G | A | 1 | a0004c0013t0003g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.855-1236C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85316970 | |||||||
| chrX:85317060 | C | G | 1 | a0001c0002t0004g0166 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.855-1326G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85317060 | |||||||
| chrX:85317088 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.855-1354C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85317088 | |||||||
| chrX:85317247 | T | A | 1 | a0006c0011t0001g0022 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.855-1513A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85317247 | |||||||
| chrX:85317404 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.855-1670G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85317404 | |||||||
| chrX:85317770 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.855-2036C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85317770 | |||||||
| chrX:85317797 | T | C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.855-2063A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85317797 | |||||||
| chrX:85317797 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0060 |
5 | NA18939.hp2 NA18948.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.855-2063A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85317797 | |||||||
| chrX:85318043 | G | A | 3 | a0001c0002t0004g0028 a0001c0002t0006g0159 a0001c0002t0006g0160 |
3 | HG02109.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.855-2309C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318043 | |||||||
| chrX:85318068 | T | A | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.855-2334A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318068 | |||||||
| chrX:85318069 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.855-2335T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318069 | |||||||
| chrX:85318071 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.855-2337T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318071 | |||||||
| chrX:85318225 | A | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.855-2491T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318225 | |||||||
| chrX:85318254 | A | G | 23 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(20): Show |
25 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.855-2520T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318254 | |||||||
| chrX:85318319 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.855-2585T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318319 | |||||||
| chrX:85318622 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.855-2888T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318622 | |||||||
| chrX:85318850 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.855-3116G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318850 | |||||||
| chrX:85318991 | T | A | 1 | a0002c0003t0001g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.855-3257A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85318991 | |||||||
| chrX:85319009 | G | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.855-3275C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319009 | |||||||
| chrX:85319030 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG04228.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.855-3296C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319030 | |||||||
| chrX:85319043 | T | C | 68 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(65): Show |
72 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.855-3309A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319043 | |||||||
| chrX:85319442 | G | C | 4 | a0001c0002t0004g0045 a0001c0002t0004g0113 a0005c0006t0004g0030 others(1): Show |
4 | HG02615.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.855-3708C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319442 | |||||||
| chrX:85319446 | C | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.855-3712G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319446 | |||||||
| chrX:85319704 | C | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.855-3970G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319704 | |||||||
| chrX:85319804 | T | C | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.855-4070A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319804 | |||||||
| chrX:85319937 | A | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0048 |
4 | NA18951.hp1 NA18971.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.855-4203T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319937 | |||||||
| chrX:85319958 | T | A | 1 | a0001c0001t0016g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.855-4224A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85319958 | |||||||
| chrX:85320008 | T | C | 1 | a0002c0003t0001g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.855-4274A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320008 | |||||||
| chrX:85320030 | T | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0103 |
3 | HG01070.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.855-4296A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320030 | |||||||
| chrX:85320069 | C | A | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.855-4335G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320069 | |||||||
| chrX:85320102 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.855-4368C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320102 | |||||||
| chrX:85320228 | C | T | 68 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(65): Show |
72 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.855-4494G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320228 | |||||||
| chrX:85320298 | C | T | 10 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.855-4564G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320298 | |||||||
| chrX:85320510 | C | T | 1 | a0002c0003t0001g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.855-4776G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320510 | |||||||
| chrX:85320517 | T | C | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0045 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.855-4783A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320517 | |||||||
| chrX:85320534 | A | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.855-4800T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320534 | |||||||
| chrX:85320646 | C | T | 1 | a0001c0001t0012g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.855-4912G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320646 | |||||||
| chrX:85320691 | C | G | 49 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0007 others(46): Show |
57 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.855-4957G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320691 | |||||||
| chrX:85320735 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.855-5001G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320735 | |||||||
| chrX:85320792 | C | G | 2 | a0001c0002t0004g0138 a0001c0002t0004g0141 |
2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.855-5058G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320792 | |||||||
| chrX:85320873 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.855-5139A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320873 | |||||||
| chrX:85320953 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.855-5219C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85320953 | |||||||
| chrX:85321004 | A | G | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.855-5270T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321004 | |||||||
| chrX:85321010 | G | C | 68 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(65): Show |
72 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.855-5276C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321010 | |||||||
| chrX:85321028 | T | C | 1 | a0001c0001t0002g0014 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.855-5294A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321028 | |||||||
| chrX:85321082 | A | T | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.855-5348T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321082 | |||||||
| chrX:85321177 | A | T | 8 | a0001c0004t0003g0036 a0001c0004t0003g0198 a0001c0004t0003g0199 others(5): Show |
8 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.855-5443T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321177 | |||||||
| chrX:85321311 | A | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.855-5577T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321311 | |||||||
| chrX:85321336 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.855-5602G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321336 | |||||||
| chrX:85321337 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.855-5603T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321337 | |||||||
| chrX:85321372 | C | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.855-5638G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321372 | |||||||
| chrX:85321505 | T | C | 35 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(32): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.855-5771A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321505 | |||||||
| chrX:85321536 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.855-5802T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321536 | |||||||
| chrX:85321697 | C | T | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.855-5963G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321697 | |||||||
| chrX:85321698 | T | C | 1 | a0004c0007t0003g0038 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.855-5964A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321698 | |||||||
| chrX:85321788 | G | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.855-6054C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321788 | |||||||
| chrX:85321965 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.855-6231G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321965 | |||||||
| chrX:85321969 | C | G | 1 | a0001c0001t0002g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.855-6235G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321969 | |||||||
| chrX:85321974 | T | C | 1 | a0001c0001t0002g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.855-6240A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321974 | |||||||
| chrX:85321978 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.855-6244A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321978 | |||||||
| chrX:85321979 | G | T | 1 | a0001c0001t0002g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.855-6245C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321979 | |||||||
| chrX:85321990 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.855-6256T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321990 | |||||||
| chrX:85321995 | T | A | 9 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.855-6261A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85321995 | |||||||
| chrX:85322031 | T | C | 1 | a0004c0013t0003g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.855-6297A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322031 | |||||||
| chrX:85322047 | C | T | 32 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(29): Show |
35 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.855-6313G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322047 | |||||||
| chrX:85322071 | T | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | NA18955.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.855-6337A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322071 | |||||||
| chrX:85322168 | G | A | 14 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0171 others(11): Show |
15 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.855-6434C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322168 | |||||||
| chrX:85322269 | G | C | 1 | a0001c0001t0002g0047 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.855-6535C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322269 | |||||||
| chrX:85322301 | C | T | 1 | a0002c0003t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.855-6567G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322301 | |||||||
| chrX:85322346 | G | A | 2 | a0001c0001t0001g0177 a0004c0007t0001g0039 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.855-6612C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322346 | |||||||
| chrX:85322387 | T | C | 78 | a0001c0001t0001g0177 a0001c0001t0003g0010 a0001c0001t0003g0011 others(75): Show |
82 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.855-6653A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322387 | |||||||
