Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr4 | 158516882 | 158658372 |
| a0002 | 0/0 | 757 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0003 | 0/0 | 757 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0004 | 0/0 | 757 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0005 | 0/0 | 757 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0006 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2274 | 202 | 81 | 41 | 47 | 10 | 21 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| c0002 | 0/0 | 2274 | 3 | 0 | 0 | 0 | 0 | 3 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| c0003 | 0/0 | 2274 | 2 | 2 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| c0004 | 0/0 | 2274 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| c0005 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| c0006 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1413 | 192 | 69 | 41 | 46 | 10 | 24 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| t0002 | 0/0 | 1410 | 7 | 7 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| t0003 | 0/0 | 1413 | 5 | 4 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| t0004 | 0/0 | 1415 | 4 | 4 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| t0005 | 0/0 | 1413 | 2 | 0 | 0 | 2 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2274 | 202 | 81 | 41 | 47 | 10 | 21 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0002c0002 | 0/0 | 2274 | 3 | 0 | 0 | 0 | 0 | 3 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0003c0003 | 0/0 | 2274 | 2 | 2 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0004c0006 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0005c0004 | 0/0 | 2274 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0006c0005 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | 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 | copy fasta | chr4 | 158516882 | 158658372 |
| a0001c0001t0002 | 0/0 | 3683 | 6 | 6 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0001c0001t0003 | 0/0 | 3686 | 5 | 4 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0001c0001t0004 | 0/0 | 3688 | 4 | 4 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0001c0001t0005 | 0/0 | 3686 | 2 | 0 | 0 | 2 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0002c0002t0001 | 0/0 | 3686 | 3 | 0 | 0 | 0 | 0 | 3 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0003c0003t0001 | 0/0 | 3686 | 2 | 2 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0004c0006t0001 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0005c0004t0001 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| a0006c0005t0002 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | copy fasta | chr4 | 158516882 | 158658372 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0006 | 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 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0064 | 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 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0073 | 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 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0103 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0109 | 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 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0162 | 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 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 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 | 0/0 | 1 | 1 | 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 | 1/0 | 1 | 0 | 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 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0002g0113 | 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 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0003c0003t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0003c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0004c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0005c0004t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| a0006c0005t0002g0209 | 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 | g0188 | EUR | GBR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00438 | hp1 | a0004 | c0006 | t0001 | g0074 | EAS | CHS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0014 | 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 | g0098 | 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 | g0016 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0023 | 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 | g0143 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01071 | hp2 | a0005 | c0004 | t0001 | g0118 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0073 | 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 | g0127 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0159 | 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 | g0119 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0004 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0205 | 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 | g0100 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | 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 | g0168 | SAS | PJL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0077 | 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 | g0208 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19030 | hp2 | a0006 | c0005 | t0002 | g0209 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0093 | 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 | g0084 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0066 | 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 | g0040 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ASW | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | ASW | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0029 | 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 | g0108 | AFR | LWK | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0092 | REF | REF | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0202 | REF | REF | RXFP1_chr4_158516882_158658372 | RXFP1 | chr4 | 158516882 | 158658372 |
| 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 |
| 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 |
|---|
| 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 | a0001c0001t0002a0006c0005t0002 | 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 |
| 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 | a0001c0001t0001g0002a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(155): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.49+207G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158522232 | ||||||
| chr4:158522291
|
T | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(155): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 42 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0162others(39): 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 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0004g0206others(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 | a0001c0001t0001g0027a0001c0001t0001g0115a0001c0001t0001g0116others(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 | a0001c0001t0001g0027a0001c0001t0001g0115a0001c0001t0001g0116others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0003g0029 | 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 | 99 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(96): 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 | 74 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(71): 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 | 40 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0038others(37): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): 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 | a0001c0001t0001g0105a0001c0001t0001g0200 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004others(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 | a0001c0001t0001g0201a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): 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 | a0001c0001t0001g0201a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0201a0001c0001t0001g0205a0001c0001t0004g0206others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0204others(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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0002g0113a0001c0001t0002g0181 | 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 | a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0005 | 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 | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): 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 | a0001c0001t0001g0157 | 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 | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(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 | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0103a0001c0001t0001g0151a0001c0001t0001g0152 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0009a0001c0001t0001g0040a0001c0001t0001g0041 | 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 | a0001c0001t0001g0042a0001c0001t0001g0043 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111others(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 | a0001c0001t0001g0072a0001c0001t0001g0073 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 |
9 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0076others(6): 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 | a0001c0001t0001g0208a0006c0005t0002g0209 | 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 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0102 | 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 |
