Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 59350 |
| ensemblid | ENSG00000171509.16 |
| hgncid | 19718 |
| symbol | RXFP1 |
| name | relaxin family peptide receptor 1 |
| refseq_nuc | NM_021634.4 |
| refseq_prot | NP_067647.2 |
| ensembl_nuc | ENST00000307765.10 |
| ensembl_prot | ENSP00000303248.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 158521882 |
| end | 158653372 |
| strand | + |
| ver | v1.2 |
| region | chr4:158521882-158653372 |
| region5000 | chr4:158516882-158658372 |
| regionname0 | RXFP1_chr4_158521882_158653372 |
| regionname5000 | RXFP1_chr4_158516882_158658372 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 757 | 202 | 81 | 41 | 47 | 10 | 21 | 38 | RXFP1_chr4_158516882_158658372 | RXFP1 | MTSGS others(752): Show |
chr4 | 158516882 | 158658372 |
| a0002 | 0/0 | 757 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | MTSGS others(752): Show |
chr4 | 158516882 | 158658372 |
| a0003 | 0/0 | 757 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | MTSGS others(752): Show |
chr4 | 158516882 | 158658372 |
| a0004 | 0/0 | 757 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | MTSGS others(752): Show |
chr4 | 158516882 | 158658372 |
| a0005 | 0/0 | 757 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | MTSGS others(752): Show |
chr4 | 158516882 | 158658372 |
| a0006 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | MTSGS others(752): Show |
chr4 | 158516882 | 158658372 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2271 | 202 | 81 | 41 | 47 | 10 | 21 | RXFP1_chr4_158516882_158658372 | RXFP1 | ATGAC others(2266): Show |
chr4 | 158516882 | 158658372 | ||
| a0002c0002 | 0/0 | 2271 | 3 | 0 | 0 | 0 | 0 | 3 | RXFP1_chr4_158516882_158658372 | RXFP1 | ATGAC others(2266): Show |
chr4 | 158516882 | 158658372 | ||
| a0003c0003 | 0/0 | 2271 | 2 | 2 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | ATGAC others(2266): Show |
chr4 | 158516882 | 158658372 | ||
| a0004c0006 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | ATGAC others(2266): Show |
chr4 | 158516882 | 158658372 | ||
| a0005c0004 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | ATGAC others(2266): Show |
chr4 | 158516882 | 158658372 | ||
| a0006c0005 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | ATGAC others(2266): Show |
chr4 | 158516882 | 158658372 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3686 | 185 | 67 | 40 | 45 | 10 | 21 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3681): Show |
chr4 | 158516882 | 158658372 |
| a0001c0001t0002 | 0/0 | 3683 | 6 | 6 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3678): Show |
chr4 | 158516882 | 158658372 |
| a0001c0001t0003 | 0/0 | 3686 | 5 | 4 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3681): Show |
chr4 | 158516882 | 158658372 |
| a0001c0001t0004 | 0/0 | 3688 | 4 | 4 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3683): Show |
chr4 | 158516882 | 158658372 |
| a0001c0001t0005 | 0/0 | 3686 | 2 | 0 | 0 | 2 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3681): Show |
chr4 | 158516882 | 158658372 |
| a0002c0002t0001 | 0/0 | 3686 | 3 | 0 | 0 | 0 | 0 | 3 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3681): Show |
chr4 | 158516882 | 158658372 |
| a0003c0003t0001 | 0/0 | 3686 | 2 | 2 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3681): Show |
chr4 | 158516882 | 158658372 |
| a0004c0006t0001 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3681): Show |
chr4 | 158516882 | 158658372 |
| a0005c0004t0001 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3681): Show |
chr4 | 158516882 | 158658372 |
| a0006c0005t0002 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | AGAAA others(3678): Show |
chr4 | 158516882 | 158658372 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0003c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0003c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0004c0006t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0005c0004t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0006c0005t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00438 | hp1 | a0004 | c0006 | t0001 | g0076 | EAS | CHS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01071 | hp2 | a0005 | c0004 | t0001 | g0120 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0102 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0103 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19030 | hp2 | a0006 | c0005 | t0002 | g0207 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ASW | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | ASW | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | USA | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | USA | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0094 | REF | REF | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0200 | REF | REF | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158617147 | G | A | 1 | a0003 | 2 | HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.697G>A | p.Val233Ile | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/18 | 792/3686 | 697/2274 | 233/757 | chr4 | 158617147 | |||
| chr4:158628679 | C | T | 1 | a0004 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.869C>T | p.Thr290Ile | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/18 | 964/3686 | 869/2274 | 290/757 | chr4 | 158628679 | |||
| chr4:158645088 | A | T | 1 | a0002 | 3 | HG02735.hp2 HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.1295A>T | p.Tyr432Phe | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/18 | 1390/3686 | 1295/2274 | 432/757 | chr4 | 158645088 | |||
| chr4:158647070 | T | C | 1 | a0005 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.1625T>C | p.Val542Ala | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/18 | 1720/3686 | 1625/2274 | 542/757 | chr4 | 158647070 | |||
| chr4:158651901 | G | A | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2120G>A | p.Ser707Asn | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 18/18 | 2215/3686 | 2120/2274 | 707/757 | chr4 | 158651901 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158521909 | G | A | 1 | a0001c0001t0003 | 5 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-68G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/18 | 68 | chr4 | 158521909 | ||||||
| chr4:158652274 | TAAG | T | 2 | a0001c0001t0002 a0006c0005t0002 |
7 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*221_*223delAGA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 18/18 | 221 | INFO_REALIGN_3_PRIME | chr4 | 158652274 | |||||
| chr4:158652593 | A | G | 1 | a0001c0001t0005 | 2 | NA18993.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*538A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 18/18 | 538 | chr4 | 158652593 | ||||||
| chr4:158653362 | A | ACT | 1 | a0001c0001t0004 | 4 | HG02258.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1308_*1309dupCT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 18/18 | 1310 | INFO_REALIGN_3_PRIME | chr4 | 158653362 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158522226 | T | C | 3 | a0001c0001t0001g0004 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.49+201T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158522226 | |||||||
| chr4:158522232 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(154): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.49+207G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158522232 | |||||||
| chr4:158522291 | T | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(154): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.49+266T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158522291 | |||||||
| chr4:158522675 | T | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
22 | HG00558.hp1 HG00639.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.49+650T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158522675 | |||||||
| chr4:158522927 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.49+902T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158522927 | |||||||
| chr4:158523143 | T | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
22 | HG00558.hp1 HG00639.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.49+1118T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158523143 | |||||||
| chr4:158523162 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0161 others(37): Show |
42 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.49+1137T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158523162 | |||||||
| chr4:158523438 | A | T | 5 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0004g0204 others(2): Show |
5 | HG03139.hp2 HG03486.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+1413A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158523438 | |||||||
| chr4:158523452 | C | G | 46 | a0001c0001t0001g0029 a0001c0001t0001g0117 a0001c0001t0001g0118 others(43): Show |
46 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.49+1427C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158523452 | |||||||
| chr4:158523728 | C | T | 48 | a0001c0001t0001g0029 a0001c0001t0001g0117 a0001c0001t0001g0118 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.49+1703C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158523728 | |||||||
| chr4:158523874 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02723.hp1 HG03516.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+1849C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158523874 | |||||||
| chr4:158523876 | T | C | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
23 | HG00558.hp1 HG00639.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.49+1851T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158523876 | |||||||
| chr4:158524076 | G | C | 1 | a0001c0001t0003g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.49+2051G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158524076 | |||||||
| chr4:158524164 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.49+2139T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158524164 | |||||||
| chr4:158524241 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(69): Show |
74 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.49+2216A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158524241 | |||||||
| chr4:158524245 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(35): Show |
40 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.49+2220C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158524245 | |||||||
| chr4:158524787 | T | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+2762T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158524787 | |||||||
| chr4:158524844 | T | TTTAC | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+2822_49+2823ins others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158524844 | ||||||
| chr4:158524939 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0198 |
2 | HG02109.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.49+2914C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158524939 | |||||||
| chr4:158524940 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.49+2915G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158524940 | |||||||
| chr4:158524973 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.49+2948C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158524973 | |||||||
| chr4:158525063 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+3038G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525063 | |||||||
| chr4:158525202 | C | T | 4 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+3177C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525202 | |||||||
| chr4:158525209 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG02615.hp1 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+3184T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525209 | |||||||
| chr4:158525219 | C | CG | 91 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.49+3203dupG | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158525219 | ||||||
| chr4:158525225 | G | C | 3 | a0001c0001t0001g0199 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG02615.hp1 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+3200G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525225 | |||||||
| chr4:158525291 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+3266G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525291 | |||||||
| chr4:158525316 | T | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+3291T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525316 | |||||||
| chr4:158525332 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0004g0204 others(4): Show |
7 | HG02615.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+3307G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525332 | |||||||
| chr4:158525469 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+3444C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525469 | |||||||
| chr4:158525502 | A | G | 15 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(12): Show |
15 | HG02258.hp1 HG02280.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+3477A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525502 | |||||||
| chr4:158525658 | T | C | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.49+3633T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525658 | |||||||
| chr4:158525926 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.49+3901A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158525926 | |||||||
| chr4:158526347 | A | G | 2 | a0001c0001t0002g0115 a0001c0001t0002g0181 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.49+4322A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526347 | |||||||
| chr4:158526384 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01123.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.49+4359A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526384 | |||||||
| chr4:158526507 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.49+4482G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526507 | |||||||
| chr4:158526527 | A | G | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+4502A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526527 | |||||||
| chr4:158526579 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+4554G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526579 | |||||||
| chr4:158526665 | T | C | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+4640T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526665 | |||||||
| chr4:158526777 | A | AATC | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.49+4754_49+4756dup others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158526777 | ||||||
| chr4:158526820 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.49+4795C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526820 | |||||||
| chr4:158526855 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.49+4830C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526855 | |||||||
| chr4:158526875 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49+4850T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526875 | |||||||
| chr4:158526932 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.49+4907C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158526932 | |||||||
| chr4:158527105 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.49+5080A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527105 | |||||||
| chr4:158527117 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.49+5092A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527117 | |||||||
| chr4:158527309 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.49+5284G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527309 | |||||||
| chr4:158527390 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.49+5365G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527390 | |||||||
| chr4:158527416 | G | A | 7 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01123.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+5391G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527416 | |||||||
| chr4:158527417 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.49+5392T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527417 | |||||||
| chr4:158527547 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02723.hp1 HG03516.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+5522C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527547 | |||||||
| chr4:158527560 | A | AATATATA others(19): Show |
1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.49+5536_49+5537ins others(26): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527560 | ||||||
| chr4:158527562 | A | AATATATA others(5): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02486.hp1 HG03471.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.49+5538_49+5539ins others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527562 | ||||||
| chr4:158527562 | A | AATATATA others(17): Show |
1 | a0001c0001t0001g0193 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49+5538_49+5539ins others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527562 | ||||||
| chr4:158527562 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.49+5537A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527562 | |||||||
| chr4:158527564 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+5540_49+5541ins others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+5540_49+5541ins others(19): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAAAAA others(5): Show |
3 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG01168.hp1 NA18993.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAAAAT others(4): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02129.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(11): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAAAAT others(16): Show |
2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(23): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAAATA others(5): Show |
37 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(34): Show |
37 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAAATA others(7): Show |
1 | a0001c0001t0001g0046 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+5540_49+5541ins others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAAATA others(11): Show |
2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(18): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAAATA others(15): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG02615.hp1 HG03516.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(22): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAATAT others(4): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG01517.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(11): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0001g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.49+5540_49+5541ins others(13): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAAT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAATATA others(5): Show |
43 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(40): Show |
43 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAATATA others(7): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0077 others(5): Show |
9 | HG00140.hp1 HG00280.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAATATA others(9): Show |
2 | a0001c0001t0001g0206 a0006c0005t0002g0207 |
2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAATATA others(11): Show |
3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02129.hp1 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(18): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAAATATA others(13): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.49+5540_49+5541ins others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAATATAT others(4): Show |
1 | a0001c0001t0001g0182 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.49+5540_49+5541ins others(11): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0131 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.49+5540_49+5541ins others(13): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.49+5544_49+5553dup others(10): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AATATATA others(5): Show |
31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0097 others(28): Show |
32 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.49+5542_49+5553dup others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AATATATA others(7): Show |
6 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0095 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+5540_49+5553dup others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49+5553_49+5554ins others(22): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158527564 | ||||||
| chr4:158527564 | A | AT | 3 | a0001c0001t0001g0002 a0001c0001t0001g0179 a0001c0001t0001g0180 |
4 | HG01884.hp1 HG02280.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+5539_49+5540ins others(1): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527564 | |||||||
| chr4:158527564 | A | ATAT | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+5539_49+5540ins others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527564 | |||||||
| chr4:158527564 | A | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0105 a0001c0001t0001g0108 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.49+5539A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527564 | |||||||
| chr4:158527566 | T | A | 1 | a0001c0001t0003g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.49+5541T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527566 | |||||||
| chr4:158527576 | T | G | 1 | a0004c0006t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.49+5551T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527576 | |||||||
| chr4:158527577 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+5552A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527577 | |||||||
| chr4:158527579 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.49+5554G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527579 | |||||||
| chr4:158527677 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+5652G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527677 | |||||||
| chr4:158527805 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.49+5780C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527805 | |||||||
| chr4:158527970 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+5945G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158527970 | |||||||
| chr4:158528357 | T | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.49+6332T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158528357 | |||||||
| chr4:158528399 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.49+6374G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158528399 | |||||||
| chr4:158528569 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.49+6544C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158528569 | |||||||
| chr4:158528704 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+6679T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158528704 | |||||||
| chr4:158528853 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.49+6828T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158528853 | |||||||
| chr4:158528891 | C | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.49+6866C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158528891 | |||||||
| chr4:158528960 | C | T | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.49+6935C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158528960 | |||||||
| chr4:158529087 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+7062G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158529087 | |||||||
| chr4:158529240 | G | GTTTT | 87 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.49+7218_49+7221dup others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158529240 | ||||||
| chr4:158529244 | T | TTTG | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+7246_49+7248dup others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158529244 | ||||||
| chr4:158529244 | T | TTTGTTG | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+7243_49+7248dup others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158529244 | ||||||
| chr4:158529244 | T | TTTGTTGT others(5): Show |
1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.49+7237_49+7248dup others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158529244 | ||||||
| chr4:158529244 | T | TTTTG | 3 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0118 |
3 | HG00741.hp1 HG02602.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49+7221_49+7222ins others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158529244 | ||||||
| chr4:158529244 | TTTG | T | 7 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01123.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+7246_49+7248del others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158529244 | ||||||
| chr4:158529244 | TTTGTTG | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(63): Show |
67 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.49+7243_49+7248del others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158529244 | ||||||
| chr4:158529247 | G | T | 20 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0067 others(17): Show |
20 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.49+7222G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158529247 | |||||||
| chr4:158529265 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(63): Show |
67 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.49+7240G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158529265 | |||||||
| chr4:158529364 | TCCTC | T | 3 | a0003c0003t0001g0005 a0003c0003t0001g0006 a0006c0005t0002g0207 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49+7342_49+7345del others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158529364 | ||||||
| chr4:158529365 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.49+7340C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158529365 | |||||||
| chr4:158529392 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01099.hp1 HG01255.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.49+7367G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158529392 | |||||||
| chr4:158529392 | G | T | 1 | a0006c0005t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.49+7367G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158529392 | |||||||
| chr4:158529503 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02129.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.49+7478G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158529503 | |||||||
| chr4:158529523 | T | A | 1 | a0001c0001t0001g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+7498T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158529523 | |||||||
| chr4:158530072 | T | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.49+8047T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530072 | |||||||
| chr4:158530303 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+8278T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530303 | |||||||
| chr4:158530614 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.49+8589A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530614 | |||||||
| chr4:158530619 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.49+8594T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530619 | |||||||
| chr4:158530702 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.49+8677A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530702 | |||||||
| chr4:158530750 | T | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+8725T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530750 | |||||||
| chr4:158530810 | C | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.49+8785C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530810 | |||||||
| chr4:158530966 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.49+8941T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530966 | |||||||
| chr4:158531160 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+9135C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158531160 | |||||||
| chr4:158531656 | A | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.49+9631A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158531656 | |||||||
| chr4:158531737 | T | C | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.49+9712T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158531737 | |||||||
| chr4:158531916 | GTATT | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.49+9893_49+9896del others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158531916 | ||||||
| chr4:158531919 | TTTTG | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.49+9922_49+9925del others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158531919 | ||||||
| chr4:158531923 | G | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.49+9898G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158531923 | |||||||
| chr4:158531932 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.49+9907T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158531932 | |||||||