| chrX:85322388 | C | T | 14 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0171 others(11): Show |
15 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.855-6654G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322388 | |||||||
| chrX:85322429 | A | G | 5 | a0001c0001t0002g0014 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
6 | HG01109.hp1 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.855-6695T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322429 | |||||||
| chrX:85322494 | C | G | 1 | a0001c0002t0004g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.855-6760G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322494 | |||||||
| chrX:85322631 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.855-6897C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322631 | |||||||
| chrX:85322637 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.855-6903G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322637 | |||||||
| chrX:85322707 | C | G | 6 | a0001c0001t0002g0014 a0001c0001t0002g0143 a0001c0001t0002g0153 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.855-6973G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322707 | |||||||
| chrX:85322781 | G | A | 16 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(13): Show |
17 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.855-7047C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85322781 | |||||||
| chrX:85323046 | C | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.855-7312G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323046 | |||||||
| chrX:85323157 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0070 |
2 | HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.855-7423C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323157 | |||||||
| chrX:85323159 | G | T | 1 | a0002c0003t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.855-7425C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323159 | |||||||
| chrX:85323288 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.855-7554A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323288 | |||||||
| chrX:85323362 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.854+7587C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323362 | |||||||
| chrX:85323398 | G | C | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7551C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323398 | |||||||
| chrX:85323399 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7550T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323399 | |||||||
| chrX:85323401 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7548G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323401 | |||||||
| chrX:85323405 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7544G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323405 | |||||||
| chrX:85323406 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7543C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323406 | |||||||
| chrX:85323408 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7541T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323408 | |||||||
| chrX:85323409 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7540G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323409 | |||||||
| chrX:85323411 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7538G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323411 | |||||||
| chrX:85323412 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7537T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323412 | |||||||
| chrX:85323413 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7536C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323413 | |||||||
| chrX:85323414 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.854+7535C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323414 | |||||||
| chrX:85323456 | G | GA | 3 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0124 |
3 | HG02622.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.854+7492dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323456 | |||||||
| chrX:85323497 | A | T | 1 | a0001c0002t0004g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.854+7452T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323497 | |||||||
| chrX:85323551 | T | A | 35 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0001c0002t0004g0021 others(32): Show |
36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.854+7398A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323551 | |||||||
| chrX:85323621 | TA | T | 17 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0052 others(14): Show |
19 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.854+7327delT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323621 | |||||||
| chrX:85323642 | C | G | 4 | a0002c0003t0005g0006 a0002c0003t0005g0088 a0002c0003t0005g0098 others(1): Show |
5 | HG02922.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.854+7307G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323642 | |||||||
| chrX:85323843 | T | C | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0045 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.854+7106A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85323843 | |||||||
| chrX:85324084 | TTGTTGTT others(25): Show |
T | 1 | a0001c0001t0002g0128 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.854+6833_854+6864d others(34): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85324084 | |||||||
| chrX:85324428 | G | T | 2 | a0001c0001t0002g0148 a0001c0001t0002g0197 |
2 | HG01358.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.854+6521C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85324428 | |||||||
| chrX:85324522 | G | T | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.854+6427C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85324522 | |||||||
| chrX:85324636 | T | C | 6 | a0001c0001t0002g0014 a0001c0001t0002g0143 a0001c0001t0002g0153 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.854+6313A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85324636 | |||||||
| chrX:85324707 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.854+6242A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85324707 | |||||||
| chrX:85325006 | C | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0108 a0001c0001t0001g0110 |
3 | HG01169.hp1 HG02300.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.854+5943G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85325006 | |||||||
| chrX:85325056 | G | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.854+5893C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85325056 | |||||||
| chrX:85325466 | T | C | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.854+5483A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85325466 | |||||||
| chrX:85325487 | T | C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.854+5462A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85325487 | |||||||
| chrX:85325547 | T | C | 14 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0171 others(11): Show |
15 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.854+5402A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85325547 | |||||||
| chrX:85325649 | T | G | 3 | a0003c0005t0001g0179 a0003c0005t0001g0180 a0003c0005t0001g0181 |
3 | HG01255.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.854+5300A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85325649 | |||||||
| chrX:85326278 | T | A | 1 | a0001c0001t0002g0133 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.854+4671A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85326278 | |||||||
| chrX:85326281 | CG | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0049 others(14): Show |
19 | HG02132.hp1 HG03017.hp1 HG03490.hp1 others(16): Show |
intron_variant | MODIFIER | c.854+4667delC | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85326281 | |||||||
| chrX:85326353 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.854+4596C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85326353 | |||||||
| chrX:85326392 | G | A | 3 | a0001c0002t0004g0028 a0001c0002t0006g0159 a0001c0002t0006g0160 |
3 | HG02109.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.854+4557C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85326392 | |||||||
| chrX:85326582 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.854+4367C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85326582 | |||||||
| chrX:85327218 | T | C | 78 | a0001c0001t0001g0177 a0001c0001t0003g0010 a0001c0001t0003g0011 others(75): Show |
82 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.854+3731A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85327218 | |||||||
| chrX:85327297 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0109 |
2 | HG00621.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.854+3652G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85327297 | |||||||
| chrX:85327785 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.854+3164A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85327785 | |||||||
| chrX:85328165 | CTTTTTTA others(9): Show |
C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.854+2768_854+2783d others(18): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328165 | |||||||
| chrX:85328168 | T | TTTTA | 11 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0059 others(8): Show |
11 | HG00140.hp1 HG01256.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.854+2777_854+2780d others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328168 | |||||||
| chrX:85328168 | TTTTA | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0017 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.854+2777_854+2780d others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328168 | |||||||
| chrX:85328168 | TTTTATTT others(1): Show |
T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0072 others(56): Show |
66 | HG00438.hp2 HG00673.hp1 HG01255.hp1 others(63): Show |
intron_variant | MODIFIER | c.854+2773_854+2780d others(10): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328168 | |||||||
| chrX:85328168 | TTTTATTT others(9): Show |
T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0152 |
3 | NA18945.hp1 NA18966.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.854+2765_854+2780d others(18): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328168 | |||||||
| chrX:85328220 | T | A | 1 | a0001c0002t0015g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.854+2729A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328220 | |||||||
| chrX:85328298 | G | A | 9 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.854+2651C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328298 | |||||||
| chrX:85328832 | T | TA | 6 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0002g0007 others(3): Show |
7 | HG03491.hp2 HG03492.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+2116dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328832 | |||||||
| chrX:85328846 | AAAAC | A | 10 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.854+2099_854+2102d others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328846 | |||||||
| chrX:85328862 | A | C | 24 | a0001c0001t0001g0111 a0001c0001t0003g0010 a0001c0001t0003g0011 others(21): Show |
26 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.854+2087T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328862 | |||||||
| chrX:85328881 | A | T | 1 | a0001c0001t0003g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.854+2068T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328881 | |||||||
| chrX:85328889 | T | C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.854+2060A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85328889 | |||||||
| chrX:85329054 | CATAGATT | C | 5 | a0001c0001t0002g0017 a0001c0001t0002g0041 a0001c0001t0002g0063 others(2): Show |
5 | HG00408.hp2 HG00621.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.854+1888_854+1894d others(9): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329054 | |||||||
| chrX:85329095 | C | G | 1 | a0002c0003t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.854+1854G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329095 | |||||||
| chrX:85329116 | G | C | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.854+1833C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329116 | |||||||
| chrX:85329536 | C | G | 9 | a0001c0002t0004g0019 a0001c0002t0004g0021 a0001c0002t0004g0138 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.854+1413G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329536 | |||||||
| chrX:85329543 | C | A | 1 | a0001c0009t0002g0144 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.854+1406G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329543 | |||||||
| chrX:85329630 | G | GT | 16 | a0001c0001t0001g0129 a0001c0001t0002g0150 a0001c0001t0003g0207 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.854+1318dupA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329630 | |||||||
| chrX:85329630 | GT | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0146 a0001c0001t0002g0128 others(2): Show |
5 | HG01884.hp2 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.854+1318delA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329630 | |||||||
| chrX:85329644 | T | A | 1 | a0001c0001t0002g0041 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.854+1305A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329644 | |||||||
| chrX:85329644 | TA | T | 11 | a0001c0001t0003g0056 a0001c0001t0003g0184 a0001c0001t0012g0123 others(8): Show |
12 | HG00738.hp1 HG01167.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.854+1304delT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329644 | |||||||
| chrX:85329645 | A | T | 53 | a0001c0001t0001g0081 a0001c0001t0003g0010 a0001c0001t0003g0011 others(50): Show |
56 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.854+1304T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329645 | |||||||
| chrX:85329646 | A | T | 18 | a0001c0001t0013g0167 a0001c0002t0004g0019 a0001c0002t0004g0021 others(15): Show |
19 | HG00738.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.854+1303T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329646 | |||||||
| chrX:85329647 | A | T | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.854+1302T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85329647 | |||||||
| chrX:85330132 | T | C | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.854+817A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85330132 | |||||||
| chrX:85330298 | G | A | 59 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(56): Show |
62 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.854+651C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85330298 | |||||||
| chrX:85330333 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.854+616T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85330333 | |||||||
| chrX:85330655 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.854+294G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 7/16 | chrX | 85330655 | |||||||
| chrX:85331479 | T | C | 1 | a0001c0002t0015g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.724-400A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85331479 | |||||||
| chrX:85331761 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0064 |
2 | HG01070.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.724-682G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85331761 | |||||||
| chrX:85331805 | T | C | 11 | a0001c0002t0004g0016 a0001c0002t0004g0166 a0001c0002t0004g0182 others(8): Show |
12 | HG00673.hp1 HG01981.hp1 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.724-726A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85331805 | |||||||
| chrX:85332199 | C | A | 2 | a0001c0001t0003g0184 a0004c0007t0003g0038 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.724-1120G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85332199 | |||||||
| chrX:85332460 | C | T | 1 | a0001c0009t0002g0144 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.724-1381G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85332460 | |||||||
| chrX:85332599 | C | G | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0045 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.724-1520G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85332599 | |||||||
| chrX:85333373 | C | G | 2 | a0001c0002t0004g0026 a0001c0002t0004g0027 |
2 | HG00735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.724-2294G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85333373 | |||||||
| chrX:85333380 | C | T | 1 | a0003c0005t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.724-2301G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85333380 | |||||||
| chrX:85333410 | A | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.724-2331T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85333410 | |||||||
| chrX:85333693 | G | A | 69 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0043 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.724-2614C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85333693 | |||||||
| chrX:85333956 | G | A | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0045 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.724-2877C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85333956 | |||||||
| chrX:85334111 | A | G | 3 | a0001c0002t0004g0171 a0001c0002t0004g0173 a0001c0002t0004g0174 |
3 | HG01891.hp1 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.724-3032T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85334111 | |||||||
| chrX:85334503 | G | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.724-3424C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85334503 | |||||||
| chrX:85334863 | C | T | 1 | a0001c0001t0003g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.724-3784G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85334863 | |||||||
| chrX:85334888 | C | T | 3 | a0001c0001t0002g0002 a0001c0001t0002g0187 a0001c0001t0002g0188 |
5 | NA18944.hp1 NA18986.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-3809G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85334888 | |||||||
| chrX:85334898 | T | C | 9 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(6): Show |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-3819A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85334898 | |||||||
| chrX:85335475 | A | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0070 |
2 | HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.724-4396T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85335475 | |||||||
| chrX:85335537 | G | GTC | 75 | a0001c0001t0001g0064 a0001c0001t0001g0155 a0001c0001t0001g0170 others(72): Show |
79 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.724-4460_724-4459d others(4): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85335537 | |||||||
| chrX:85335959 | C | CT | 10 | a0001c0001t0003g0163 a0001c0001t0003g0189 a0001c0002t0004g0016 others(7): Show |
11 | HG00673.hp1 HG01981.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.724-4881dupA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85335959 | |||||||
| chrX:85335999 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.724-4920G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85335999 | |||||||
| chrX:85336031 | C | A | 1 | a0001c0001t0002g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.724-4952G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85336031 | |||||||
| chrX:85336146 | T | C | 2 | a0001c0002t0004g0045 a0001c0002t0004g0113 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.724-5067A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85336146 | |||||||
| chrX:85336311 | A | G | 4 | a0001c0001t0003g0184 a0001c0001t0003g0206 a0001c0001t0003g0207 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-5232T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85336311 | |||||||
| chrX:85336513 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.724-5434C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85336513 | |||||||
| chrX:85336870 | C | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0120 a0001c0001t0001g0124 others(3): Show |
6 | HG02132.hp1 NA18961.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.724-5791G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85336870 | |||||||
| chrX:85337185 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.724-6106A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85337185 | |||||||
| chrX:85337645 | T | G | 2 | a0001c0002t0004g0028 a0001c0002t0015g0029 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.724-6566A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85337645 | |||||||
| chrX:85338079 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.724-7000A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85338079 | |||||||
| chrX:85338649 | C | T | 2 | a0001c0002t0004g0045 a0001c0002t0004g0113 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.723+7211G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85338649 | |||||||
| chrX:85338710 | G | C | 3 | a0001c0002t0004g0171 a0001c0002t0004g0173 a0001c0002t0004g0174 |
3 | HG01891.hp1 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.723+7150C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85338710 | |||||||
| chrX:85338786 | T | TA | 18 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(15): Show |
18 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.723+7073dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85338786 | |||||||
| chrX:85339028 | G | GA | 72 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(69): Show |
76 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.723+6831dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85339028 | |||||||
| chrX:85339196 | A | G | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.723+6664T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85339196 | |||||||
| chrX:85339225 | A | T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(15): Show |
18 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.723+6635T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85339225 | |||||||
| chrX:85339376 | G | A | 8 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0185 others(5): Show |
8 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.723+6484C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85339376 | |||||||
| chrX:85339550 | G | A | 1 | a0001c0001t0011g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.723+6310C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85339550 | |||||||
| chrX:85339738 | G | A | 18 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(15): Show |
18 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.723+6122C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85339738 | |||||||
| chrX:85339955 | C | T | 1 | a0001c0002t0006g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.723+5905G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85339955 | |||||||
| chrX:85340063 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.723+5797T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85340063 | |||||||
| chrX:85340540 | C | T | 2 | a0001c0002t0006g0159 a0001c0002t0006g0160 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.723+5320G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85340540 | |||||||
| chrX:85340631 | T | G | 42 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(39): Show |
43 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.723+5229A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85340631 | |||||||
| chrX:85340738 | T | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.723+5122A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85340738 | |||||||
| chrX:85340995 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0084 |
3 | HG02698.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.723+4865T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85340995 | |||||||
| chrX:85341085 | G | A | 76 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(73): Show |
80 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.723+4775C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341085 | |||||||
| chrX:85341090 | A | G | 1 | a0002c0003t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.723+4770T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341090 | |||||||
| chrX:85341092 | G | T | 23 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(20): Show |
23 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.723+4768C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341092 | |||||||
| chrX:85341169 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.723+4691C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341169 | |||||||
| chrX:85341182 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0062 others(6): Show |
11 | HG00438.hp1 HG00609.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.723+4678T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341182 | |||||||
| chrX:85341405 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.723+4455A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341405 | |||||||
| chrX:85341582 | G | T | 1 | a0002c0003t0005g0006 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.723+4278C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341582 | |||||||
| chrX:85341595 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0084 |