| chr4:158531998 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.49+9973T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158531998 | |||||||
| chr4:158532145 | A | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+10120A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158532145 | |||||||
| chr4:158532193 | TG | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+10169delG | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158532193 | |||||||
| chr4:158532231 | G | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+10206G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158532231 | |||||||
| chr4:158532614 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+10589C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158532614 | |||||||
| chr4:158533127 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.49+11102A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158533127 | |||||||
| chr4:158533281 | T | G | 2 | a0001c0001t0002g0115 a0001c0001t0002g0181 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.49+11256T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158533281 | |||||||
| chr4:158533492 | C | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+11467C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158533492 | |||||||
| chr4:158533630 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.49+11605T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158533630 | |||||||
| chr4:158533879 | A | G | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+11854A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158533879 | |||||||
| chr4:158534063 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.49+12038G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158534063 | |||||||
| chr4:158534245 | A | AT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0196 others(3): Show |
6 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+12239dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158534245 | ||||||
| chr4:158534245 | AT | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0040 others(51): Show |
55 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+12239delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158534245 | ||||||
| chr4:158534245 | ATT | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01081.hp1 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+12238_49+12239d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158534245 | ||||||
| chr4:158534245 | ATTT | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.49+12237_49+12239d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158534245 | ||||||
| chr4:158534297 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+12272G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158534297 | |||||||
| chr4:158534341 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+12316G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158534341 | |||||||
| chr4:158534489 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | HG00642.hp1 HG01081.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.49+12464C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158534489 | |||||||
| chr4:158534706 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.49+12681T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158534706 | |||||||
| chr4:158534860 | ATATATTA others(5): Show |
A | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.49+12852_49+12863d others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158534860 | ||||||
| chr4:158534885 | TATA | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(61): Show |
65 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.49+12865_49+12867d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158534885 | ||||||
| chr4:158534908 | T | TATA | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.49+12888_49+12890d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158534908 | ||||||
| chr4:158534996 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+12971A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158534996 | |||||||
| chr4:158535031 | C | T | 13 | a0001c0001t0001g0068 a0001c0001t0001g0195 a0001c0001t0001g0196 others(10): Show |
13 | HG01123.hp1 HG01261.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.49+13006C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158535031 | |||||||
| chr4:158535032 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+13007G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158535032 | |||||||
| chr4:158535140 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.49+13115G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158535140 | |||||||
| chr4:158535209 | G | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.49+13184G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158535209 | |||||||
| chr4:158535813 | C | G | 3 | a0002c0002t0001g0101 a0002c0002t0001g0102 a0002c0002t0001g0103 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.49+13788C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158535813 | |||||||
| chr4:158535876 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.49+13851C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158535876 | |||||||
| chr4:158536223 | T | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+14198T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158536223 | |||||||
| chr4:158536375 | T | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.49+14350T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158536375 | |||||||
| chr4:158536435 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+14410G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158536435 | |||||||
| chr4:158536869 | A | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.49+14844A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158536869 | |||||||
| chr4:158536883 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.49+14858G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158536883 | |||||||
| chr4:158536975 | A | C | 1 | a0001c0001t0001g0192 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.49+14950A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158536975 | |||||||
| chr4:158537016 | GT | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+14994delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158537016 | ||||||
| chr4:158537099 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.49+15074T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158537099 | |||||||
| chr4:158537137 | G | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.49+15112G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158537137 | |||||||
| chr4:158537208 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.49+15183G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158537208 | |||||||
| chr4:158537304 | T | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+15279T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158537304 | |||||||
| chr4:158537444 | G | T | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.49+15419G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158537444 | |||||||
| chr4:158537448 | A | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+15423A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158537448 | |||||||
| chr4:158537473 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.49+15448A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158537473 | |||||||
| chr4:158537773 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+15748A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158537773 | |||||||
| chr4:158538049 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+16024A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158538049 | |||||||
| chr4:158538059 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.49+16034A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158538059 | |||||||
| chr4:158538125 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+16100T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158538125 | |||||||
| chr4:158538430 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.49+16405C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158538430 | |||||||
| chr4:158538707 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0082 a0001c0001t0001g0159 |
3 | HG00639.hp2 HG02647.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49+16682G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158538707 | |||||||
| chr4:158538760 | C | T | 60 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.49+16735C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158538760 | |||||||
| chr4:158538804 | CAA | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0097 others(8): Show |
12 | HG02129.hp1 HG02723.hp1 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+16796_49+16797d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158538804 | ||||||
| chr4:158538804 | CAAA | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0032 others(62): Show |
65 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.49+16795_49+16797d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158538804 | ||||||
| chr4:158538839 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+16814G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158538839 | |||||||
| chr4:158539249 | C | T | 19 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0195 others(16): Show |
19 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.49+17224C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539249 | |||||||
| chr4:158539265 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02615.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.49+17240G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539265 | |||||||
| chr4:158539337 | G | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.49+17312G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539337 | |||||||
| chr4:158539338 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.49+17313G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539338 | |||||||
| chr4:158539370 | T | C | 16 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0195 others(13): Show |
16 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+17345T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539370 | |||||||
| chr4:158539490 | AT | A | 19 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0195 others(16): Show |
19 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.49+17468delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158539490 | ||||||
| chr4:158539570 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+17545G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539570 | |||||||
| chr4:158539654 | G | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+17629G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539654 | |||||||
| chr4:158539656 | G | A | 13 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0195 others(10): Show |
13 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.49+17631G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539656 | |||||||
| chr4:158539813 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+17788A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539813 | |||||||
| chr4:158539814 | A | G | 8 | a0001c0001t0001g0161 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG01123.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+17789A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539814 | |||||||
| chr4:158539974 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.49+17949T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158539974 | |||||||
| chr4:158540086 | G | A | 8 | a0001c0001t0001g0161 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG01123.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+18061G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540086 | |||||||
| chr4:158540128 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+18103G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540128 | |||||||
| chr4:158540147 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.49+18122A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540147 | |||||||
| chr4:158540158 | GTGAAAGC | G | 3 | a0003c0003t0001g0005 a0003c0003t0001g0006 a0006c0005t0002g0207 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49+18134_49+18140d others(9): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540158 | |||||||
| chr4:158540207 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.49+18182G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540207 | |||||||
| chr4:158540355 | G | A | 3 | a0003c0003t0001g0005 a0003c0003t0001g0006 a0006c0005t0002g0207 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49+18330G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540355 | |||||||
| chr4:158540648 | A | G | 1 | a0006c0005t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.49+18623A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540648 | |||||||
| chr4:158540724 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.49+18699G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540724 | |||||||
| chr4:158540755 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.49+18730C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540755 | |||||||
| chr4:158540756 | C | T | 17 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(14): Show |
17 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.49+18731C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540756 | |||||||
| chr4:158540802 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.49+18777A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540802 | |||||||
| chr4:158540825 | C | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.49+18800C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540825 | |||||||
| chr4:158540905 | C | G | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.49+18880C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540905 | |||||||
| chr4:158540948 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+18923T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540948 | |||||||
| chr4:158540976 | G | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.49+18951G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158540976 | |||||||
| chr4:158541143 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.49+19118G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158541143 | |||||||
| chr4:158541350 | G | GCA | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+19356_49+19357d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACA | 2 | a0001c0001t0001g0190 a0001c0001t0002g0109 |
2 | HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.49+19354_49+19357d others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACA | 9 | a0001c0001t0001g0105 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01981.hp2 HG02148.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+19352_49+19357d others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACAC others(1): Show |
28 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0068 others(25): Show |
28 | HG01081.hp1 HG01099.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.49+19350_49+19357d others(10): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACAC others(3): Show |
85 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.49+19348_49+19357d others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACAC others(5): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0016 others(23): Show |
27 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+19346_49+19357d others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACAC others(7): Show |
22 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
22 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.49+19344_49+19357d others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACAC others(9): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0087 |
2 | HG01071.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.49+19342_49+19357d others(18): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACAC others(11): Show |
5 | a0001c0001t0001g0032 a0001c0001t0001g0164 a0001c0001t0002g0115 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+19340_49+19357d others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACAC others(13): Show |
5 | a0001c0001t0001g0160 a0001c0001t0001g0168 a0001c0001t0001g0198 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+19338_49+19357d others(22): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541350 | G | GCACACAC others(15): Show |
4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0003c0003t0001g0005 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+19336_49+19357d others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541350 | ||||||
| chr4:158541380 | A | ACACACAC others(3): Show |
2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01123.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.49+19357_49+19358i others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158541380 | ||||||
| chr4:158542079 | C | CCATATAT others(3): Show |
2 | a0001c0001t0001g0008 a0001c0001t0002g0109 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.49+20054_49+20055i others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542079 | |||||||
| chr4:158542079 | C | CCATATAT others(5): Show |
3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG01891.hp1 HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.49+20054_49+20055i others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542079 | |||||||
| chr4:158542079 | C | CCATATAT others(7): Show |
6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0166 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+20054_49+20055i others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542079 | |||||||
| chr4:158542079 | C | CCATATAT others(9): Show |
1 | a0001c0001t0001g0009 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.49+20054_49+20055i others(18): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542079 | |||||||
| chr4:158542079 | C | CCATATAT others(11): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG01433.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.49+20054_49+20055i others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542079 | |||||||
| chr4:158542079 | C | CCATATAT others(15): Show |
1 | a0001c0001t0001g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.49+20054_49+20055i others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542079 | |||||||
| chr4:158542079 | CTA | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0117 others(12): Show |
16 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+20084_49+20085d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542079 | ||||||
| chr4:158542079 | CTATATA | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0194 |
2 | HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.49+20080_49+20085d others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542079 | ||||||
| chr4:158542079 | CTATATAT others(1): Show |
C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0025 others(1): Show |
4 | HG00558.hp1 HG00735.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+20078_49+20085d others(10): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542079 | ||||||
| chr4:158542079 | CTATATAT others(3): Show |
C | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.49+20076_49+20085d others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542079 | ||||||
| chr4:158542080 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(101): Show |
106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.49+20055T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542080 | |||||||
| chr4:158542083 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.49+20058A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542083 | |||||||
| chr4:158542084 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.49+20059T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542084 | |||||||
| chr4:158542086 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0194 |
2 | HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.49+20061T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542086 | |||||||
| chr4:158542088 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0025 others(1): Show |
4 | HG00558.hp1 HG00735.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+20063T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542088 | |||||||
| chr4:158542090 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.49+20065T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542090 | |||||||
| chr4:158542090 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.49+20066_49+20078d others(15): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542090 | |||||||
| chr4:158542098 | TATATATA | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0184 a0001c0001t0001g0191 |
4 | HG03491.hp2 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+20074_49+20080d others(9): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542098 | |||||||
| chr4:158542101 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+20078_49+20089d others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542101 | ||||||
| chr4:158542105 | A | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG00558.hp1 HG00735.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+20080A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542105 | |||||||
| chr4:158542107 | A | ATTTT | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0157 others(1): Show |
4 | HG02922.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+20083_49+20084i others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542107 | ||||||
| chr4:158542107 | A | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(13): Show |
17 | HG00558.hp1 HG00735.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.49+20082A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542107 | |||||||
| chr4:158542109 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0090 |
2 | HG00733.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(19): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(29): Show |
1 | a0001c0001t0005g0052 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(38): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0047 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(33): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(35): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(36): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(28): Show |
1 | a0002c0002t0001g0101 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(37): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(25): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0138 |
2 | HG02523.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(34): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(27): Show |
2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(36): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0140 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(32): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0121 |
2 | HG02698.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(28): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(32): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0105 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0192 |
2 | NA18947.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(26): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0096 a0001c0001t0001g0122 a0001c0001t0001g0139 |
3 | HG02886.hp2 HG03239.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(28): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0021 a0001c0001t0001g0107 |
2 | HG01358.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(23): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0159 |
2 | HG02647.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(25): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(17): Show |
9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0086 others(6): Show |
9 | HG00140.hp1 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+20085_49+20086i others(26): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(29): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0190 |
2 | HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(22): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0182 |
2 | HG00738.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(23): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(15): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0133 others(2): Show |
5 | HG01071.hp1 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+20085_49+20086i others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(28): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(21): Show |
1 | a0001c0001t0002g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(30): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0070 |
2 | HG01074.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(19): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0064 |
2 | NA18951.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(13): Show |
13 | a0001c0001t0001g0016 a0001c0001t0001g0069 a0001c0001t0001g0099 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.49+20085_49+20086i others(22): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0128 |
2 | HG03486.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(23): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(27): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(28): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(18): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(11): Show |
6 | a0001c0001t0001g0054 a0001c0001t0001g0068 a0001c0001t0001g0126 others(3): Show |
6 | HG00438.hp1 HG01081.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+20085_49+20086i others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(15): Show |
1 | a0001c0001t0004g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0197 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(15): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(7): Show |
11 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0051 others(8): Show |
11 | HG01081.hp2 HG02523.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+20085_49+20086i others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(17): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0186 |
3 | HG00099.hp1 HG01168.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(18): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(13): Show |
1 | a0001c0001t0004g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(22): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(5): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0044 others(14): Show |
18 | HG00438.hp2 HG00558.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.49+20085_49+20086i others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.49+20085_49+20086i others(15): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(7): Show |
8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0056 others(5): Show |
8 | HG00140.hp2 HG01943.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+20085_49+20086i others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(17): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0046 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(13): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATAT others(5): Show |
8 | a0001c0001t0001g0050 a0001c0001t0001g0095 a0001c0001t0001g0098 others(5): Show |
8 | HG00280.hp2 HG01071.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+20085_49+20086i others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542109 | ||||||
| chr4:158542109 | A | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(35): Show |
40 | HG00558.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.49+20084A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542109 | |||||||
| chr4:158542110 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.49+20085_49+20086i others(25): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542110 | |||||||
| chr4:158542110 | T | TATATATA others(18): Show |
1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.49+20085_49+20086i others(27): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542110 | |||||||
| chr4:158542111 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+20086T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542111 | |||||||
| chr4:158542112 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.49+20087T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542112 | |||||||
| chr4:158542113 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+20088T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542113 | |||||||
| chr4:158542421 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.49+20396A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542421 | |||||||
| chr4:158542453 | C | G | 1 | a0006c0005t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.49+20428C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542453 | |||||||
| chr4:158542677 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.49+20652C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542677 | |||||||
| chr4:158542678 | G | A | 12 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
12 | HG02129.hp1 HG02723.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+20653G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542678 | |||||||