3 | HG02698.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.723+4265C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341595 | |||||||
| chrX:85341639 | A | T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(15): Show |
18 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.723+4221T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341639 | |||||||
| chrX:85341648 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.723+4212C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341648 | |||||||
| chrX:85341674 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.723+4186C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341674 | |||||||
| chrX:85341744 | A | G | 1 | a0001c0001t0003g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.723+4116T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341744 | |||||||
| chrX:85341780 | T | G | 4 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(1): Show |
4 | HG00735.hp2 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+4080A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85341780 | |||||||
| chrX:85342025 | C | T | 18 | a0001c0001t0003g0184 a0001c0001t0013g0167 a0001c0004t0003g0015 others(15): Show |
19 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.723+3835G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85342025 | |||||||
| chrX:85342028 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.723+3832G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85342028 | |||||||
| chrX:85342090 | A | G | 1 | a0004c0007t0003g0038 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.723+3770T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85342090 | |||||||
| chrX:85342131 | A | C | 4 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(1): Show |
4 | HG00735.hp2 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+3729T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85342131 | |||||||
| chrX:85342131 | A | T | 72 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(69): Show |
76 | HG00621.hp1 HG00673.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.723+3729T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85342131 | |||||||
| chrX:85342153 | G | A | 2 | a0001c0002t0004g0045 a0001c0002t0004g0113 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.723+3707C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85342153 | |||||||
| chrX:85342649 | T | G | 16 | a0001c0001t0002g0002 a0001c0001t0002g0187 a0001c0001t0002g0188 others(13): Show |
19 | HG00673.hp1 HG01981.hp1 HG03831.hp1 others(16): Show |
intron_variant | MODIFIER | c.723+3211A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85342649 | |||||||
| chrX:85342990 | C | G | 18 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(15): Show |
18 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.723+2870G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85342990 | |||||||
| chrX:85343173 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.723+2687T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85343173 | |||||||
| chrX:85343361 | A | G | 4 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+2499T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85343361 | |||||||
| chrX:85343759 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.723+2101G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85343759 | |||||||
| chrX:85343998 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0086 others(1): Show |
4 | HG01099.hp1 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+1862C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85343998 | |||||||
| chrX:85344323 | A | G | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.723+1537T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85344323 | |||||||
| chrX:85344327 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.723+1533A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85344327 | |||||||
| chrX:85344612 | A | C | 2 | a0001c0002t0004g0016 a0001c0002t0004g0193 |
3 | NA18951.hp2 NA18995.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.723+1248T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85344612 | |||||||
| chrX:85344749 | G | A | 1 | a0001c0002t0004g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.723+1111C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85344749 | |||||||
| chrX:85344789 | A | T | 1 | a0001c0002t0004g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.723+1071T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85344789 | |||||||
| chrX:85344963 | T | A | 71 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(68): Show |
75 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.723+897A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85344963 | |||||||
| chrX:85345375 | C | A | 14 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(11): Show |
14 | HG00621.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.723+485G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85345375 | |||||||
| chrX:85345603 | G | T | 1 | a0001c0001t0002g0042 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.723+257C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 6/16 | chrX | 85345603 | |||||||
| chrX:85346603 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.541-561T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85346603 | |||||||
| chrX:85346717 | T | C | 4 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(1): Show |
4 | HG00735.hp2 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-675A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85346717 | |||||||
| chrX:85347008 | T | G | 18 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(15): Show |
18 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.541-966A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85347008 | |||||||
| chrX:85347066 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.541-1024T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85347066 | |||||||
| chrX:85347410 | C | G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0185 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-1368G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85347410 | |||||||
| chrX:85347607 | T | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(15): Show |
18 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.541-1565A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85347607 | |||||||
| chrX:85347750 | C | T | 1 | a0001c0001t0016g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.541-1708G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85347750 | |||||||
| chrX:85348057 | G | T | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.541-2015C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85348057 | |||||||
| chrX:85348190 | A | G | 1 | a0002c0003t0005g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.541-2148T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85348190 | |||||||
| chrX:85348370 | T | C | 27 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0185 others(24): Show |
30 | HG00673.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.541-2328A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85348370 | |||||||
| chrX:85348468 | C | A | 1 | a0002c0003t0005g0088 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.541-2426G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85348468 | |||||||
| chrX:85348530 | C | T | 20 | a0001c0001t0002g0002 a0001c0001t0002g0187 a0001c0001t0002g0188 others(17): Show |
23 | HG00673.hp1 HG01891.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.541-2488G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85348530 | |||||||
| chrX:85348735 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.540+2615G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85348735 | |||||||
| chrX:85348768 | A | G | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.540+2582T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85348768 | |||||||
| chrX:85349077 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.540+2273C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85349077 | |||||||
| chrX:85349112 | C | T | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.540+2238G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85349112 | |||||||
| chrX:85349218 | A | G | 1 | a0002c0003t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.540+2132T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85349218 | |||||||
| chrX:85349571 | A | G | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.540+1779T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85349571 | |||||||
| chrX:85349760 | G | A | 1 | a0002c0003t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.540+1590C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85349760 | |||||||
| chrX:85349805 | C | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0027 |
2 | HG00735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.540+1545G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85349805 | |||||||
| chrX:85350184 | T | TC | 9 | a0001c0001t0001g0111 a0001c0001t0002g0017 a0001c0001t0002g0048 others(6): Show |
9 | HG00621.hp1 HG01358.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.540+1165dupG | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350184 | |||||||
| chrX:85350330 | A | G | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.540+1020T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350330 | |||||||
| chrX:85350331 | A | G | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.540+1019T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350331 | |||||||
| chrX:85350332 | T | C | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.540+1018A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350332 | |||||||
| chrX:85350427 | T | C | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.540+923A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350427 | |||||||
| chrX:85350495 | G | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.540+855C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350495 | |||||||
| chrX:85350698 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0151 a0001c0001t0003g0010 |
4 | HG03239.hp1 HG03490.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+652T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350698 | |||||||
| chrX:85350793 | T | C | 3 | a0002c0003t0005g0006 a0002c0003t0005g0098 a0002c0003t0005g0101 |
4 | HG02922.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+557A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350793 | |||||||
| chrX:85350956 | G | A | 25 | a0001c0001t0001g0044 a0001c0001t0001g0120 a0001c0001t0001g0122 others(22): Show |
27 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.540+394C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85350956 | |||||||
| chrX:85351116 | C | T | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+234G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85351116 | |||||||
| chrX:85351171 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.540+179T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 5/16 | chrX | 85351171 | |||||||
| chrX:85351781 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439-330C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85351781 | |||||||
| chrX:85351900 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.439-449A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85351900 | |||||||
| chrX:85351908 | AT | A | 35 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(32): Show |
36 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.439-458delA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85351908 | |||||||
| chrX:85352054 | A | G | 21 | a0001c0001t0003g0184 a0001c0001t0003g0206 a0001c0001t0003g0207 others(18): Show |
22 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-603T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85352054 | |||||||
| chrX:85352098 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.439-647A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85352098 | |||||||
| chrX:85352156 | G | A | 1 | a0001c0002t0008g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.439-705C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85352156 | |||||||
| chrX:85352345 | T | C | 14 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(11): Show |
14 | HG00621.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.439-894A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85352345 | |||||||
| chrX:85352510 | T | C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.439-1059A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85352510 | |||||||
| chrX:85352745 | C | T | 1 | a0001c0002t0004g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.439-1294G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85352745 | |||||||