| chr4:158542743 | A | T | 3 | a0003c0003t0001g0005 a0003c0003t0001g0006 a0006c0005t0002g0207 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49+20718A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542743 | |||||||
| chr4:158542788 | AT | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.49+20765delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542788 | ||||||
| chr4:158542794 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.49+20769A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542794 | |||||||
| chr4:158542840 | C | CA | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.49+20817dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158542840 | ||||||
| chr4:158542843 | C | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.49+20818C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542843 | |||||||
| chr4:158542971 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.49+20946G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542971 | |||||||
| chr4:158543130 | C | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.49+21105C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543130 | |||||||
| chr4:158543153 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.49+21128G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543153 | |||||||
| chr4:158543188 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+21163C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543188 | |||||||
| chr4:158543519 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49+21494A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543519 | |||||||
| chr4:158543580 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.49+21555A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543580 | |||||||
| chr4:158543628 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 others(1): Show |
4 | HG02109.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+21603C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543628 | |||||||
| chr4:158543669 | CCATTT | C | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+21648_49+21652d others(7): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158543669 | ||||||
| chr4:158543737 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.49+21712A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543737 | |||||||
| chr4:158543747 | C | CT | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+21728dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158543747 | ||||||
| chr4:158543818 | C | T | 3 | a0003c0003t0001g0005 a0003c0003t0001g0006 a0006c0005t0002g0207 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49+21793C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543818 | |||||||
| chr4:158543843 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.49+21818A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543843 | |||||||
| chr4:158543927 | T | C | 1 | a0001c0001t0001g0011 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.49+21902T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543927 | |||||||
| chr4:158543974 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+21949G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543974 | |||||||
| chr4:158543984 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+21959G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158543984 | |||||||
| chr4:158544001 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02723.hp1 HG03516.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+21976C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544001 | |||||||
| chr4:158544036 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.49+22011G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544036 | |||||||
| chr4:158544213 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.49+22188C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544213 | |||||||
| chr4:158544260 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+22235G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544260 | |||||||
| chr4:158544377 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.49+22352T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544377 | |||||||
| chr4:158544416 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+22391A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544416 | |||||||
| chr4:158544436 | CT | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.49+22422delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158544436 | ||||||
| chr4:158544455 | T | A | 3 | a0003c0003t0001g0005 a0003c0003t0001g0006 a0006c0005t0002g0207 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49+22430T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544455 | |||||||
| chr4:158544486 | A | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+22461A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544486 | |||||||
| chr4:158544555 | T | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.49+22530T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544555 | |||||||
| chr4:158544596 | C | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+22571C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544596 | |||||||
| chr4:158544599 | A | C | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+22574A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544599 | |||||||
| chr4:158544717 | A | G | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+22692A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544717 | |||||||
| chr4:158544954 | T | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.49+22929T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544954 | |||||||
| chr4:158544956 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.49+22931T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544956 | |||||||
| chr4:158544975 | G | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+22950G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158544975 | |||||||
| chr4:158545096 | C | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01123.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.49+23071C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158545096 | |||||||
| chr4:158545161 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49+23136C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158545161 | |||||||
| chr4:158545276 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+23251G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158545276 | |||||||
| chr4:158545616 | T | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.49+23591T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158545616 | |||||||
| chr4:158545945 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49+23920T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158545945 | |||||||
| chr4:158545966 | G | GT | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+23947dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158545966 | ||||||
| chr4:158546025 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(65): Show |
69 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.49+24000A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546025 | |||||||
| chr4:158546204 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.49+24179T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546204 | |||||||
| chr4:158546601 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.49+24576T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546601 | |||||||
| chr4:158546635 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.49+24610A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546635 | |||||||
| chr4:158546648 | T | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.49+24623T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546648 | |||||||
| chr4:158546662 | G | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0110 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+24637G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546662 | |||||||
| chr4:158546663 | G | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+24638G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546663 | |||||||
| chr4:158546699 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+24674T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546699 | |||||||
| chr4:158546743 | G | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.49+24718G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546743 | |||||||
| chr4:158546769 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.49+24744T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546769 | |||||||
| chr4:158546793 | T | A | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.49+24768T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546793 | |||||||
| chr4:158546809 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.49+24784A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546809 | |||||||
| chr4:158546879 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+24854A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546879 | |||||||
| chr4:158546881 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49+24856G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546881 | |||||||
| chr4:158546975 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.49+24950G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546975 | |||||||
| chr4:158546981 | A | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+24956A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158546981 | |||||||
| chr4:158547177 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+25152G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547177 | |||||||
| chr4:158547539 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-25159G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547539 | |||||||
| chr4:158547624 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(65): Show |
69 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.50-25074C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547624 | |||||||
| chr4:158547625 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(65): Show |
69 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.50-25073A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547625 | |||||||
| chr4:158547700 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-24998A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547700 | |||||||
| chr4:158547778 | C | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.50-24920C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547778 | |||||||
| chr4:158547797 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(108): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.50-24901G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547797 | |||||||
| chr4:158547797 | G | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0157 a0001c0001t0001g0193 |
3 | HG03098.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-24901G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547797 | |||||||
| chr4:158547890 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.50-24808T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547890 | |||||||
| chr4:158547893 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.50-24805C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158547893 | |||||||
| chr4:158548022 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.50-24676G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548022 | |||||||
| chr4:158548090 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0157 a0001c0001t0001g0193 |
3 | HG03098.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-24608T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548090 | |||||||
| chr4:158548148 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.50-24550C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548148 | |||||||
| chr4:158548158 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.50-24540G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548158 | |||||||
| chr4:158548173 | A | C | 2 | a0001c0001t0001g0104 a0001c0001t0002g0181 |
2 | NA18977.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.50-24525A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548173 | |||||||
| chr4:158548287 | G | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.50-24411G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548287 | |||||||
| chr4:158548382 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.50-24316G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548382 | |||||||
| chr4:158548441 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.50-24257C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548441 | |||||||
| chr4:158548611 | G | T | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-24087G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548611 | |||||||
| chr4:158548695 | A | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02129.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.50-24003A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548695 | |||||||
| chr4:158548706 | T | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02129.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.50-23992T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548706 | |||||||
| chr4:158548810 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.50-23888C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548810 | |||||||
| chr4:158548811 | G | A | 12 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
12 | HG02129.hp1 HG02723.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-23887G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548811 | |||||||
| chr4:158548839 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.50-23859T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548839 | |||||||
| chr4:158548886 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-23812T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548886 | |||||||
| chr4:158548964 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(61): Show |
65 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.50-23734G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548964 | |||||||
| chr4:158549096 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(62): Show |
66 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.50-23602C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549096 | |||||||
| chr4:158549135 | A | G | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-23563A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549135 | |||||||
| chr4:158549145 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.50-23553C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549145 | |||||||
| chr4:158549146 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01099.hp1 HG01255.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.50-23552G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549146 | |||||||
| chr4:158549198 | A | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.50-23500A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549198 | |||||||
| chr4:158549238 | C | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.50-23460C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549238 | |||||||
| chr4:158549239 | G | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-23459G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549239 | |||||||
| chr4:158549243 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-23455C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549243 | |||||||
| chr4:158549279 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-23419C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549279 | |||||||
| chr4:158549396 | A | G | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-23302A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549396 | |||||||
| chr4:158549466 | C | T | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.50-23232C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549466 | |||||||
| chr4:158549483 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0005g0039 |
2 | NA19007.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.50-23215G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549483 | |||||||
| chr4:158549489 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.50-23209A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549489 | |||||||
| chr4:158549524 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.50-23174G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549524 | |||||||
| chr4:158549863 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-22835G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549863 | |||||||
| chr4:158549925 | C | T | 3 | a0003c0003t0001g0005 a0003c0003t0001g0006 a0006c0005t0002g0207 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.50-22773C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158549925 | |||||||
| chr4:158550049 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.50-22649G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158550049 | |||||||
| chr4:158550101 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-22597C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158550101 | |||||||
| chr4:158550131 | C | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.50-22567C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158550131 | |||||||
| chr4:158550272 | T | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.50-22426T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158550272 | |||||||
| chr4:158550418 | G | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-22280G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158550418 | |||||||
| chr4:158550451 | C | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.50-22247C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158550451 | |||||||
| chr4:158550805 | C | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-21893C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158550805 | |||||||
| chr4:158550984 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.50-21714A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158550984 | |||||||
| chr4:158551063 | T | TGTTTTGG others(21): Show |
4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-21635_50-21634i others(30): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551063 | |||||||
| chr4:158551065 | A | T | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-21633A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551065 | |||||||
| chr4:158551071 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-21627C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551071 | |||||||
| chr4:158551151 | T | C | 4 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-21547T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551151 | |||||||
| chr4:158551290 | T | A | 12 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
12 | HG02129.hp1 HG02723.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-21408T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551290 | |||||||
| chr4:158551303 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.50-21395G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551303 | |||||||
| chr4:158551354 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.50-21344A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551354 | |||||||
| chr4:158551538 | GATT | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(62): Show |
66 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.50-21157_50-21155d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158551538 | ||||||
| chr4:158551666 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-21032C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551666 | |||||||
| chr4:158551706 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.50-20992C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551706 | |||||||
| chr4:158551802 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.50-20896A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551802 | |||||||
| chr4:158551854 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-20844T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551854 | |||||||
| chr4:158551919 | G | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-20779G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551919 | |||||||
| chr4:158551933 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.50-20765C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551933 | |||||||
| chr4:158552131 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.50-20567G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158552131 | |||||||
| chr4:158552171 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.50-20527C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158552171 | |||||||
| chr4:158552267 | T | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02129.hp1 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.50-20431T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158552267 | |||||||
| chr4:158552417 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-20281G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158552417 | |||||||
| chr4:158552558 | T | A | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.50-20140T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158552558 | |||||||
| chr4:158552761 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-19937A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158552761 | |||||||
| chr4:158553043 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-19655G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158553043 | |||||||
| chr4:158553044 | C | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-19654C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158553044 | |||||||
| chr4:158553167 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.50-19531C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158553167 | |||||||
| chr4:158553480 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.50-19218C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158553480 | |||||||
| chr4:158553502 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.50-19196C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158553502 | |||||||
| chr4:158553633 | G | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-19065G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158553633 | |||||||
| chr4:158554237 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0092 |
2 | HG00438.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.50-18461C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158554237 | |||||||
| chr4:158554272 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.50-18426G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158554272 | |||||||
| chr4:158554279 | T | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0066 |
2 | NA18951.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.50-18419T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158554279 | |||||||
| chr4:158554290 | T | C | 4 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-18408T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158554290 | |||||||
| chr4:158554552 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.50-18146G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158554552 | |||||||
| chr4:158554619 | C | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-18079C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158554619 | |||||||
| chr4:158554768 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.50-17930C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158554768 | |||||||
| chr4:158554988 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-17710T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158554988 | |||||||
| chr4:158555231 | G | A | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG00099.hp2 HG00280.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-17467G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158555231 | |||||||
| chr4:158555302 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.50-17396A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158555302 | |||||||
| chr4:158555357 | A | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.50-17341A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158555357 | |||||||
| chr4:158555419 | A | G | 60 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.50-17279A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158555419 | |||||||
| chr4:158555478 | T | G | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.50-17220T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158555478 | |||||||
| chr4:158555821 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.50-16877C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158555821 | |||||||
| chr4:158556005 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-16693A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158556005 | |||||||
| chr4:158556224 | CA | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.50-16457delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158556224 | ||||||
| chr4:158556312 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-16386G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158556312 | |||||||
| chr4:158556711 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-15987A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158556711 | |||||||
| chr4:158556924 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.50-15774C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158556924 | |||||||
| chr4:158557247 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(13): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-15451G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158557247 | |||||||
| chr4:158557825 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.50-14873G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158557825 | |||||||
| chr4:158558579 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.50-14119G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158558579 | |||||||
| chr4:158558917 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.50-13781A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158558917 | |||||||
| chr4:158559506 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-13192C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158559506 | |||||||
| chr4:158559546 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.50-13152C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158559546 | |||||||
| chr4:158559722 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG00733.hp2 HG01071.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.50-12976C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158559722 | |||||||
| chr4:158559753 | C | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-12945C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158559753 | |||||||
| chr4:158560184 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.50-12514C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560184 | |||||||
| chr4:158560309 | G | T | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-12389G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560309 | |||||||
| chr4:158560338 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.50-12360C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560338 | |||||||
| chr4:158560371 | T | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.50-12327T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560371 | |||||||
| chr4:158560538 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-12160T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560538 | |||||||
| chr4:158560568 | T | C | 1 | a0001c0001t0004g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.50-12130T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560568 | |||||||
| chr4:158560683 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | HG00140.hp2 HG00558.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-12015G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560683 | |||||||
| chr4:158560847 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.50-11851G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560847 | |||||||
| chr4:158561045 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-11653G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158561045 | |||||||
| chr4:158561127 | C | T | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.50-11571C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158561127 | |||||||
| chr4:158561430 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.50-11268A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158561430 | |||||||
| chr4:158561626 | C | CT | 65 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0029 others(62): Show |
65 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.50-11053dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158561626 | ||||||
| chr4:158561626 | C | CTT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0097 others(2): Show |
6 | NA18951.hp1 NA18977.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-11054_50-11053d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158561626 | ||||||
| chr4:158561626 | CT | C | 36 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0016 others(33): Show |