| chrX:85352781 | A | G | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.439-1330T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85352781 | |||||||
| chrX:85353059 | C | T | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.439-1608G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85353059 | |||||||
| chrX:85353465 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.439-2014C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85353465 | |||||||
| chrX:85353575 | C | T | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.439-2124G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85353575 | |||||||
| chrX:85353675 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0060 |
5 | NA18939.hp2 NA18948.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-2224G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85353675 | |||||||
| chrX:85353857 | A | G | 4 | a0001c0002t0004g0028 a0001c0002t0015g0029 a0005c0006t0004g0030 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-2406T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85353857 | |||||||
| chrX:85354017 | G | C | 1 | a0001c0001t0003g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.439-2566C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354017 | |||||||
| chrX:85354231 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.439-2780A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354231 | |||||||
| chrX:85354263 | T | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.439-2812A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354263 | |||||||
| chrX:85354349 | C | T | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.439-2898G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354349 | |||||||
| chrX:85354504 | T | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.439-3053A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354504 | |||||||
| chrX:85354511 | C | T | 8 | a0001c0004t0003g0015 a0001c0004t0003g0036 a0001c0004t0003g0198 others(5): Show |
9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.439-3060G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354511 | |||||||
| chrX:85354515 | C | G | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.439-3064G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354515 | |||||||
| chrX:85354533 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.439-3082C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354533 | |||||||
| chrX:85354728 | T | A | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.439-3277A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354728 | |||||||
| chrX:85354730 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-3279G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354730 | |||||||
| chrX:85354796 | C | G | 1 | a0001c0001t0002g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.439-3345G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354796 | |||||||
| chrX:85354806 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.439-3355C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354806 | |||||||
| chrX:85354940 | G | A | 1 | a0001c0002t0004g0016 | 2 | NA18951.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.439-3489C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85354940 | |||||||
| chrX:85355113 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.439-3662A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355113 | |||||||
| chrX:85355122 | G | A | 1 | a0001c0001t0002g0007 | 2 | NA18953.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.439-3671C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355122 | |||||||
| chrX:85355137 | C | T | 3 | a0001c0002t0004g0171 a0001c0002t0004g0173 a0001c0002t0004g0174 |
3 | HG01891.hp1 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.439-3686G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355137 | |||||||
| chrX:85355165 | T | C | 26 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(23): Show |
26 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.439-3714A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355165 | |||||||
| chrX:85355334 | A | T | 1 | a0001c0001t0002g0063 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.439-3883T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355334 | |||||||
| chrX:85355694 | A | G | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.438+3856T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355694 | |||||||
| chrX:85355702 | GA | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+3847delT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355702 | |||||||
| chrX:85355845 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.438+3705C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355845 | |||||||
| chrX:85355858 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 |
3 | HG02572.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.438+3692C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85355858 | |||||||
| chrX:85356113 | A | G | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.438+3437T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85356113 | |||||||
| chrX:85356176 | G | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.438+3374C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85356176 | |||||||
| chrX:85356322 | G | A | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.438+3228C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85356322 | |||||||
| chrX:85356433 | G | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.438+3117C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85356433 | |||||||
| chrX:85356464 | G | GA | 5 | a0001c0001t0001g0082 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG02145.hp1 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.438+3085dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85356464 | |||||||
| chrX:85356509 | C | T | 1 | a0001c0001t0003g0083 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.438+3041G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85356509 | |||||||
| chrX:85356549 | C | T | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.438+3001G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85356549 | |||||||
| chrX:85356920 | G | A | 1 | a0001c0001t0003g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.438+2630C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85356920 | |||||||
| chrX:85357464 | A | G | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+2086T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85357464 | |||||||
| chrX:85357612 | C | T | 1 | a0001c0002t0004g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.438+1938G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85357612 | |||||||
| chrX:85357640 | C | T | 76 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(73): Show |
80 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.438+1910G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85357640 | |||||||
| chrX:85357818 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.438+1732G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85357818 | |||||||
| chrX:85358180 | A | G | 11 | a0001c0001t0003g0184 a0001c0001t0013g0167 a0001c0004t0003g0015 others(8): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.438+1370T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85358180 | |||||||
| chrX:85358401 | A | G | 2 | a0001c0002t0007g0175 a0001c0002t0007g0176 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.438+1149T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85358401 | |||||||
| chrX:85358496 | C | T | 75 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(72): Show |
79 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.438+1054G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85358496 | |||||||
| chrX:85358866 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.438+684A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85358866 | |||||||
| chrX:85359110 | AACCTTTG others(13): Show |
A | 14 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(11): Show |
14 | HG00621.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.438+420_438+439del others(20): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85359110 | |||||||
| chrX:85359252 | G | A | 4 | a0001c0002t0004g0028 a0001c0002t0015g0029 a0005c0006t0004g0030 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+298C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85359252 | |||||||
| chrX:85359295 | A | G | 18 | a0001c0001t0003g0184 a0001c0001t0013g0167 a0001c0004t0003g0015 others(15): Show |
19 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.438+255T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85359295 | |||||||
| chrX:85359381 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.438+169A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85359381 | |||||||
| chrX:85359385 | T | C | 137 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(134): Show |
149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.438+165A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85359385 | |||||||
| chrX:85359405 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.438+145A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85359405 | |||||||
| chrX:85359425 | A | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0060 |
5 | NA18939.hp2 NA18948.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+125T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85359425 | |||||||
| chrX:85359492 | T | G | 1 | a0001c0001t0002g0042 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.438+58A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 4/16 | chrX | 85359492 | |||||||
| chrX:85360127 | G | T | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.358-497C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360127 | |||||||
| chrX:85360323 | T | C | 44 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(41): Show |
45 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.358-693A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360323 | |||||||
| chrX:85360527 | G | GTA | 19 | a0001c0001t0001g0084 a0001c0001t0001g0129 a0001c0001t0001g0130 others(16): Show |
20 | HG00280.hp1 HG01934.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.358-899_358-898dup others(2): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTATA | 3 | a0001c0001t0002g0133 a0001c0001t0002g0150 a0001c0001t0017g0134 |
3 | NA18982.hp1 NA18989.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.358-901_358-898dup others(4): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTATATAT others(1): Show |
2 | a0001c0001t0003g0135 a0001c0001t0003g0136 |
2 | NA19000.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.358-905_358-898dup others(8): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTATATAT others(9): Show |
1 | a0001c0002t0006g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.358-913_358-898dup others(16): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTATATAT others(13): Show |
1 | a0001c0002t0006g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.358-917_358-898dup others(20): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTATGTAT others(1): Show |
4 | a0001c0004t0003g0200 a0003c0005t0001g0164 a0003c0005t0001g0168 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-898_358-897ins others(8): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTATGTAT others(3): Show |
4 | a0001c0004t0003g0036 a0001c0004t0003g0201 a0001c0004t0003g0202 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-898_358-897ins others(10): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTATGTAT others(5): Show |
3 | a0001c0004t0003g0015 a0001c0004t0003g0203 a0003c0005t0001g0181 |
4 | HG00738.hp1 HG01255.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-898_358-897ins others(12): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTATGTAT others(5): Show |
2 | a0001c0004t0003g0198 a0001c0004t0003g0199 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.358-898_358-897ins others(12): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTGTATAT others(3): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0188 |
4 | NA18986.hp1 NA18994.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-898_358-897ins others(10): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTGTATAT others(5): Show |
2 | a0001c0001t0003g0163 a0001c0001t0003g0189 |
2 | NA19001.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.358-898_358-897ins others(12): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTGTATAT others(7): Show |
2 | a0001c0001t0002g0197 a0001c0002t0004g0190 |
2 | HG00673.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.358-898_358-897ins others(14): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTGTATAT others(9): Show |
3 | a0001c0002t0008g0191 a0001c0002t0008g0192 a0008c0014t0004g0205 |