37 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.50-11053delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158561626 | ||||||
| chr4:158561630 | T | C | 1 | a0001c0001t0003g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.50-11068T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158561630 | |||||||
| chr4:158561631 | T | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.50-11067T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158561631 | |||||||
| chr4:158562054 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.50-10644C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158562054 | |||||||
| chr4:158562249 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.50-10449T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158562249 | |||||||
| chr4:158562252 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.50-10446A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158562252 | |||||||
| chr4:158562268 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.50-10430C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158562268 | |||||||
| chr4:158562523 | C | CA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0032 others(42): Show |
45 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.50-10147dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0040 others(21): Show |
25 | HG00642.hp2 HG01123.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-10148_50-10147d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAAAAAA | 16 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0028 others(13): Show |
16 | HG00140.hp2 HG00558.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.50-10152_50-10147d others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAAAAAAA | 43 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0041 others(40): Show |
43 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.50-10153_50-10147d others(9): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAAAAAAA others(1): Show |
11 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0055 others(8): Show |
11 | HG00099.hp1 HG00438.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-10154_50-10147d others(10): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAAAAAAA others(2): Show |
14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(11): Show |
15 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.50-10155_50-10147d others(11): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0155 others(3): Show |
6 | HG00280.hp2 HG01071.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-10156_50-10147d others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0001g0202 others(2): Show |
5 | HG00733.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-10157_50-10147d others(13): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0084 a0001c0001t0001g0201 a0001c0001t0005g0039 |
3 | HG01891.hp2 HG03209.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.50-10158_50-10147d others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0004g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.50-10169_50-10147d others(25): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562523 | CA | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-10147delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562523 | ||||||
| chr4:158562552 | T | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0196 |
2 | HG02145.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.50-10146T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158562552 | |||||||
| chr4:158562693 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-10005C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158562693 | |||||||
| chr4:158562838 | CCAA | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-9856_50-9854del others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158562838 | ||||||
| chr4:158563412 | G | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-9286G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563412 | |||||||
| chr4:158563447 | A | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-9251A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563447 | |||||||
| chr4:158563496 | GCA | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG02129.hp1 HG02258.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.50-9162_50-9161del others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158563496 | ||||||
| chr4:158563496 | GCACA | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0027 others(74): Show |
79 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.50-9164_50-9161del others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158563496 | ||||||
| chr4:158563496 | GCACACA | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.50-9166_50-9161del others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158563496 | ||||||
| chr4:158563496 | GCACACAC others(1): Show |
G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0182 a0001c0001t0001g0193 others(3): Show |
6 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-9168_50-9161del others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158563496 | ||||||
| chr4:158563496 | GCACACAC others(3): Show |
G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | HG01074.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.50-9170_50-9161del others(10): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158563496 | ||||||
| chr4:158563536 | A | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0134 |
2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.50-9162A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563536 | |||||||
| chr4:158563570 | C | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02615.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.50-9128C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563570 | |||||||
| chr4:158563572 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.50-9126C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563572 | |||||||
| chr4:158563590 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.50-9108A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563590 | |||||||
| chr4:158563677 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.50-9021C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563677 | |||||||
| chr4:158563802 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.50-8896C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563802 | |||||||
| chr4:158563819 | T | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-8879T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563819 | |||||||
| chr4:158563899 | C | A | 4 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-8799C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158563899 | |||||||
| chr4:158564057 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.50-8641T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158564057 | |||||||
| chr4:158564520 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-8178G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158564520 | |||||||
| chr4:158564682 | AGATGGAT others(4): Show |
A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-8014_50-8004del others(11): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158564682 | ||||||
| chr4:158564866 | C | T | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-7832C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158564866 | |||||||
| chr4:158564870 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-7828T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158564870 | |||||||
| chr4:158564935 | T | C | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.50-7763T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158564935 | |||||||
| chr4:158565094 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.50-7604G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158565094 | |||||||
| chr4:158565191 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.50-7507A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158565191 | |||||||
| chr4:158565329 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.50-7369G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158565329 | |||||||
| chr4:158565645 | A | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.50-7053A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158565645 | |||||||
| chr4:158565693 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.50-7005C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158565693 | |||||||
| chr4:158565816 | C | G | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.50-6882C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158565816 | |||||||
| chr4:158566077 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0090 |
2 | HG00733.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.50-6621C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566077 | |||||||
| chr4:158566375 | T | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02615.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.50-6323T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566375 | |||||||
| chr4:158566387 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0066 |
2 | NA18951.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.50-6311G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566387 | |||||||
| chr4:158566387 | G | GAC | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.50-6310_50-6309ins others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158566387 | ||||||
| chr4:158566394 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-6304G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566394 | |||||||
| chr4:158566646 | A | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02615.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.50-6052A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566646 | |||||||
| chr4:158566657 | C | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.50-6041C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566657 | |||||||
| chr4:158566706 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.50-5992C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566706 | |||||||
| chr4:158566822 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50-5876G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566822 | |||||||
| chr4:158566842 | C | T | 51 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(48): Show |
51 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.50-5856C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566842 | |||||||
| chr4:158566973 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0002g0109 a0003c0003t0001g0005 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-5725G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158566973 | |||||||
| chr4:158567003 | G | A | 4 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-5695G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567003 | |||||||
| chr4:158567133 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.50-5565C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567133 | |||||||
| chr4:158567210 | G | A | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.50-5488G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567210 | |||||||
| chr4:158567239 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.50-5459C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567239 | |||||||
| chr4:158567318 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.50-5380C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567318 | |||||||
| chr4:158567334 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-5364C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567334 | |||||||
| chr4:158567686 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0112 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.50-5012A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567686 | |||||||
| chr4:158567729 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.50-4969T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567729 | |||||||
| chr4:158567850 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.50-4848T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567850 | |||||||
| chr4:158567884 | C | A | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.50-4814C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567884 | |||||||
| chr4:158567913 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.50-4785C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567913 | |||||||
| chr4:158567933 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.50-4765C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567933 | |||||||
| chr4:158567995 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.50-4703C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158567995 | |||||||
| chr4:158568000 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.50-4698A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568000 | |||||||
| chr4:158568028 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0187 |
2 | HG00280.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.50-4670T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568028 | |||||||
| chr4:158568038 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.50-4660G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568038 | |||||||
| chr4:158568043 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.50-4655C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568043 | |||||||
| chr4:158568054 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.50-4644A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568054 | |||||||
| chr4:158568065 | C | T | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.50-4633C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568065 | |||||||
| chr4:158568072 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.50-4626A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568072 | |||||||
| chr4:158568201 | T | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-4497T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568201 | |||||||
| chr4:158568203 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.50-4495C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568203 | |||||||
| chr4:158568266 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0092 |
2 | HG00438.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.50-4432G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568266 | |||||||
| chr4:158568280 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-4418C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568280 | |||||||
| chr4:158568290 | A | G | 1 | a0004c0006t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.50-4408A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568290 | |||||||
| chr4:158568347 | A | G | 4 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-4351A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568347 | |||||||
| chr4:158568413 | G | C | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-4285G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568413 | |||||||
| chr4:158568451 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-4247T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568451 | |||||||
| chr4:158568454 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.50-4244A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568454 | |||||||
| chr4:158568565 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.50-4133T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568565 | |||||||
| chr4:158568583 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.50-4115G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568583 | |||||||
| chr4:158568706 | C | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.50-3992C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568706 | |||||||
| chr4:158568752 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.50-3946G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568752 | |||||||
| chr4:158568992 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.50-3706G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158568992 | |||||||
| chr4:158569150 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.50-3548C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158569150 | |||||||
| chr4:158569217 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.50-3481G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158569217 | |||||||
| chr4:158569282 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.50-3416A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158569282 | |||||||
| chr4:158569631 | G | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.50-3067G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158569631 | |||||||
| chr4:158569858 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.50-2840C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158569858 | |||||||
| chr4:158569931 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.50-2767A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158569931 | |||||||
| chr4:158569991 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.50-2707G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158569991 | |||||||
| chr4:158570088 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.50-2610G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158570088 | |||||||
| chr4:158570180 | TAA | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0017 others(14): Show |
18 | HG00558.hp1 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.50-2516_50-2515del others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158570180 | ||||||
| chr4:158570525 | A | C | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-2173A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158570525 | |||||||
| chr4:158570772 | T | C | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1926T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158570772 | |||||||
| chr4:158570806 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.50-1892C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158570806 | |||||||
| chr4:158570873 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0097 others(1): Show |
5 | NA18951.hp1 NA19004.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-1825C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158570873 | |||||||
| chr4:158570909 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.50-1789G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158570909 | |||||||
| chr4:158571043 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.50-1655C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571043 | |||||||
| chr4:158571238 | C | T | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-1460C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571238 | |||||||
| chr4:158571469 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.50-1229C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571469 | |||||||
| chr4:158571527 | T | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(70): Show |
74 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.50-1171T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571527 | |||||||
| chr4:158571620 | C | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1078C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571620 | |||||||
| chr4:158571622 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.50-1076G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571622 | |||||||
| chr4:158571639 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.50-1059G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571639 | |||||||
| chr4:158571760 | G | GA | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.50-936dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 158571760 | ||||||
| chr4:158571946 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.50-752G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571946 | |||||||
| chr4:158572013 | T | A | 1 | a0001c0001t0001g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.50-685T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158572013 | |||||||
| chr4:158572085 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.50-613C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158572085 | |||||||
| chr4:158572550 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-148G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158572550 | |||||||
| chr4:158572904 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.187+69C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158572904 | |||||||
| chr4:158573018 | G | GT | 95 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.187+192dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158573018 | ||||||
| chr4:158573041 | G | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+206G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158573041 | |||||||
| chr4:158573077 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | NA19004.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.187+242C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158573077 | |||||||
| chr4:158573103 | G | A | 1 | a0006c0005t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+268G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158573103 | |||||||
| chr4:158573244 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.187+409G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158573244 | |||||||
| chr4:158573367 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.187+532T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158573367 | |||||||
| chr4:158573406 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(9): Show |
13 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+571G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158573406 | |||||||
| chr4:158573428 | C | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.187+593C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158573428 | |||||||
| chr4:158574234 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.187+1399G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158574234 | |||||||
| chr4:158574571 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.187+1736C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158574571 | |||||||
| chr4:158574642 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.187+1807C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158574642 | |||||||
| chr4:158574891 | T | TA | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.187+2064dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158574891 | ||||||
| chr4:158574904 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
114 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.187+2069G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158574904 | |||||||
| chr4:158574995 | G | A | 3 | a0002c0002t0001g0101 a0002c0002t0001g0102 a0002c0002t0001g0103 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.187+2160G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158574995 | |||||||
| chr4:158575419 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.187+2584G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158575419 | |||||||
| chr4:158575464 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.187+2629C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158575464 | |||||||
| chr4:158575554 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0017 others(13): Show |
17 | HG00558.hp1 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+2719G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158575554 | |||||||
| chr4:158575942 | C | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.187+3107C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158575942 | |||||||
| chr4:158576178 | A | G | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG00099.hp2 HG00280.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+3343A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576178 | |||||||
| chr4:158576319 | G | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.187+3484G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576319 | |||||||
| chr4:158576405 | A | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.187+3570A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576405 | |||||||
| chr4:158576525 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.187+3690G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576525 | |||||||
| chr4:158576628 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.187+3793A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576628 | |||||||
| chr4:158576641 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.187+3806A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576641 | |||||||
| chr4:158576727 | TGCTAGTA others(3): Show |
T | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.187+3895_187+3904d others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158576727 | ||||||
| chr4:158576774 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.187+3939G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576774 | |||||||
| chr4:158576792 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.187+3957G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576792 | |||||||
| chr4:158576801 | G | T | 2 | a0001c0001t0001g0107 a0001c0001t0005g0039 |
2 | NA19007.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.187+3966G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158576801 | |||||||
| chr4:158577012 | TTTC | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(120): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.187+4204_187+4206d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158577012 | ||||||
| chr4:158577012 | TTTCTTC | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG01123.hp1 HG02145.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+4201_187+4206d others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158577012 | ||||||
| chr4:158577371 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.187+4536T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158577371 | |||||||
| chr4:158577387 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.187+4552T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158577387 | |||||||
| chr4:158577445 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.187+4610G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158577445 | |||||||
| chr4:158577642 | A | G | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+4807A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158577642 | |||||||
| chr4:158578078 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0065 |
2 | HG01074.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.187+5243T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158578078 | |||||||
| chr4:158578223 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.187+5388T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158578223 | |||||||
| chr4:158578224 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.187+5389C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158578224 | |||||||
| chr4:158578509 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.187+5674C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158578509 | |||||||
| chr4:158578837 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.187+6002T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158578837 | |||||||
| chr4:158579209 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
98 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.187+6374A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579209 | |||||||
| chr4:158579332 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
98 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.187+6497A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579332 | |||||||
| chr4:158579436 | T | G | 1 | a0001c0001t0001g0058 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.187+6601T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579436 | |||||||
| chr4:158579475 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0176 |
2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.187+6640A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579475 | |||||||
| chr4:158579507 | G | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.187+6672G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579507 | |||||||
| chr4:158579668 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.187+6833G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579668 | |||||||
| chr4:158579814 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
98 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.187+6979T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579814 | |||||||
| chr4:158579907 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.187+7072G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579907 | |||||||
| chr4:158579926 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.187+7091A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579926 | |||||||
| chr4:158580140 | C | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.187+7305C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158580140 | |||||||
| chr4:158580165 | C | G | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.187+7330C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158580165 | |||||||
| chr4:158580278 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.187+7443G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158580278 | |||||||
| chr4:158580511 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.187+7676G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158580511 | |||||||
| chr4:158580915 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.187+8080A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158580915 | |||||||
| chr4:158581084 | C | T | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.187+8249C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158581084 | |||||||
| chr4:158581606 | G | T | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.187+8771G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158581606 | |||||||
| chr4:158581787 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.187+8952T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158581787 | |||||||
| chr4:158581883 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.187+9048A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158581883 | |||||||
| chr4:158581949 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.187+9114A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158581949 | |||||||
| chr4:158582317 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0121 |
2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.187+9482C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158582317 | |||||||
| chr4:158582355 | G | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.187+9520G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158582355 | |||||||
| chr4:158582459 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
114 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.187+9624C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158582459 | |||||||
| chr4:158582622 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(73): Show |
77 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.187+9787A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158582622 | |||||||
| chr4:158582945 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.187+10110A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158582945 | |||||||
| chr4:158583095 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.187+10260G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158583095 | |||||||
| chr4:158583317 | A | C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.188-10084A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158583317 | |||||||
| chr4:158583821 | A | G | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.188-9580A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158583821 | |||||||
| chr4:158583868 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.188-9533A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158583868 | |||||||
| chr4:158584009 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0192 |
2 | HG02523.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.188-9392G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158584009 | |||||||
| chr4:158584274 | G | C | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(4): Show |
7 | HG00140.hp1 HG01261.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-9127G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158584274 | |||||||
| chr4:158584381 | C | T | 16 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 others(13): Show |
16 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.188-9020C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158584381 | |||||||
| chr4:158584861 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.188-8540C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158584861 | |||||||
| chr4:158585474 | G | T | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.188-7927G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158585474 | |||||||
| chr4:158585687 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.188-7714G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158585687 | |||||||
| chr4:158585708 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.188-7693A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158585708 | |||||||
| chr4:158585886 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188-7515T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158585886 | |||||||
| chr4:158586068 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.188-7333C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158586068 | |||||||
| chr4:158586203 | C | A | 7 | a0001c0001t0001g0108 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-7198C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158586203 | |||||||
| chr4:158586452 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.188-6949C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158586452 | |||||||
| chr4:158586490 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00733.hp2 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-6911C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158586490 | |||||||
| chr4:158586749 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.188-6652G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158586749 | |||||||
| chr4:158587149 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.188-6252T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158587149 | |||||||
| chr4:158587287 | C | T | 2 | a0001c0001t0002g0109 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.188-6114C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158587287 | |||||||
| chr4:158587560 | C | T | 1 | a0006c0005t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.188-5841C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158587560 | |||||||
| chr4:158587704 | TAGTC | T | 5 | a0001c0001t0001g0091 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG01884.hp2 HG01943.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-5694_188-5691d others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158587704 | ||||||
| chr4:158587781 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(18): Show |
22 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.188-5620T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158587781 | |||||||
| chr4:158588007 | A | C | 6 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG02055.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-5394A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158588007 | |||||||
| chr4:158588035 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(30): Show |
34 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.188-5366G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158588035 | |||||||
| chr4:158588090 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.188-5311G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158588090 | |||||||
| chr4:158588117 | C | T | 14 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0111 others(11): Show |
14 | HG02129.hp1 HG02602.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.188-5284C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158588117 | |||||||
| chr4:158588537 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.188-4864C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158588537 | |||||||
| chr4:158588543 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.188-4858G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158588543 | |||||||
| chr4:158589003 | A | G | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-4398A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158589003 | |||||||
| chr4:158589066 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.188-4335C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158589066 | |||||||
| chr4:158589159 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.188-4242A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158589159 | |||||||
| chr4:158589178 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0126 others(6): Show |
9 | HG01081.hp1 HG02055.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-4223C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158589178 | |||||||
| chr4:158589491 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-3910A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158589491 | |||||||
| chr4:158589531 | A | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-3870A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158589531 | |||||||
| chr4:158589600 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.188-3801A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158589600 | |||||||
| chr4:158589826 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.188-3575G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158589826 | |||||||
| chr4:158590060 | A | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(93): Show |
98 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.188-3341A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158590060 | |||||||
| chr4:158590102 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.188-3299G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158590102 | |||||||
| chr4:158590120 | G | A | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.188-3281G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158590120 | |||||||
| chr4:158590412 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG00642.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.188-2989G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158590412 | |||||||
| chr4:158590581 | C | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-2820C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158590581 | |||||||
| chr4:158590634 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.188-2767T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158590634 | |||||||
| chr4:158590691 | C | T | 14 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0111 others(11): Show |
14 | HG02129.hp1 HG02602.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.188-2710C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158590691 | |||||||
| chr4:158590778 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.188-2623C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158590778 | |||||||
| chr4:158591051 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.188-2350A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591051 | |||||||
| chr4:158591442 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0095 others(2): Show |
6 | NA18947.hp2 NA18951.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-1959T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591442 | |||||||
| chr4:158591486 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.188-1915G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591486 | |||||||
| chr4:158591501 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-1900C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591501 | |||||||
| chr4:158591508 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.188-1893C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591508 | |||||||
| chr4:158591585 | C | CA | 21 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0050 others(18): Show |
21 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.188-1798dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158591585 | ||||||
| chr4:158591585 | CA | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0159 others(2): Show |
5 | HG00735.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-1798delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158591585 | ||||||
| chr4:158591609 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.188-1792C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591609 | |||||||
| chr4:158591712 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.188-1689G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591712 | |||||||
| chr4:158591740 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0113 others(1): Show |
4 | HG02723.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-1661C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591740 | |||||||
| chr4:158591812 | A | T | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.188-1589A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591812 | |||||||
| chr4:158591853 | T | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.188-1548T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591853 | |||||||
| chr4:158591905 | G | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.188-1496G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591905 | |||||||
| chr4:158591958 | T | A | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.188-1443T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158591958 | |||||||
| chr4:158592159 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.188-1242G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158592159 | |||||||
| chr4:158592166 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.188-1235T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158592166 | |||||||
| chr4:158592442 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-959C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158592442 | |||||||
| chr4:158592464 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.188-937C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158592464 | |||||||
| chr4:158592499 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.188-902A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158592499 | |||||||
| chr4:158592777 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.188-624A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158592777 | |||||||
| chr4:158592816 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.188-585C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158592816 | |||||||
| chr4:158592925 | TA | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.188-463delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158592925 | ||||||
| chr4:158593102 | A | AAAAC | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
113 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.188-291_188-288dup others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158593102 | ||||||
| chr4:158593141 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.188-260T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158593141 | |||||||
| chr4:158593167 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.188-234G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158593167 | |||||||
| chr4:158593256 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.188-145C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158593256 | |||||||
| chr4:158593285 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.188-116A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158593285 | |||||||
| chr4:158593302 | GA | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.188-96delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 158593302 | ||||||
| chr4:158593314 | C | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.188-87C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158593314 | |||||||
| chr4:158593633 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.286+134C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158593633 | |||||||
| chr4:158594044 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.286+545A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158594044 | |||||||
| chr4:158594094 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.286+595G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158594094 | |||||||
| chr4:158594201 | TC | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.286+703delC | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158594201 | |||||||
| chr4:158594228 | G | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
117 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.286+729G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158594228 | |||||||
| chr4:158594501 | C | CT | 32 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(29): Show |
33 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.286+1014dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 158594501 | ||||||
| chr4:158594518 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.286+1019A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158594518 | |||||||
| chr4:158594668 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.286+1169A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158594668 | |||||||
| chr4:158594702 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.286+1203T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158594702 | |||||||
| chr4:158594772 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.286+1273T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158594772 | |||||||
| chr4:158595013 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.286+1514G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158595013 | |||||||
| chr4:158595194 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0075 |
2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.286+1695G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158595194 | |||||||
| chr4:158595280 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.286+1781A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158595280 | |||||||
| chr4:158595436 | G | T | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.286+1937G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158595436 | |||||||
| chr4:158595449 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.286+1950C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158595449 | |||||||
| chr4:158595609 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.286+2110G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158595609 | |||||||
| chr4:158595974 | A | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.286+2475A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158595974 | |||||||
| chr4:158595986 | CA | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.286+2503delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 158595986 | ||||||
| chr4:158596265 | A | AT | 90 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.286+2781dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 158596265 | ||||||
| chr4:158596280 | T | G | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+2781T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158596280 | |||||||
| chr4:158596461 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.287-2865C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158596461 | |||||||
| chr4:158596583 | C | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0187 |
2 | HG00280.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.287-2743C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158596583 | |||||||
| chr4:158596762 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-2564C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158596762 | |||||||
| chr4:158596869 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.287-2457G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158596869 | |||||||
| chr4:158596977 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.287-2349A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158596977 | |||||||
| chr4:158597154 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.287-2172G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158597154 | |||||||
| chr4:158597516 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.287-1810C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158597516 | |||||||
| chr4:158597736 | A | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.287-1590A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158597736 | |||||||
| chr4:158597894 | C | T | 15 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(12): Show |
15 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-1432C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158597894 | |||||||
| chr4:158598416 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.287-910G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158598416 | |||||||
| chr4:158598693 | C | A | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.287-633C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158598693 | |||||||
| chr4:158598824 | T | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0131 |
2 | HG01943.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.287-502T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158598824 | |||||||
| chr4:158598880 | T | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-446T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158598880 | |||||||
| chr4:158598941 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.287-385G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158598941 | |||||||
| chr4:158599086 | T | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0203 a0003c0003t0001g0005 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-240T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158599086 | |||||||
| chr4:158599096 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.287-230C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 3/17 | chr4 | 158599096 | |||||||
| chr4:158599940 | T | C | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.392+509T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158599940 | |||||||
| chr4:158600020 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0075 a0005c0004t0001g0120 |
3 | HG01071.hp2 HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.392+589C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158600020 | |||||||
| chr4:158600328 | TC | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.392+899delC | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158600328 | ||||||
| chr4:158600391 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.392+960A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158600391 | |||||||
| chr4:158600416 | CAG | C | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.392+988_392+989del others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158600416 | ||||||
| chr4:158600518 | C | CT | 3 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0024 |
3 | HG01361.hp1 HG01433.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.392+1087_392+1088i others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158600518 | |||||||
| chr4:158600663 | C | CA | 5 | a0001c0001t0001g0199 a0001c0001t0002g0114 a0001c0001t0002g0115 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.392+1241dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158600663 | ||||||
| chr4:158600826 | C | CA | 17 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0017 others(14): Show |
18 | HG00558.hp1 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.392+1407dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158600826 | ||||||
| chr4:158600829 | A | AC | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
100 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.392+1398_392+1399i others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158600829 | |||||||
| chr4:158600833 | A | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.392+1402A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158600833 | |||||||
| chr4:158600834 | A | G | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.392+1403A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158600834 | |||||||
| chr4:158600875 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.392+1444T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158600875 | |||||||
| chr4:158601080 | G | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.392+1649G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158601080 | |||||||
| chr4:158601129 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.392+1698T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158601129 | |||||||
| chr4:158601163 | C | T | 13 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0143 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.392+1732C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158601163 | |||||||
| chr4:158601201 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.392+1770C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158601201 | |||||||
| chr4:158601479 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.392+2048C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158601479 | |||||||
| chr4:158601863 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.392+2432A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158601863 | |||||||
| chr4:158601895 | A | AT | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.392+2468dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158601895 | ||||||
| chr4:158601931 | A | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0081 a0001c0001t0004g0026 |
3 | HG02809.hp1 HG03516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.392+2500A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158601931 | |||||||
| chr4:158602019 | C | A | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.392+2588C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158602019 | |||||||
| chr4:158602206 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.392+2775T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158602206 | |||||||
| chr4:158602456 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.393-2612C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158602456 | |||||||
| chr4:158602561 | CA | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
116 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.393-2496delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158602561 | ||||||
| chr4:158602679 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.393-2389T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158602679 | |||||||
| chr4:158602808 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG02129.hp1 HG02602.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-2260C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158602808 | |||||||
| chr4:158602870 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.393-2198C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158602870 | |||||||
| chr4:158602888 | A | G | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.393-2180A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158602888 | |||||||
| chr4:158602924 | T | G | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.393-2144T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158602924 | |||||||
| chr4:158603004 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.393-2064C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158603004 | |||||||
| chr4:158603557 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01884.hp2 HG01943.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-1511C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158603557 | |||||||
| chr4:158603833 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.393-1235T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158603833 | |||||||
| chr4:158603889 | C | CAAT | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
40 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.393-1141_393-1139d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158603889 | ||||||
| chr4:158603889 | C | CAATAAT | 3 | a0001c0001t0001g0032 a0001c0001t0001g0083 a0001c0001t0001g0176 |
3 | HG01099.hp1 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.393-1144_393-1139d others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158603889 | ||||||
| chr4:158603889 | C | CAATAATA others(5): Show |
1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.393-1150_393-1139d others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158603889 | ||||||
| chr4:158603889 | CAAT | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
25 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.393-1141_393-1139d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158603889 | ||||||
| chr4:158603889 | CAATAAT | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.393-1144_393-1139d others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158603889 | ||||||
| chr4:158603889 | CAATAATA others(5): Show |
C | 4 | a0001c0001t0001g0096 a0002c0002t0001g0101 a0002c0002t0001g0102 others(1): Show |
4 | HG02735.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.393-1150_393-1139d others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158603889 | ||||||
| chr4:158603899 | A | AATAATG | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.393-1164_393-1163i others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 158603899 | ||||||
| chr4:158603943 | T | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.393-1125T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158603943 | |||||||
| chr4:158604129 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.393-939A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158604129 | |||||||
| chr4:158604222 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.393-846G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158604222 | |||||||
| chr4:158604624 | T | A | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.393-444T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 4/17 | chr4 | 158604624 | |||||||
| chr4:158605223 | C | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+84C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158605223 | |||||||
| chr4:158605224 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+85A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158605224 | |||||||