3 | HG01981.hp1 NA18939.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.358-898_358-897ins others(16): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTGTATAT others(11): Show |
2 | a0001c0002t0004g0193 a0001c0002t0004g0194 |
2 | NA19011.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.358-898_358-897ins others(18): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTGTATAT others(13): Show |
1 | a0001c0002t0004g0016 | 2 | NA18951.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.358-898_358-897ins others(20): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | G | GTGTATAT others(15): Show |
2 | a0001c0002t0004g0195 a0001c0002t0004g0196 |
2 | HG03831.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.358-898_358-897ins others(22): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | GTA | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
52 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.358-899_358-898del others(2): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | GTATATAT others(1): Show |
G | 1 | a0001c0001t0002g0007 | 2 | NA18953.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.358-905_358-898del others(8): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360527 | GTATATAT others(3): Show |
G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0110 |
2 | HG01169.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.358-907_358-898del others(10): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360527 | |||||||
| chrX:85360529 | A | ATG | 2 | a0001c0001t0003g0184 a0001c0001t0013g0167 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.358-900_358-899ins others(2): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360529 | |||||||
| chrX:85360529 | A | G | 1 | a0001c0002t0004g0166 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.358-899T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360529 | |||||||
| chrX:85360531 | A | G | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-901T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360531 | |||||||
| chrX:85360552 | T | C | 1 | a0001c0002t0004g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.358-922A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360552 | |||||||
| chrX:85360554 | T | C | 3 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0166 |
3 | HG00735.hp2 HG06807.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.358-924A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360554 | |||||||
| chrX:85360555 | ATATACAT others(4): Show |
A | 2 | a0001c0002t0004g0027 a0001c0002t0004g0166 |
2 | HG06807.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.358-936_358-926del others(11): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360555 | |||||||
| chrX:85360556 | T | C | 3 | a0001c0002t0004g0026 a0004c0007t0001g0039 a0004c0013t0003g0040 |
3 | HG00735.hp2 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.358-926A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360556 | |||||||
| chrX:85360557 | ATACATAT others(2): Show |
A | 3 | a0001c0002t0004g0026 a0004c0007t0001g0039 a0004c0013t0003g0040 |
3 | HG00735.hp2 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.358-936_358-928del others(9): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360557 | |||||||
| chrX:85360558 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.358-928A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360558 | |||||||
| chrX:85360560 | C | T | 63 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0033 others(60): Show |
67 | HG00621.hp1 HG00673.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.358-930G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360560 | |||||||
| chrX:85360561 | ATATAT | A | 2 | a0001c0001t0001g0032 a0001c0008t0014g0018 |
2 | HG02572.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.358-936_358-932del others(5): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360561 | |||||||
| chrX:85360562 | T | C | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.358-932A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360562 | |||||||
| chrX:85360564 | T | C | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.358-934A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360564 | |||||||
| chrX:85360565 | AT | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.358-936delA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360565 | |||||||
| chrX:85360566 | T | C | 2 | a0001c0002t0004g0171 a0001c0002t0004g0186 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.358-936A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360566 | |||||||
| chrX:85360567 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.358-938_358-937ins others(11): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(8): Show |
1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.358-938_358-937ins others(15): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0170 a0001c0001t0009g0169 a0001c0002t0004g0182 |
3 | HG02258.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.358-938_358-937ins others(13): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0025 a0001c0002t0004g0021 a0001c0002t0007g0176 |
3 | HG01243.hp1 HG02970.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.358-938_358-937ins others(15): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358-938_358-937ins others(15): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0034 a0001c0001t0002g0024 a0001c0002t0010g0035 others(1): Show |
4 | HG01891.hp2 HG03471.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-938_358-937ins others(17): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(12): Show |
6 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0002t0004g0019 others(3): Show |
6 | HG02615.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-938_358-937ins others(19): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(12): Show |
1 | a0001c0002t0004g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.358-938_358-937ins others(19): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0183 a0001c0001t0002g0017 a0001c0002t0004g0142 |
3 | HG00621.hp1 HG02602.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.358-938_358-937ins others(21): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(18): Show |
1 | a0003c0005t0001g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.358-938_358-937ins others(25): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(16): Show |
2 | a0001c0001t0002g0023 a0006c0011t0001g0022 |
2 | HG02071.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.358-938_358-937ins others(23): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.358-938_358-937ins others(25): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360567 | A | C | 10 | a0001c0001t0001g0032 a0001c0001t0003g0206 a0001c0001t0003g0207 others(7): Show |
10 | HG00735.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-937T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360567 | |||||||
| chrX:85360568 | C | CACACACA others(2): Show |
17 | a0001c0001t0003g0184 a0001c0001t0013g0167 a0001c0004t0003g0015 others(14): Show |
18 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.358-939_358-938ins others(9): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360568 | |||||||
| chrX:85360568 | C | CACT | 17 | a0001c0001t0002g0002 a0001c0001t0002g0187 a0001c0001t0002g0188 others(14): Show |
20 | HG00673.hp1 HG01981.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.358-939_358-938ins others(3): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360568 | |||||||
| chrX:85360568 | C | CT | 2 | a0001c0002t0004g0171 a0001c0002t0004g0186 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.358-939_358-938ins others(1): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360568 | |||||||
| chrX:85360568 | C | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(35): Show |
38 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.358-938G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360568 | |||||||
| chrX:85360865 | C | T | 18 | a0001c0001t0003g0184 a0001c0001t0013g0167 a0001c0004t0003g0015 others(15): Show |
19 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.358-1235G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360865 | |||||||
| chrX:85360897 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.358-1267A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85360897 | |||||||
| chrX:85361153 | T | C | 1 | a0001c0001t0016g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.358-1523A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85361153 | |||||||
| chrX:85361702 | T | C | 74 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(71): Show |
78 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.358-2072A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85361702 | |||||||
| chrX:85361831 | T | C | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.358-2201A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85361831 | |||||||
| chrX:85361955 | C | CGT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0034 others(15): Show |
21 | HG00642.hp1 HG01109.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.358-2327_358-2326d others(4): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85361955 | |||||||
| chrX:85361955 | C | CGTGT | 2 | a0001c0002t0004g0028 a0002c0003t0001g0107 |
2 | HG01074.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.358-2329_358-2326d others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85361955 | |||||||
| chrX:85361955 | C | CGTGTGT | 3 | a0001c0001t0001g0033 a0001c0001t0002g0153 a0001c0002t0015g0029 |
3 | HG02622.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.358-2331_358-2326d others(8): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85361955 | |||||||
| chrX:85361955 | CGT | C | 18 | a0001c0001t0001g0087 a0001c0001t0001g0139 a0001c0001t0001g0140 others(15): Show |
18 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.358-2327_358-2326d others(4): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85361955 | |||||||
| chrX:85361955 | CGTGT | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0146 others(26): Show |
30 | HG00621.hp1 HG00738.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.358-2329_358-2326d others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85361955 | |||||||
| chrX:85362327 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.358-2697A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85362327 | |||||||
| chrX:85362699 | C | T | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-3069G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85362699 | |||||||
| chrX:85362968 | G | T | 1 | a0001c0001t0003g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.358-3338C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85362968 | |||||||
| chrX:85363033 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0183 others(8): Show |
11 | HG00621.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-3403A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363033 | |||||||
| chrX:85363366 | TCTGGTTG others(6): Show |
T | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.358-3749_358-3737d others(15): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363366 | |||||||
| chrX:85363381 | T | C | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.358-3751A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363381 | |||||||
| chrX:85363384 | ATGCT | A | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.358-3758_358-3755d others(6): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363384 | |||||||
| chrX:85363389 | A | C | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.358-3759T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363389 | |||||||
| chrX:85363441 | T | C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.358-3811A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363441 | |||||||
| chrX:85363466 | A | G | 1 | a0001c0001t0003g0189 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.358-3836T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363466 | |||||||
| chrX:85363637 | G | A | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358-4007C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363637 | |||||||
| chrX:85363918 | A | G | 18 | a0001c0001t0003g0184 a0001c0001t0013g0167 a0001c0004t0003g0015 others(15): Show |
19 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.357+3774T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363918 | |||||||
| chrX:85363919 | T | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.357+3773A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85363919 | |||||||
| chrX:85364052 | A | T | 1 | a0001c0001t0003g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.357+3640T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85364052 | |||||||
| chrX:85364129 | A | G | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.357+3563T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85364129 | |||||||
| chrX:85364253 | C | G | 25 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(22): Show |
25 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.357+3439G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85364253 | |||||||
| chrX:85364955 | C | A | 2 | a0001c0002t0004g0026 a0001c0002t0004g0027 |
2 | HG00735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.357+2737G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85364955 | |||||||
| chrX:85365086 | T | C | 33 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(30): Show |
33 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.357+2606A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85365086 | |||||||
| chrX:85365110 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.357+2582A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85365110 | |||||||
| chrX:85365244 | C | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.357+2448G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85365244 | |||||||
| chrX:85365320 | T | G | 9 | a0001c0001t0001g0155 a0001c0001t0002g0014 a0001c0001t0002g0143 others(6): Show |
10 | HG01109.hp1 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.357+2372A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85365320 | |||||||
| chrX:85365491 | G | T | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.357+2201C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85365491 | |||||||
| chrX:85365715 | C | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.357+1977G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85365715 | |||||||
| chrX:85366033 | G | C | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.357+1659C>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85366033 | |||||||
| chrX:85366058 | A | G | 1 | a0001c0001t0009g0169 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.357+1634T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85366058 | |||||||
| chrX:85366095 | A | T | 1 | a0002c0003t0005g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.357+1597T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85366095 | |||||||
| chrX:85366126 | A | G | 9 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(6): Show |
9 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.357+1566T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85366126 | |||||||
| chrX:85366184 | G | T | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.357+1508C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85366184 | |||||||
| chrX:85366764 | T | C | 14 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(11): Show |
14 | HG00621.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+928A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85366764 | |||||||
| chrX:85366912 | A | G | 1 | a0001c0002t0004g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.357+780T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85366912 | |||||||
| chrX:85366918 | A | T | 4 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+774T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85366918 | |||||||
| chrX:85367101 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.357+591G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85367101 | |||||||
| chrX:85367102 | G | A | 2 | a0003c0005t0001g0164 a0003c0005t0001g0165 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.357+590C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85367102 | |||||||
| chrX:85367117 | C | A | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.357+575G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85367117 | |||||||
| chrX:85367232 | A | T | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+460T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85367232 | |||||||
| chrX:85367327 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0185 a0001c0001t0009g0169 |
3 | HG02258.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.357+365G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85367327 | |||||||
| chrX:85367440 | T | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0145 |
3 | HG00438.hp1 HG02523.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.357+252A>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85367440 | |||||||
| chrX:85367585 | G | A | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.357+107C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85367585 | |||||||
| chrX:85367624 | A | C | 14 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(11): Show |
14 | HG00621.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+68T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 3/16 | chrX | 85367624 | |||||||
| chrX:85368101 | A | C | 1 | a0001c0002t0004g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283-335T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368101 | |||||||
| chrX:85368121 | ATTTG | A | 4 | a0001c0001t0001g0025 a0001c0001t0002g0017 a0001c0001t0002g0023 others(1): Show |
4 | HG00621.hp1 HG04228.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-359_283-356del others(4): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368121 | |||||||
| chrX:85368389 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.283-623T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368389 | |||||||
| chrX:85368390 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.283-624G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368390 | |||||||
| chrX:85368433 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283-667A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368433 | |||||||
| chrX:85368578 | T | C | 7 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(4): Show |
7 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-812A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368578 | |||||||
| chrX:85368610 | C | A | 2 | a0001c0002t0004g0028 a0001c0002t0015g0029 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.283-844G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368610 | |||||||
| chrX:85368666 | G | A | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.283-900C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368666 | |||||||
| chrX:85368744 | C | T | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283-978G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368744 | |||||||
| chrX:85368915 | G | T | 7 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(4): Show |
7 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1149C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85368915 | |||||||
| chrX:85369143 | C | G | 4 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-1377G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369143 | |||||||
| chrX:85369360 | C | T | 33 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0185 others(30): Show |
36 | HG00673.hp1 HG01255.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.283-1594G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369360 | |||||||
| chrX:85369387 | C | A | 14 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(11): Show |
14 | HG00621.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.283-1621G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369387 | |||||||
| chrX:85369558 | A | G | 1 | a0002c0003t0001g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.283-1792T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369558 | |||||||
| chrX:85369619 | G | T | 10 | a0001c0001t0001g0183 a0001c0001t0003g0184 a0001c0001t0013g0167 others(7): Show |
11 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-1853C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369619 | |||||||
| chrX:85369673 | A | G | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-1907T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369673 | |||||||
| chrX:85369704 | G | A | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283-1938C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369704 | |||||||
| chrX:85369788 | A | G | 1 | a0003c0005t0001g0168 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.283-2022T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369788 | |||||||
| chrX:85369923 | A | G | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.283-2157T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85369923 | |||||||
| chrX:85370147 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.283-2381A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370147 | |||||||
| chrX:85370207 | G | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.283-2441C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370207 | |||||||
| chrX:85370504 | G | A | 17 | a0001c0001t0002g0002 a0001c0001t0002g0187 a0001c0001t0002g0188 others(14): Show |
20 | HG00673.hp1 HG01981.hp1 HG03831.hp1 others(17): Show |
intron_variant | MODIFIER | c.283-2738C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370504 | |||||||
| chrX:85370511 | A | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.283-2745T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370511 | |||||||
| chrX:85370645 | A | G | 27 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(24): Show |
27 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.283-2879T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370645 | |||||||
| chrX:85370672 | A | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | NA18955.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.283-2906T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370672 | |||||||
| chrX:85370929 | A | G | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283-3163T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370929 | |||||||
| chrX:85370961 | A | AT | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.283-3196dupA | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370961 | |||||||
| chrX:85370963 | G | T | 28 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(25): Show |
28 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.283-3197C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85370963 | |||||||
| chrX:85371264 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.283-3498G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85371264 | |||||||
| chrX:85371466 | A | C | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283-3700T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85371466 | |||||||
| chrX:85371502 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.283-3736C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85371502 | |||||||
| chrX:85371833 | G | A | 28 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(25): Show |
28 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.283-4067C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85371833 | |||||||
| chrX:85371884 | A | G | 42 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0185 others(39): Show |
46 | HG00673.hp1 HG00738.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.283-4118T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85371884 | |||||||
| chrX:85372200 | C | G | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.283-4434G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372200 | |||||||
| chrX:85372212 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.283-4446G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372212 | |||||||
| chrX:85372241 | G | A | 1 | a0008c0014t0004g0205 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.283-4475C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372241 | |||||||
| chrX:85372285 | C | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.283-4519G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372285 | |||||||
| chrX:85372312 | C | T | 2 | a0003c0005t0001g0164 a0003c0005t0001g0165 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.283-4546G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372312 | |||||||
| chrX:85372316 | G | T | 1 | a0002c0003t0001g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283-4550C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372316 | |||||||
| chrX:85372343 | C | CA | 25 | a0001c0001t0001g0151 a0001c0001t0001g0183 a0001c0001t0001g0185 others(22): Show |
26 | HG00735.hp2 HG00738.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-4578dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372343 | |||||||
| chrX:85372343 | C | CAA | 11 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0002g0017 others(8): Show |
11 | HG00621.hp1 HG01243.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-4579_283-4578d others(4): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372343 | |||||||
| chrX:85372343 | C | CAAA | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0002t0010g0035 others(2): Show |