| chr4:158605357 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.464+218A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158605357 | |||||||
| chr4:158605507 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.464+368G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158605507 | |||||||
| chr4:158605538 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.464+399G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158605538 | |||||||
| chr4:158605721 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.464+582G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158605721 | |||||||
| chr4:158606399 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.464+1260T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606399 | |||||||
| chr4:158606445 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.464+1306C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606445 | |||||||
| chr4:158606580 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0001t0001g0068 |
3 | HG01168.hp1 HG01261.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.465-1392G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606580 | |||||||
| chr4:158606679 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.465-1293A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606679 | |||||||
| chr4:158606686 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0119 |
3 | HG00140.hp2 HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.465-1286T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606686 | |||||||
| chr4:158606746 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0156 a0001c0001t0001g0192 |
3 | HG02523.hp2 HG03669.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.465-1226G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606746 | |||||||
| chr4:158606757 | T | A | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465-1215T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606757 | |||||||
| chr4:158606798 | C | A | 1 | a0001c0001t0001g0004 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.465-1174C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606798 | |||||||
| chr4:158606800 | G | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.465-1172G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606800 | |||||||
| chr4:158606893 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.465-1079A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158606893 | |||||||
| chr4:158607171 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.465-801A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158607171 | |||||||
| chr4:158607184 | G | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0157 a0001c0001t0001g0193 |
3 | HG03098.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.465-788G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158607184 | |||||||
| chr4:158607312 | C | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.465-660C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158607312 | |||||||
| chr4:158607327 | GT | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.465-637delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 158607327 | ||||||
| chr4:158607494 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.465-478G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158607494 | |||||||
| chr4:158607838 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.465-134T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | chr4 | 158607838 | |||||||
| chr4:158607939 | A | AT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.465-24dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 158607939 | ||||||
| chr4:158608162 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.536+119A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158608162 | |||||||
| chr4:158608195 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.536+152G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158608195 | |||||||
| chr4:158608279 | C | CT | 39 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(36): Show |
40 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.536+264dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 158608279 | ||||||
| chr4:158608279 | C | CTT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.536+263_536+264dup others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 158608279 | ||||||
| chr4:158608279 | C | CTTT | 8 | a0001c0001t0001g0040 a0001c0001t0001g0118 a0001c0001t0001g0128 others(5): Show |
8 | HG02055.hp2 HG02129.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.536+262_536+264dup others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 158608279 | ||||||
| chr4:158608279 | CT | C | 9 | a0001c0001t0001g0047 a0001c0001t0001g0060 a0001c0001t0001g0065 others(6): Show |
9 | HG01074.hp2 HG01981.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.536+264delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 158608279 | ||||||
| chr4:158608401 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.536+358C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158608401 | |||||||
| chr4:158608536 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.536+493A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158608536 | |||||||
| chr4:158608742 | A | T | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.536+699A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158608742 | |||||||
| chr4:158608758 | T | G | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.536+715T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158608758 | |||||||
| chr4:158609071 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.536+1028G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158609071 | |||||||
| chr4:158609449 | T | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | NA18986.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.536+1406T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158609449 | |||||||
| chr4:158609561 | G | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
117 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.536+1518G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158609561 | |||||||
| chr4:158609693 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.536+1650A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158609693 | |||||||
| chr4:158609833 | A | G | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.536+1790A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158609833 | |||||||
| chr4:158609939 | A | G | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.536+1896A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158609939 | |||||||
| chr4:158610137 | C | T | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.537-1993C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158610137 | |||||||
| chr4:158610235 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0024 |
2 | HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.537-1895A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158610235 | |||||||
| chr4:158610254 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.537-1876G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158610254 | |||||||
| chr4:158610552 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.537-1578T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158610552 | |||||||
| chr4:158610604 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.537-1526T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158610604 | |||||||
| chr4:158611293 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.537-837G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 6/17 | chr4 | 158611293 | |||||||
| chr4:158612207 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.608+6T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 7/17 | chr4 | 158612207 | |||||||
| chr4:158612398 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.680+36G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158612398 | |||||||
| chr4:158612440 | T | C | 8 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(5): Show |
8 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.680+78T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158612440 | |||||||
| chr4:158612451 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.680+89T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158612451 | |||||||
| chr4:158612799 | C | T | 1 | a0001c0001t0005g0052 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.680+437C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158612799 | |||||||
| chr4:158613105 | AT | A | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.680+744delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158613105 | |||||||
| chr4:158613182 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.680+820G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158613182 | |||||||
| chr4:158613562 | A | C | 1 | a0001c0001t0005g0052 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.680+1200A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158613562 | |||||||
| chr4:158613611 | C | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.680+1249C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158613611 | |||||||
| chr4:158613792 | G | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0086 a0001c0001t0001g0093 |
3 | HG00733.hp2 HG01123.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.680+1430G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158613792 | |||||||
| chr4:158613869 | G | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+1507G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158613869 | |||||||
| chr4:158614117 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+1755C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614117 | |||||||
| chr4:158614161 | T | A | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.680+1799T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614161 | |||||||
| chr4:158614190 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.680+1828C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614190 | |||||||
| chr4:158614217 | T | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.680+1855T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614217 | |||||||
| chr4:158614237 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.680+1875G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614237 | |||||||
| chr4:158614455 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.680+2093C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614455 | |||||||
| chr4:158614524 | T | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+2162T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614524 | |||||||
| chr4:158614551 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.680+2189T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614551 | |||||||
| chr4:158614705 | G | C | 1 | a0001c0001t0005g0052 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.680+2343G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158614705 | |||||||
| chr4:158615067 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.681-2064A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158615067 | |||||||
| chr4:158615326 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.681-1805C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158615326 | |||||||
| chr4:158615781 | CA | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.681-1339delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 158615781 | ||||||
| chr4:158616064 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.681-1067G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158616064 | |||||||
| chr4:158616434 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.681-697G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158616434 | |||||||
| chr4:158616454 | T | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0178 |
2 | HG00735.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.681-677T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158616454 | |||||||
| chr4:158616553 | A | AT | 5 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0063 others(2): Show |
5 | HG02809.hp1 HG03516.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.681-559dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 158616553 | ||||||
| chr4:158616553 | AT | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0016 others(35): Show |
39 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.681-559delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 158616553 | ||||||
| chr4:158616553 | ATT | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(101): Show |
106 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.681-560_681-559del others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 158616553 | ||||||
| chr4:158616553 | ATTT | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0172 others(3): Show |
6 | HG02109.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-561_681-559del others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 158616553 | ||||||
| chr4:158616556 | T | C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-575T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158616556 | |||||||
| chr4:158616677 | G | T | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.681-454G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158616677 | |||||||
| chr4:158616863 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.681-268G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158616863 | |||||||
| chr4:158616900 | G | A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-231G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | chr4 | 158616900 | |||||||
| chr4:158616988 | C | CA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(16): Show |
20 | HG00735.hp1 HG01261.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.681-127dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 158616988 | ||||||
| chr4:158616988 | CA | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(68): Show |
72 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.681-127delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 158616988 | ||||||
| chr4:158617051 | G | GAAT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.681-69_681-67dupAT others(1): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 158617051 | ||||||
| chr4:158617419 | C | CA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(62): Show |
66 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.755+222dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158617419 | ||||||
| chr4:158617419 | C | CAA | 11 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0127 others(8): Show |
11 | HG01981.hp2 HG02258.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.755+221_755+222dup others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158617419 | ||||||
| chr4:158617426 | A | AAAAT | 6 | a0001c0001t0001g0117 a0001c0001t0001g0172 a0001c0001t0001g0173 others(3): Show |
6 | HG02257.hp2 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.755+222_755+223ins others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158617426 | ||||||
| chr4:158617426 | A | AAATAT | 4 | a0001c0001t0001g0002 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
5 | HG00735.hp1 HG01884.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+222_755+223ins others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158617426 | ||||||
| chr4:158617428 | T | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.755+223T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158617428 | |||||||
| chr4:158617430 | T | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(92): Show |
96 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.755+225T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158617430 | |||||||
| chr4:158617432 | T | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(45): Show |
49 | HG00099.hp2 HG00280.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.755+227T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158617432 | |||||||
| chr4:158617434 | T | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0118 a0001c0001t0001g0124 others(13): Show |
16 | HG02055.hp2 HG02129.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.755+229T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158617434 | |||||||
| chr4:158617436 | T | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0153 |
3 | HG02630.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.755+231T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158617436 | |||||||
| chr4:158617501 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.755+296C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158617501 | |||||||
| chr4:158617538 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0090 others(1): Show |
4 | HG00733.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+333T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158617538 | |||||||
| chr4:158617607 | A | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0172 others(3): Show |
6 | HG02895.hp1 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.755+402A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158617607 | |||||||
| chr4:158617625 | AATC | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.755+423_755+425del others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158617625 | ||||||
| chr4:158618003 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.755+798A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158618003 | |||||||
| chr4:158618286 | C | A | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.755+1081C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158618286 | |||||||
| chr4:158618699 | CT | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0205 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.755+1495delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158618699 | |||||||
| chr4:158618812 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.755+1607G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158618812 | |||||||
| chr4:158618822 | A | C | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.755+1617A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158618822 | |||||||
| chr4:158619070 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.755+1865G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158619070 | |||||||
| chr4:158619674 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0090 others(1): Show |
4 | HG00733.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+2469T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158619674 | |||||||
| chr4:158619692 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.755+2487G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158619692 | |||||||
| chr4:158619754 | G | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.755+2549G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158619754 | |||||||
| chr4:158619881 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.755+2676C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158619881 | |||||||
| chr4:158619885 | T | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.755+2680T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158619885 | |||||||
| chr4:158620251 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.755+3046A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158620251 | |||||||
| chr4:158620445 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.755+3240C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158620445 | |||||||
| chr4:158620494 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.755+3289T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158620494 | |||||||
| chr4:158620600 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
117 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.755+3395A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158620600 | |||||||
| chr4:158620612 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.755+3407T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158620612 | |||||||
| chr4:158620643 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.755+3438G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158620643 | |||||||
| chr4:158621031 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.755+3826G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621031 | |||||||
| chr4:158621044 | A | G | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.755+3839A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621044 | |||||||
| chr4:158621054 | C | CA | 4 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG03516.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.755+3849_755+3850i others(3): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621054 | |||||||
| chr4:158621095 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
117 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.755+3890A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621095 | |||||||
| chr4:158621109 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.755+3904G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621109 | |||||||
| chr4:158621229 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.755+4024G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621229 | |||||||
| chr4:158621352 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.755+4147G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621352 | |||||||
| chr4:158621726 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.755+4521T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621726 | |||||||
| chr4:158621819 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.755+4614A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158621819 | |||||||
| chr4:158622085 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
115 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.756-4735T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158622085 | |||||||
| chr4:158622163 | T | C | 7 | a0001c0001t0002g0033 a0001c0001t0002g0109 a0001c0001t0002g0114 others(4): Show |
7 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-4657T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158622163 | |||||||
| chr4:158622314 | T | TA | 16 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0154 others(13): Show |
16 | HG01123.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.756-4495dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158622314 | ||||||
| chr4:158622461 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.756-4359G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158622461 | |||||||
| chr4:158622581 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.756-4239G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158622581 | |||||||
| chr4:158622794 | T | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.756-4026T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158622794 | |||||||
| chr4:158622838 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.756-3982A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158622838 | |||||||
| chr4:158622924 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
117 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.756-3896G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158622924 | |||||||
| chr4:158623305 | C | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.756-3515C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623305 | |||||||
| chr4:158623335 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.756-3485C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623335 | |||||||
| chr4:158623340 | T | TAA | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0131 |
3 | HG01884.hp2 HG01943.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.756-3479_756-3478i others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623340 | ||||||
| chr4:158623342 | C | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0131 |
3 | HG01884.hp2 HG01943.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.756-3478C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623342 | |||||||
| chr4:158623342 | C | CA | 29 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(26): Show |
30 | HG00735.hp1 HG01981.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.756-3461dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623342 | ||||||
| chr4:158623342 | C | CAA | 38 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(35): Show |
38 | HG01123.hp1 HG01884.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.756-3462_756-3461d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623342 | ||||||
| chr4:158623342 | C | CAAA | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0074 others(24): Show |
28 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.756-3463_756-3461d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623342 | ||||||
| chr4:158623342 | C | CAAAA | 15 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0099 others(12): Show |
15 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.756-3464_756-3461d others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623342 | ||||||
| chr4:158623386 | CA | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0065 |
2 | HG01074.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.756-3433delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623386 | |||||||
| chr4:158623449 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.756-3371C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623449 | |||||||
| chr4:158623485 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.756-3335A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623485 | |||||||
| chr4:158623502 | C | CA | 14 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(11): Show |
14 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.756-3294dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAA | 11 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0021 others(8): Show |
11 | HG00558.hp1 HG00558.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.756-3297_756-3294d others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAA | 8 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0042 others(5): Show |
9 | HG00741.hp1 HG01168.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.756-3298_756-3294d others(7): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0198 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.756-3303_756-3294d others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(4): Show |
2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.756-3304_756-3294d others(13): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.756-3306_756-3294d others(15): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0089 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.756-3309_756-3294d others(18): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(10): Show |
8 | a0001c0001t0001g0044 a0001c0001t0001g0077 a0001c0001t0001g0079 others(5): Show |
8 | HG01123.hp2 HG01261.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.756-3310_756-3294d others(19): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0154 |
2 | HG02486.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.756-3311_756-3294d others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0086 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.756-3312_756-3294d others(21): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.756-3314_756-3294d others(23): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0020 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.756-3316_756-3294d others(25): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.756-3294_756-3293i others(38): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | CA | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0084 others(4): Show |
7 | HG00438.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-3294delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | CAA | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0034 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.756-3295_756-3294d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | CAAA | C | 6 | a0001c0001t0001g0157 a0001c0001t0001g0193 a0001c0001t0003g0030 others(3): Show |
6 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.756-3296_756-3294d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623502 | CAAAA | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(70): Show |
74 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.756-3297_756-3294d others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158623502 | ||||||
| chr4:158623545 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.756-3275A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623545 | |||||||
| chr4:158623627 | A | G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0203 a0003c0003t0001g0005 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-3193A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623627 | |||||||
| chr4:158623641 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.756-3179A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623641 | |||||||
| chr4:158623768 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.756-3052G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623768 | |||||||
| chr4:158623960 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.756-2860T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623960 | |||||||
| chr4:158623996 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(91): Show |
96 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.756-2824G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158623996 | |||||||
| chr4:158624035 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 |
3 | HG02109.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.756-2785G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624035 | |||||||
| chr4:158624057 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0004g0162 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.756-2763G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624057 | |||||||
| chr4:158624117 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.756-2703A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624117 | |||||||
| chr4:158624339 | A | C | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.756-2481A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624339 | |||||||
| chr4:158624572 | C | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.756-2248C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624572 | |||||||
| chr4:158624584 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.756-2236G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624584 | |||||||
| chr4:158624601 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0001t0001g0068 |
3 | HG01168.hp1 HG01261.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.756-2219A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624601 | |||||||
| chr4:158624606 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.756-2214C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624606 | |||||||
| chr4:158624754 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.756-2066G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624754 | |||||||
| chr4:158624789 | G | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.756-2031G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624789 | |||||||
| chr4:158624944 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.756-1876G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158624944 | |||||||
| chr4:158625072 | CTT | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.756-1747_756-1746d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158625072 | |||||||
| chr4:158625175 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.756-1645A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158625175 | |||||||
| chr4:158625307 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.756-1513T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158625307 | |||||||
| chr4:158625369 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.756-1451C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158625369 | |||||||
| chr4:158625387 | ACTT | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.756-1430_756-1428d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158625387 | ||||||
| chr4:158625423 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.756-1397A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158625423 | |||||||
| chr4:158625790 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.756-1030C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158625790 | |||||||
| chr4:158625990 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.756-830C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158625990 | |||||||
| chr4:158626108 | C | CTAGATAG others(57): Show |
1 | a0006c0005t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.756-710_756-709ins others(64): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626108 | ||||||
| chr4:158626108 | CTATA | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0161 a0001c0001t0001g0172 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.756-709_756-706del others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626108 | ||||||
| chr4:158626108 | CTATATAG others(1): Show |
C | 14 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0124 others(11): Show |
14 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-709_756-702del others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626108 | ||||||
| chr4:158626108 | CTATATAG others(5): Show |
C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0154 a0001c0001t0001g0173 others(7): Show |
11 | HG00735.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.756-709_756-698del others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626108 | ||||||
| chr4:158626108 | CTATATAG others(9): Show |
C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0159 a0001c0001t0001g0176 |
3 | HG02257.hp2 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.756-709_756-694del others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626108 | ||||||
| chr4:158626111 | T | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(78): Show |
82 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.756-709T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626111 | |||||||
| chr4:158626111 | T | TATAG | 8 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0060 others(5): Show |
8 | HG02523.hp1 NA18947.hp1 NA18993.hp2 others(5): Show |
intron_variant | MODIFIER | c.756-646_756-643dup others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626111 | ||||||
| chr4:158626111 | TATAG | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0017 others(26): Show |
29 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.756-646_756-643del others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626111 | ||||||
| chr4:158626111 | TATAGATA others(1): Show |
T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(15): Show |
18 | HG00099.hp1 HG00738.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.756-650_756-643del others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626111 | ||||||
| chr4:158626111 | TATAGATA others(5): Show |
T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0042 others(7): Show |
10 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.756-654_756-643del others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626111 | ||||||
| chr4:158626111 | TATAGATA others(9): Show |
T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0073 a0001c0001t0001g0087 others(2): Show |
5 | HG00558.hp1 HG00558.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-658_756-643del others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626111 | ||||||
| chr4:158626111 | TATAGATA others(13): Show |
T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0090 |
2 | HG00733.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.756-662_756-643del others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626111 | ||||||
| chr4:158626120 | A | ATAGATAG others(37): Show |
1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.756-657_756-656ins others(44): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626120 | ||||||
| chr4:158626144 | A | ATAGATAG others(17): Show |
1 | a0001c0001t0001g0004 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.756-653_756-652ins others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626144 | ||||||
| chr4:158626144 | A | ATAGATAG others(13): Show |
3 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0002g0181 |
3 | HG02886.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.756-657_756-656ins others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626144 | ||||||
| chr4:158626144 | A | ATAGATAG others(9): Show |
2 | a0001c0001t0001g0145 a0001c0001t0002g0115 |
2 | HG00738.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.756-661_756-660ins others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626144 | ||||||
| chr4:158626144 | A | ATAGATAG others(5): Show |
4 | a0001c0001t0001g0098 a0001c0001t0001g0148 a0001c0001t0002g0114 others(1): Show |
4 | HG01168.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-665_756-664ins others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626144 | ||||||
| chr4:158626144 | A | ATAGATAG others(1): Show |
3 | a0001c0001t0001g0095 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG00639.hp1 HG01074.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.756-669_756-668ins others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626144 | ||||||
| chr4:158626148 | A | ATAGATAG others(21): Show |
1 | a0001c0001t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.756-645_756-644ins others(28): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626148 | ||||||
| chr4:158626148 | A | ATAGATAG others(17): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0160 |
3 | HG02258.hp2 HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.756-649_756-648ins others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626148 | ||||||
| chr4:158626148 | A | ATAGATAG others(13): Show |
6 | a0001c0001t0001g0074 a0001c0001t0001g0105 a0001c0001t0001g0118 others(3): Show |
6 | HG01099.hp2 HG01517.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.756-653_756-652ins others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626148 | ||||||
| chr4:158626148 | A | ATAGATAG others(9): Show |
8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0112 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.756-657_756-656ins others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626148 | ||||||
| chr4:158626148 | A | ATAGATAG others(5): Show |
9 | a0001c0001t0001g0027 a0001c0001t0001g0096 a0001c0001t0001g0100 others(6): Show |
9 | HG02055.hp2 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.756-661_756-660ins others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626148 | ||||||
| chr4:158626148 | A | ATAGATAG others(1): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0110 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.756-665_756-664ins others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626148 | ||||||
| chr4:158626148 | A | ATAGT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0097 others(7): Show |
11 | HG00642.hp2 HG00741.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.756-669_756-668ins others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 158626148 | ||||||
| chr4:158626148 | A | T | 8 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0128 others(5): Show |
8 | HG01884.hp2 HG01943.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.756-672A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626148 | |||||||
| chr4:158626354 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(30): Show |
34 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.756-466G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626354 | |||||||
| chr4:158626379 | G | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0049 others(1): Show |
4 | NA18986.hp2 NA18993.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-441G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626379 | |||||||
| chr4:158626455 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.756-365G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626455 | |||||||
| chr4:158626486 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.756-334A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626486 | |||||||
| chr4:158626499 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.756-321G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626499 | |||||||
| chr4:158626530 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.756-290T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626530 | |||||||
| chr4:158626568 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.756-252T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626568 | |||||||
| chr4:158626600 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.756-220G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 9/17 | chr4 | 158626600 | |||||||
| chr4:158626948 | A | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.827+57A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158626948 | |||||||
| chr4:158627076 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.827+185T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158627076 | |||||||
| chr4:158627109 | AAT | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.827+220_827+221del others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627109 | ||||||
| chr4:158627145 | G | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.827+254G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158627145 | |||||||
| chr4:158627157 | C | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(30): Show |
34 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.827+266C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158627157 | |||||||
| chr4:158627254 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.827+363T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158627254 | |||||||
| chr4:158627504 | G | GGTGT | 5 | a0001c0001t0001g0175 a0001c0001t0003g0030 a0001c0001t0003g0036 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+656_827+659dup others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | G | GGTGTGT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
9 | HG01884.hp1 HG01981.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.827+654_827+659dup others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0154 a0001c0001t0001g0159 a0001c0001t0001g0176 others(3): Show |
6 | HG00735.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.827+652_827+659dup others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | G | GGTGTGTG others(3): Show |
5 | a0001c0001t0001g0117 a0001c0001t0001g0172 a0001c0001t0001g0174 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.827+650_827+659dup others(10): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0001g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.827+648_827+659dup others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | GGT | G | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0044 others(23): Show |
26 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.827+658_827+659del others(2): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | GGTGT | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.827+656_827+659del others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | GGTGTGT | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0040 others(46): Show |
50 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.827+654_827+659del others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | GGTGTGTG others(1): Show |
G | 16 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(13): Show |
16 | HG00733.hp2 HG01081.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.827+652_827+659del others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | GGTGTGTG others(3): Show |
G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.827+650_827+659del others(10): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.827+648_827+659del others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627504 | GGTGTGTG others(7): Show |
G | 7 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0132 others(4): Show |
7 | HG01123.hp1 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.827+646_827+659del others(14): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 158627504 | ||||||
| chr4:158627634 | C | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0187 |
2 | HG00280.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.827+743C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158627634 | |||||||
| chr4:158627648 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.827+757C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158627648 | |||||||
| chr4:158627761 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.827+870C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158627761 | |||||||
| chr4:158627791 | G | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0063 others(2): Show |
5 | HG02809.hp1 HG03516.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.828-847G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158627791 | |||||||
| chr4:158628029 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.828-609C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158628029 | |||||||
| chr4:158628047 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.828-591T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158628047 | |||||||
| chr4:158628219 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0157 a0001c0001t0001g0193 |
3 | HG03098.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.828-419G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158628219 | |||||||
| chr4:158628380 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.828-258G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 10/17 | chr4 | 158628380 | |||||||
| chr4:158628813 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.899+104C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158628813 | |||||||
| chr4:158628943 | T | TAAGGCCG others(307): Show |
1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.899+236_899+237ins others(314): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(296): Show |
3 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0153 |
3 | HG02809.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.899+236_899+237ins others(303): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(297): Show |
3 | a0001c0001t0001g0112 a0001c0001t0001g0126 a0001c0001t0001g0134 |
3 | HG02630.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.899+236_899+237ins others(304): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(299): Show |
1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.899+236_899+237ins others(306): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(302): Show |
1 | a0001c0001t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.899+236_899+237ins others(309): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(283): Show |
1 | a0001c0001t0001g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.899+236_899+237ins others(290): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(289): Show |
3 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0002c0002t0001g0103 |
3 | HG01099.hp2 HG02886.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.899+236_899+237ins others(296): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(290): Show |
1 | a0002c0002t0001g0102 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.899+236_899+237ins others(297): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(291): Show |
3 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0127 |
3 | HG02723.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.899+236_899+237ins others(298): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(292): Show |
5 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0001g0169 others(2): Show |
5 | HG02129.hp1 HG02602.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.899+236_899+237ins others(299): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(294): Show |
1 | a0001c0001t0001g0131 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.899+236_899+237ins others(301): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(297): Show |
1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.899+236_899+237ins others(304): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(298): Show |
3 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0193 |
3 | HG01884.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.899+236_899+237ins others(305): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(299): Show |
5 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0144 others(2): Show |
5 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(2): Show |
intron_variant | MODIFIER | c.899+236_899+237ins others(306): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(300): Show |
10 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0128 others(7): Show |
10 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.899+236_899+237ins others(307): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(301): Show |
3 | a0001c0001t0001g0104 a0001c0001t0001g0124 a0002c0002t0001g0101 |
3 | HG02735.hp2 NA18906.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.899+236_899+237ins others(308): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(302): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0156 |
2 | HG03669.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.899+236_899+237ins others(309): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(303): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0074 a0001c0001t0001g0096 others(1): Show |
4 | HG01517.hp2 HG03098.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+236_899+237ins others(310): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(304): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0097 a0001c0001t0001g0132 |
3 | HG03098.hp2 NA18906.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.899+236_899+237ins others(311): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(305): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0192 |
4 | NA18947.hp2 NA18994.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+236_899+237ins others(312): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(308): Show |
1 | a0001c0001t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.899+236_899+237ins others(315): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628943 | T | TAAGGCCG others(310): Show |
2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | NA19004.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.899+236_899+237ins others(317): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158628943 | ||||||
| chr4:158628946 | T | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.899+237T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158628946 | |||||||
| chr4:158628950 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.899+241G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158628950 | |||||||
| chr4:158628951 | C | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.899+242C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158628951 | |||||||
| chr4:158628952 | C | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.899+243C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158628952 | |||||||
| chr4:158628954 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.899+245G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158628954 | |||||||
| chr4:158628955 | T | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.899+246T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158628955 | |||||||
| chr4:158628957 | T | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.899+248T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158628957 | |||||||
| chr4:158629087 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.899+378G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629087 | |||||||
| chr4:158629116 | C | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0090 others(1): Show |
4 | HG00733.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+407C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629116 | |||||||
| chr4:158629163 | G | A | 14 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0111 others(11): Show |
14 | HG02129.hp1 HG02602.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.899+454G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629163 | |||||||
| chr4:158629194 | G | A | 1 | a0001c0001t0005g0052 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.899+485G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629194 | |||||||
| chr4:158629365 | C | T | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+656C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629365 | |||||||
| chr4:158629608 | A | AT | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.899+906dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 158629608 | ||||||
| chr4:158629620 | T | G | 1 | a0001c0001t0001g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.899+911T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629620 | |||||||
| chr4:158629704 | G | A | 4 | a0001c0001t0001g0108 a0001c0001t0001g0161 a0001c0001t0001g0163 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+995G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629704 | |||||||
| chr4:158629723 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
81 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.899+1014A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629723 | |||||||
| chr4:158629890 | T | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
81 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.899+1181T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158629890 | |||||||
| chr4:158630094 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0176 |
2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.899+1385A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158630094 | |||||||
| chr4:158630146 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.899+1437C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158630146 | |||||||
| chr4:158630369 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(33): Show |
37 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.899+1660A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158630369 | |||||||
| chr4:158630433 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.899+1724G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158630433 | |||||||
| chr4:158630612 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(32): Show |
36 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.899+1903C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158630612 | |||||||
| chr4:158630657 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(32): Show |
36 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.899+1948G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158630657 | |||||||
| chr4:158630995 | C | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(32): Show |
36 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.899+2286C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158630995 | |||||||
| chr4:158631956 | G | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.900-1449G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158631956 | |||||||
| chr4:158632194 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | NA18986.hp2 NA19011.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.900-1211G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158632194 | |||||||
| chr4:158632753 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.900-652A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158632753 | |||||||
| chr4:158632859 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.900-546T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158632859 | |||||||
| chr4:158632864 | A | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.900-541A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158632864 | |||||||
| chr4:158632933 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.900-472A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158632933 | |||||||
| chr4:158632964 | G | T | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.900-441G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158632964 | |||||||
| chr4:158633031 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.900-374G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158633031 | |||||||
| chr4:158633125 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.900-280G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158633125 | |||||||
| chr4:158633137 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0155 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.900-268T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158633137 | |||||||
| chr4:158633242 | A | G | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.900-163A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158633242 | |||||||
| chr4:158633765 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.971+289T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158633765 | |||||||
| chr4:158633814 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.971+338C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158633814 | |||||||
| chr4:158634215 | C | G | 1 | a0001c0001t0001g0011 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.971+739C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158634215 | |||||||
| chr4:158634272 | G | C | 1 | a0002c0002t0001g0101 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.971+796G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158634272 | |||||||
| chr4:158634428 | C | A | 3 | a0001c0001t0004g0162 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG02258.hp1 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.971+952C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158634428 | |||||||
| chr4:158634519 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.971+1043T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158634519 | |||||||
| chr4:158634522 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0131 |
3 | HG01884.hp2 HG01943.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+1046T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158634522 | |||||||
| chr4:158634772 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.971+1296A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158634772 | |||||||