5 | HG01891.hp2 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-4580_283-4578d others(5): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372343 | |||||||
| chrX:85372343 | CA | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
58 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.283-4578delT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372343 | |||||||
| chrX:85372669 | C | T | 2 | a0001c0001t0003g0052 a0001c0001t0003g0053 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.283-4903G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372669 | |||||||
| chrX:85372772 | A | ATATATAT others(10): Show |
1 | a0001c0001t0003g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283-5007_283-5006i others(19): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372772 | |||||||
| chrX:85372772 | A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0206 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.283-5007_283-5006i others(23): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372772 | |||||||
| chrX:85372772 | A | ATATATAT others(20): Show |
1 | a0001c0001t0003g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.283-5007_283-5006i others(29): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372772 | |||||||
| chrX:85372773 | C | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.283-5007G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372773 | |||||||
| chrX:85372773 | C | CTA | 2 | a0001c0001t0001g0013 a0001c0001t0001g0152 |
3 | NA18945.hp1 NA18966.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.283-5009_283-5008d others(4): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372773 | |||||||
| chrX:85372773 | C | CTATATAT others(17): Show |
1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283-5008_283-5007i others(26): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372773 | |||||||
| chrX:85372910 | T | C | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.283-5144A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85372910 | |||||||
| chrX:85373317 | G | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.283-5551C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373317 | |||||||
| chrX:85373388 | A | G | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.283-5622T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373388 | |||||||
| chrX:85373480 | T | A | 2 | a0005c0006t0004g0030 a0005c0006t0004g0031 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.282+5693A>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373480 | |||||||
| chrX:85373536 | T | C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.282+5637A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373536 | |||||||
| chrX:85373631 | T | C | 16 | a0001c0001t0002g0002 a0001c0001t0002g0187 a0001c0001t0002g0188 others(13): Show |
19 | HG00673.hp1 HG01981.hp1 HG03831.hp1 others(16): Show |
intron_variant | MODIFIER | c.282+5542A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373631 | |||||||
| chrX:85373651 | C | T | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.282+5522G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373651 | |||||||
| chrX:85373665 | A | G | 1 | a0001c0001t0013g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.282+5508T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373665 | |||||||
| chrX:85373810 | T | C | 6 | a0001c0001t0001g0155 a0001c0001t0002g0014 a0001c0001t0002g0153 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+5363A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373810 | |||||||
| chrX:85373950 | T | C | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.282+5223A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85373950 | |||||||
| chrX:85374145 | A | C | 1 | a0001c0002t0004g0166 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.282+5028T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85374145 | |||||||
| chrX:85374146 | G | T | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.282+5027C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85374146 | |||||||
| chrX:85374318 | C | A | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.282+4855G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85374318 | |||||||
| chrX:85374547 | T | C | 2 | a0004c0007t0001g0039 a0004c0013t0003g0040 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.282+4626A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85374547 | |||||||
| chrX:85374885 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.282+4288T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85374885 | |||||||
| chrX:85374991 | G | T | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+4182C>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85374991 | |||||||
| chrX:85375023 | C | A | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.282+4150G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375023 | |||||||
| chrX:85375028 | C | A | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.282+4145G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375028 | |||||||
| chrX:85375080 | A | G | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.282+4093T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375080 | |||||||
| chrX:85375163 | T | C | 1 | a0001c0001t0003g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.282+4010A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375163 | |||||||
| chrX:85375175 | C | CA | 7 | a0001c0004t0003g0198 a0001c0004t0003g0199 a0001c0004t0003g0200 others(4): Show |
7 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+3997dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375175 | |||||||
| chrX:85375509 | C | T | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+3664G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375509 | |||||||
| chrX:85375645 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.282+3528T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375645 | |||||||
| chrX:85375821 | T | C | 1 | a0001c0008t0014g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.282+3352A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375821 | |||||||
| chrX:85375976 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(17): Show |
20 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.282+3197C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85375976 | |||||||
| chrX:85376002 | C | T | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.282+3171G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376002 | |||||||
| chrX:85376126 | A | T | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.282+3047T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376126 | |||||||
| chrX:85376143 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.282+3030T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376143 | |||||||
| chrX:85376227 | G | A | 2 | a0001c0002t0006g0159 a0001c0002t0006g0160 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.282+2946C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376227 | |||||||
| chrX:85376507 | C | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
5 | HG01261.hp1 NA18951.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+2666G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376507 | |||||||
| chrX:85376535 | C | G | 1 | a0001c0001t0003g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.282+2638G>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376535 | |||||||
| chrX:85376570 | A | G | 1 | a0001c0002t0004g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.282+2603T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376570 | |||||||
| chrX:85376579 | A | G | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.282+2594T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376579 | |||||||
| chrX:85376595 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.282+2578T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376595 | |||||||
| chrX:85376779 | G | A | 2 | a0003c0005t0001g0164 a0003c0005t0001g0165 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.282+2394C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376779 | |||||||
| chrX:85376794 | A | G | 2 | a0003c0005t0001g0164 a0003c0005t0001g0165 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.282+2379T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376794 | |||||||
| chrX:85376841 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.282+2332A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376841 | |||||||
| chrX:85376867 | A | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(11): Show |
14 | HG00621.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+2306T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376867 | |||||||
| chrX:85376933 | A | AAAAAC | 3 | a0004c0007t0001g0039 a0004c0007t0003g0038 a0004c0013t0003g0040 |
3 | HG02055.hp1 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.282+2235_282+2239d others(7): Show |
POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85376933 | |||||||
| chrX:85377118 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.282+2055T>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85377118 | |||||||
| chrX:85377336 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.282+1837G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85377336 | |||||||
| chrX:85377497 | C | T | 1 | a0001c0001t0003g0163 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.282+1676G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85377497 | |||||||
| chrX:85377814 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.282+1359C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85377814 | |||||||
| chrX:85377829 | T | C | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0028 others(3): Show |
6 | HG00735.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+1344A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85377829 | |||||||
| chrX:85377855 | T | C | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+1318A>G | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85377855 | |||||||
| chrX:85378094 | G | A | 73 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(70): Show |
77 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.282+1079C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85378094 | |||||||
| chrX:85378143 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.282+1030C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85378143 | |||||||
| chrX:85378324 | C | T | 1 | a0001c0002t0004g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.282+849G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85378324 | |||||||
| chrX:85378336 | A | T | 1 | a0001c0001t0002g0042 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.282+837T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85378336 | |||||||
| chrX:85378371 | T | TA | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+801dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85378371 | |||||||
| chrX:85378578 | C | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01891.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+595G>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85378578 | |||||||
| chrX:85378605 | C | T | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+568G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85378605 | |||||||
| chrX:85378829 | A | G | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+344T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85378829 | |||||||
| chrX:85379053 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.282+120T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85379053 | |||||||
| chrX:85379055 | A | G | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+118T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 2/16 | chrX | 85379055 | |||||||
| chrX:85379512 | G | A | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-41-17C>T | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 1/16 | chrX | 85379512 | |||||||
| chrX:85379533 | A | G | 28 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0032 others(25): Show |
28 | HG00621.hp1 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-41-38T>C | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 1/16 | chrX | 85379533 | |||||||
| chrX:85379558 | C | T | 3 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-41-63G>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 1/16 | chrX | 85379558 | |||||||
| chrX:85379584 | A | T | 1 | a0001c0001t0002g0017 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-42+55T>A | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 1/16 | chrX | 85379584 | |||||||
| chrX:85379595 | C | CA | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+43dupT | POF1B | ENSG00000124429.18 | transcript | ENST00000262753.9 | protein_coding | 1/16 | chrX | 85379595 |