| chr4:158634840 | T | C | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.971+1364T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158634840 | |||||||
| chr4:158634974 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.971+1498T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158634974 | |||||||
| chr4:158635286 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.971+1810G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635286 | |||||||
| chr4:158635452 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.971+1976A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635452 | |||||||
| chr4:158635480 | C | A | 1 | a0001c0001t0001g0066 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.971+2004C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635480 | |||||||
| chr4:158635511 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(40): Show |
44 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.971+2035C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635511 | |||||||
| chr4:158635614 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.971+2138G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635614 | |||||||
| chr4:158635625 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+2149T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635625 | |||||||
| chr4:158635655 | T | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(40): Show |
44 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.971+2179T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635655 | |||||||
| chr4:158635758 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.972-2250C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635758 | |||||||
| chr4:158635802 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.972-2206T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635802 | |||||||
| chr4:158635848 | CT | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0032 others(45): Show |
50 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.972-2151delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 158635848 | ||||||
| chr4:158635857 | T | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(37): Show |
41 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.972-2151T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635857 | |||||||
| chr4:158635877 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0193 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.972-2131T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635877 | |||||||
| chr4:158635890 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.972-2118A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158635890 | |||||||
| chr4:158636202 | G | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.972-1806G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636202 | |||||||
| chr4:158636243 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0126 others(6): Show |
9 | HG01081.hp1 HG02055.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.972-1765C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636243 | |||||||
| chr4:158636293 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.972-1715G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636293 | |||||||
| chr4:158636369 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(103): Show |
108 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.972-1639G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636369 | |||||||
| chr4:158636419 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.972-1589T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636419 | |||||||
| chr4:158636511 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0034 others(40): Show |
44 | HG00735.hp1 HG01123.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.972-1497G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636511 | |||||||
| chr4:158636683 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.972-1325G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636683 | |||||||
| chr4:158636762 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.972-1246T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636762 | |||||||
| chr4:158636916 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.972-1092C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158636916 | |||||||
| chr4:158637069 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.972-939A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158637069 | |||||||
| chr4:158637314 | C | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.972-694C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158637314 | |||||||
| chr4:158637332 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG00558.hp2 HG02132.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.972-676A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158637332 | |||||||
| chr4:158637342 | T | A | 1 | a0001c0001t0004g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.972-666T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158637342 | |||||||
| chr4:158637443 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.972-565G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158637443 | |||||||
| chr4:158637573 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.972-435T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158637573 | |||||||
| chr4:158637752 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.972-256A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158637752 | |||||||
| chr4:158637773 | T | G | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0113 others(1): Show |
4 | HG02723.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-235T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 12/17 | chr4 | 158637773 | |||||||
| chr4:158638111 | A | G | 3 | a0001c0001t0004g0162 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG02258.hp1 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1043+32A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 13/17 | chr4 | 158638111 | |||||||
| chr4:158638238 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1043+159C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 13/17 | chr4 | 158638238 | |||||||
| chr4:158638277 | A | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0015 |
2 | NA18993.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1043+198A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 13/17 | chr4 | 158638277 | |||||||
| chr4:158638374 | T | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1043+295T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 13/17 | chr4 | 158638374 | |||||||
| chr4:158638680 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1044-580T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 13/17 | chr4 | 158638680 | |||||||
| chr4:158638811 | C | CA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1044-433dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 158638811 | ||||||
| chr4:158639645 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1115+314G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158639645 | |||||||
| chr4:158639699 | G | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1115+368G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158639699 | |||||||
| chr4:158639731 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1115+400G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158639731 | |||||||
| chr4:158639753 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1115+422A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158639753 | |||||||
| chr4:158639775 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1115+444G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158639775 | |||||||
| chr4:158640052 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1115+721C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640052 | |||||||
| chr4:158640145 | T | C | 7 | a0001c0001t0002g0033 a0001c0001t0002g0109 a0001c0001t0002g0114 others(4): Show |
7 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115+814T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640145 | |||||||
| chr4:158640272 | T | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1115+941T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640272 | |||||||
| chr4:158640340 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1115+1009A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640340 | |||||||
| chr4:158640444 | T | C | 7 | a0001c0001t0002g0033 a0001c0001t0002g0109 a0001c0001t0002g0114 others(4): Show |
7 | HG02280.hp2 HG02818.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115+1113T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640444 | |||||||
| chr4:158640445 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1115+1114C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640445 | |||||||
| chr4:158640504 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02647.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1115+1173G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640504 | |||||||
| chr4:158640963 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1115+1632A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640963 | |||||||
| chr4:158640977 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1115+1646T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158640977 | |||||||
| chr4:158641143 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1115+1812T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158641143 | |||||||
| chr4:158641247 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1115+1916T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158641247 | |||||||
| chr4:158641468 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0063 |
2 | NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1115+2137C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158641468 | |||||||
| chr4:158641733 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1115+2402G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158641733 | |||||||
| chr4:158641758 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1115+2427T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158641758 | |||||||
| chr4:158641860 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1115+2529G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158641860 | |||||||
| chr4:158641995 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1115+2664A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158641995 | |||||||
| chr4:158642020 | T | C | 4 | a0001c0001t0003g0030 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01981.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115+2689T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158642020 | |||||||
| chr4:158642096 | C | CT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+2775dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158642096 | ||||||
| chr4:158642111 | T | C | 3 | a0001c0001t0004g0162 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG02258.hp1 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1115+2780T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158642111 | |||||||
| chr4:158642216 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1116-2693G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158642216 | |||||||
| chr4:158642235 | A | T | 6 | a0001c0001t0001g0074 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG00099.hp2 HG00280.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116-2674A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158642235 | |||||||
| chr4:158642662 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1116-2247C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158642662 | |||||||
| chr4:158642679 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1116-2230A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158642679 | |||||||
| chr4:158642711 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1116-2198T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158642711 | |||||||
| chr4:158642842 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00140.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1116-2067G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158642842 | |||||||
| chr4:158643016 | C | T | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1116-1893C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643016 | |||||||
| chr4:158643151 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0024 others(16): Show |
19 | HG00438.hp2 HG00558.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1116-1758A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643151 | |||||||
| chr4:158643244 | A | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG00735.hp1 HG01884.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.1116-1665A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643244 | |||||||
| chr4:158643285 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1116-1624G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643285 | |||||||
| chr4:158643468 | G | GT | 76 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1116-1422dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158643468 | ||||||
| chr4:158643468 | G | GTT | 81 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1116-1423_1116-142 others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158643468 | ||||||
| chr4:158643468 | G | GTTT | 13 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0044 others(10): Show |
13 | HG00140.hp1 HG01123.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1116-1424_1116-142 others(7): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158643468 | ||||||
| chr4:158643502 | T | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1116-1407T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643502 | |||||||
| chr4:158643531 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1116-1378T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643531 | |||||||
| chr4:158643574 | C | T | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(4): Show |
7 | HG00140.hp1 HG01261.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116-1335C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643574 | |||||||
| chr4:158643576 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1116-1333A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643576 | |||||||
| chr4:158643615 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1116-1294G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643615 | |||||||
| chr4:158643722 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0127 |
3 | HG03516.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1116-1187C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643722 | |||||||
| chr4:158643767 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1116-1142A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643767 | |||||||
| chr4:158643822 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1116-1087G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643822 | |||||||
| chr4:158643855 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02129.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1116-1054C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643855 | |||||||
| chr4:158643960 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1116-949T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643960 | |||||||
| chr4:158644041 | C | CT | 16 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0163 others(13): Show |
16 | HG01123.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1116-848dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158644041 | ||||||
| chr4:158644041 | C | CTT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0198 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116-849_1116-848d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158644041 | ||||||
| chr4:158644041 | CT | C | 5 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0127 others(2): Show |
5 | HG00438.hp1 HG02897.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116-848delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158644041 | ||||||
| chr4:158644041 | CTT | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1116-849_1116-848d others(4): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158644041 | ||||||
| chr4:158644041 | CTTT | C | 6 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0001c0001t0001g0092 others(3): Show |
6 | HG01081.hp2 HG02258.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-850_1116-848d others(5): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 158644041 | ||||||
| chr4:158644085 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0113 others(1): Show |
4 | HG02723.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-824C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644085 | |||||||
| chr4:158644132 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1116-777C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644132 | |||||||
| chr4:158644147 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1116-762C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644147 | |||||||
| chr4:158644193 | C | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.1116-716C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644193 | |||||||
| chr4:158644203 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1116-706C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644203 | |||||||
| chr4:158644258 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1116-651A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644258 | |||||||
| chr4:158644490 | A | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | NA19004.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1116-419A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644490 | |||||||
| chr4:158644553 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1116-356A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644553 | |||||||
| chr4:158644570 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1116-339G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644570 | |||||||
| chr4:158644588 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(59): Show |
63 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1116-321C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644588 | |||||||
| chr4:158644599 | C | T | 3 | a0001c0001t0004g0026 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG03139.hp2 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1116-310C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644599 | |||||||
| chr4:158644605 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1116-304C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644605 | |||||||
| chr4:158644736 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(58): Show |
62 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1116-173G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644736 | |||||||
| chr4:158645400 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1345+262C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158645400 | |||||||
| chr4:158645405 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1345+267G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158645405 | |||||||
| chr4:158645440 | C | A | 4 | a0001c0001t0004g0026 a0001c0001t0004g0162 a0001c0001t0004g0204 others(1): Show |
4 | HG02258.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345+302C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158645440 | |||||||
| chr4:158645537 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1345+399C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158645537 | |||||||
| chr4:158645551 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1345+413C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158645551 | |||||||
| chr4:158645566 | A | C | 1 | a0001c0001t0001g0014 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1345+428A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158645566 | |||||||
| chr4:158645961 | G | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1345+823G>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158645961 | |||||||
| chr4:158646180 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1346-611T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158646180 | |||||||
| chr4:158646331 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1346-460T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158646331 | |||||||
| chr4:158646364 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1346-427A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158646364 | |||||||
| chr4:158646736 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1346-55T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158646736 | |||||||
| chr4:158646784 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | splice_region_variant&intron_variant | LOW | c.1346-7C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 15/17 | chr4 | 158646784 | |||||||
| chr4:158647231 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1756+30A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | chr4 | 158647231 | |||||||
| chr4:158647508 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1756+307T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | chr4 | 158647508 | |||||||
| chr4:158647887 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1757-612G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | chr4 | 158647887 | |||||||
| chr4:158647891 | C | A | 12 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(9): Show |
12 | HG02109.hp2 HG02280.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1757-608C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | chr4 | 158647891 | |||||||
| chr4:158648014 | C | CA | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1757-472dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 158648014 | ||||||
| chr4:158648175 | A | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG00140.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1757-324A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | chr4 | 158648175 | |||||||
| chr4:158648181 | A | AT | 12 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(9): Show |
12 | HG02109.hp2 HG02280.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1757-316dupT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 158648181 | ||||||
| chr4:158648325 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1757-174T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | chr4 | 158648325 | |||||||
| chr4:158648375 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1757-124A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | chr4 | 158648375 | |||||||
| chr4:158648942 | AT | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1975+226delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158648942 | |||||||
| chr4:158648954 | A | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1975+237A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158648954 | |||||||
| chr4:158648987 | G | A | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1975+270G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158648987 | |||||||
| chr4:158649100 | CA | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1975+395delA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158649100 | ||||||
| chr4:158649249 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1975+532G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158649249 | |||||||
| chr4:158649551 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1975+834C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158649551 | |||||||
| chr4:158649567 | C | T | 4 | a0001c0001t0004g0026 a0001c0001t0004g0162 a0001c0001t0004g0204 others(1): Show |
4 | HG02258.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+850C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158649567 | |||||||
| chr4:158649617 | AT | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1975+901delT | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158649617 | |||||||
| chr4:158649678 | T | TA | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1975+968dupA | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158649678 | ||||||
| chr4:158650036 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1975+1319A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650036 | |||||||
| chr4:158650146 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1975+1429C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650146 | |||||||
| chr4:158650206 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1975+1489C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650206 | |||||||
| chr4:158650221 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1975+1504G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650221 | |||||||
| chr4:158650236 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1975+1519A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650236 | |||||||
| chr4:158650281 | AATC | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1976-1473_1976-147 others(7): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650281 | ||||||
| chr4:158650325 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1976-1432C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650325 | |||||||
| chr4:158650373 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0100 |
2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1976-1384T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650373 | |||||||
| chr4:158650385 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1976-1372C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650385 | |||||||
| chr4:158650432 | A | AAT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
24 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1976-1307_1976-130 others(6): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | AATAT | 2 | a0001c0001t0001g0134 a0001c0001t0001g0203 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1976-1309_1976-130 others(8): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | AATATAT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0040 others(36): Show |
40 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1976-1311_1976-130 others(10): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | AATATATA others(1): Show |
5 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0112 others(2): Show |
5 | HG01081.hp1 NA18994.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.1976-1313_1976-130 others(12): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | AATATATA others(5): Show |
6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0113 others(3): Show |
6 | HG02723.hp1 HG02922.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1976-1317_1976-130 others(16): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | AATATATA others(7): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0118 a0001c0001t0001g0171 others(1): Show |
4 | HG02129.hp1 HG02602.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976-1319_1976-130 others(18): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | AATATATA others(25): Show |
1 | a0001c0001t0001g0004 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1976-1310_1976-130 others(36): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | AATATATA others(9): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0170 |
2 | HG03098.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1976-1321_1976-130 others(20): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | AATATATA others(13): Show |
1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1976-1306_1976-130 others(24): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 158650432 | ||||||
| chr4:158650432 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1976-1325_1976-132 others(19): Show |
RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650432 | |||||||
| chr4:158650450 | T | A | 12 | a0001c0001t0001g0032 a0001c0001t0001g0108 a0001c0001t0001g0161 others(9): Show |
12 | HG02109.hp2 HG02280.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1976-1307T>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650450 | |||||||
| chr4:158650484 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1976-1273T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650484 | |||||||
| chr4:158650675 | C | G | 3 | a0001c0001t0001g0203 a0003c0003t0001g0005 a0003c0003t0001g0006 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1976-1082C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650675 | |||||||
| chr4:158650723 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0132 |
3 | HG02922.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1976-1034T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650723 | |||||||
| chr4:158650750 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1976-1007T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158650750 | |||||||
| chr4:158651494 | A | G | 2 | a0003c0003t0001g0005 a0003c0003t0001g0006 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1976-263A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158651494 | |||||||
| chr4:158651683 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1976-74G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158651683 | |||||||
| chr4:158651706 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1976-51T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158651706 |