32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0092others(29): Show | 33 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(30): 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 | a0001c0001t0001g0027a0001c0001t0001g0091a0001c0001t0001g0093others(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 | a0001c0001t0001g0130 | 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 | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0030a0001c0001t0001g0103a0001c0001t0001g0106others(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 | a0001c0001t0003g0034 | 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 | a0004c0006t0001g0074 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0070a0001c0001t0001g0071 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): 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 | a0001c0001t0002g0107 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0116 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | 21 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0066others(18): Show | 21 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(18): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0003c0003t0001g0003a0003c0003t0001g0004a0006c0005t0002g0209 | 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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 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 | a0006c0005t0002g0209 | 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 | a0001c0001t0001g0042a0001c0001t0001g0043 | 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 | a0001c0001t0001g0006 | 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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0002g0031 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.49+8785C>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158530810 | ||||||
| chr4:158530966
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): 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 | a0001c0001t0001g0170 | 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 | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): 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 | a0001c0001t0002g0113a0001c0001t0002g0181 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0198others(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 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0038others(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 | a0001c0001t0001g0124a0001c0001t0001g0131a0001c0001t0001g0132others(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 | 105 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0069 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0067a0001c0001t0001g0197a0001c0001t0001g0198others(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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): 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 | a0002c0002t0001g0099a0002c0002t0001g0100a0002c0002t0001g0101 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.49+14350T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158536375 | ||||||
| chr4:158536435
|
G | A | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | 112 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0001g0157 | 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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(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 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0095others(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 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0030others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0197others(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 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0197others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0197others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0197others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0159a0001c0001t0001g0197a0001c0001t0001g0198others(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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0159a0001c0001t0001g0197a0001c0001t0001g0198others(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 | a0001c0001t0001g0109 | 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0003c0003t0001g0003a0003c0003t0001g0004a0006c0005t0002g0209 | 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0003c0003t0001g0003a0003c0003t0001g0004a0006c0005t0002g0209 | 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 | a0006c0005t0002g0209 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | a0001c0001t0001g0201 | 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0136 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0192a0001c0001t0002g0107 | 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 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0123others(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 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(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 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(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 |
27 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0019others(24): 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 |
23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(20): Show | 23 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(20): 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 | a0001c0001t0001g0015a0001c0001t0001g0089 | 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 | a0001c0001t0001g0030a0001c0001t0001g0162a0001c0001t0002g0113others(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 | a0001c0001t0001g0158a0001c0001t0001g0166a0001c0001t0001g0200others(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 | a0001c0001t0001g0164a0001c0001t0001g0165a0003c0003t0001g0003others(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 | a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0006a0001c0001t0002g0107 | 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 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0164others(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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0010a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0005 | 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 | 16 | a0001c0001t0001g0033a0001c0001t0001g0115a0001c0001t0001g0170others(13): 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 | a0001c0001t0001g0183a0001c0001t0001g0196 | 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 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(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 | a0001c0001t0004g0160 | 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 | 106 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(103): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0183a0001c0001t0001g0196 | 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 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0125 | 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 | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0155others(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 | 17 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(14): 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 | a0001c0001t0001g0016a0001c0001t0001g0090 | 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 | a0001c0001t0005g0065 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0027 | 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 | a0002c0002t0001g0099 | 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 | a0001c0001t0001g0131a0001c0001t0001g0136 | 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 | a0002c0002t0001g0100a0002c0002t0001g0101 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0013a0001c0001t0001g0119 | 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 |
2 | a0001c0001t0001g0092a0001c0001t0001g0120 | 2 | NA20300.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0038a0001c0001t0001g0194 | 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 | a0001c0001t0001g0094a0001c0001t0001g0121a0001c0001t0001g0137 | 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 | a0001c0001t0001g0019a0001c0001t0001g0105 | 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 | a0001c0001t0001g0066a0001c0001t0001g0157 | 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 | a0001c0001t0004g0024 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0088others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0091a0001c0001t0001g0192 | 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 | a0001c0001t0001g0133a0001c0001t0001g0182 | 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 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0134others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0051a0001c0001t0001g0068 | 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 | a0001c0001t0001g0047a0001c0001t0001g0052 | 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 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0098others(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 | a0001c0001t0001g0077a0001c0001t0001g0128 | 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 | a0001c0001t0002g0113 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0001g0124others(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 | a0001c0001t0004g0206 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0049others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0188 | 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 | a0001c0001t0004g0207 | 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 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0001c0001t0001g0025a0001c0001t0001g0026 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0062others(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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0050a0001c0001t0001g0093a0001c0001t0001g0096others(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 | a0001c0001t0001g0191 | 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 | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(37): 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0083 | 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 | a0006c0005t0002g0209 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(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 | a0003c0003t0001g0003a0003c0003t0001g0004a0006c0005t0002g0209 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0002g0031 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.49+20769A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158542794 | ||||||
| chr4:158542843
|
C | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0159 | 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 | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0003c0003t0001g0003a0003c0003t0001g0004a0006c0005t0002g0209 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): 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 | a0003c0003t0001g0003a0003c0003t0001g0004a0006c0005t0002g0209 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0127a0001c0001t0001g0128 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0129 | 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 | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0108others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0119 | 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 | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0003g0028 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | 114 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): 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 | a0001c0001t0001g0130a0001c0001t0001g0155a0001c0001t0001g0195 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0130a0001c0001t0001g0155a0001c0001t0001g0195 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0102a0001c0001t0002g0181 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0042a0001c0001t0001g0043 | 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 | a0001c0001t0001g0042a0001c0001t0001g0043 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-23812T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548886 | ||||||
| chr4:158548917
|
A | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.50-23781A>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158548917 | ||||||
| chr4:158548964
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0105a0001c0001t0005g0037 | 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0003c0003t0001g0003a0003c0003t0001g0004a0006c0005t0002g0209 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0039 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.50-21344A>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551354 | ||||||
| chr4:158551410
|
C | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.50-21288C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158551410 | ||||||
| chr4:158551538
|
GATT | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0208 | 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0002g0107 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0015 | 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0046a0001c0001t0001g0087 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0047a0001c0001t0001g0061 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(178): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0020a0001c0001t0001g0021 | 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 | a0001c0001t0001g0062a0001c0001t0001g0063 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.50-12514C>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560184 | ||||||
| chr4:158560199
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.50-12499G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158560199 | ||||||
| chr4:158560309
|
G | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0004g0207 | 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 | a0001c0001t0001g0018a0001c0001t0001g0062a0001c0001t0001g0063others(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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0027others(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 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0095others(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 | 38 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(35): 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 | a0001c0001t0003g0034 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0041 | 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 | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0030others(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 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0038others(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 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0026others(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 | 44 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0039others(41): Show | 44 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(41): 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 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0057others(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 |
15 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0018others(12): 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 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0153others(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 | a0001c0001t0001g0016a0001c0001t0001g0105a0001c0001t0001g0204others(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 | a0001c0001t0001g0081a0001c0001t0001g0203a0001c0001t0005g0037 | 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 | a0001c0001t0004g0206 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | 3 | a0001c0001t0001g0070a0001c0001t0001g0092a0001c0001t0001g0199 | 3 | HG02145.hp2 NA19009.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(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 | 78 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0030others(75): 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 | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): 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 | a0001c0001t0001g0173a0001c0001t0001g0182a0001c0001t0001g0195others(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 | a0001c0001t0001g0043a0001c0001t0001g0051 | 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 | a0001c0001t0001g0106a0001c0001t0001g0132 | 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 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0003g0028 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0205 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0056a0001c0001t0001g0060 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0073a0001c0001t0001g0090 | 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 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0047a0001c0001t0001g0061 | 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 | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(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 | a0001c0001t0001g0205a0001c0001t0002g0107a0003c0003t0001g0003others(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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004others(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 | a0001c0001t0001g0163 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0108a0001c0001t0001g0110 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0013 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0187a0001c0001t0001g0189 | 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 | a0001c0001t0001g0190 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0046a0001c0001t0001g0087 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0004c0006t0001g0074 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0187 | 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0117 | 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 | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.50-2610G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158570088 | ||||||
| chr4:158570180
|
TAA | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(15): 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0095others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200others(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 | a0001c0001t0001g0119 | 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 | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.50-1059G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 1/17 | chr4 | 158571639 | ||||||
| chr4:158571760
|
G | GA | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0088 | 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 | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): 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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0093a0001c0001t0001g0096 | 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 | a0006c0005t0002g0209 | 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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | 13 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(10): 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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(110): 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 | a0002c0002t0001g0099a0002c0002t0001g0100a0002c0002t0001g0101 | 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 | a0001c0001t0001g0133 | 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 | 17 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(14): 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0056a0001c0001t0001g0060 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0105a0001c0001t0005g0037 | 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 | 126 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): 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 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0198others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0015 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0045a0001c0001t0001g0051 | 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 | a0001c0001t0001g0062a0001c0001t0001g0063 | 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 | a0001c0001t0001g0062a0001c0001t0001g0063 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0158 | 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 | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(94): 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 | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(94): 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 | ||||||
| chr4:158579456
|
G | A | 1 | a0001c0001t0001g0092 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.187+6621G>A | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158579456 | ||||||
| chr4:158579475
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0174 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0002g0031 | 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 | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(94): 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0127 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0201 | 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 | a0002c0002t0001g0100a0002c0002t0001g0101 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0054a0001c0001t0001g0119 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(110): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0136a0001c0001t0001g0194 | 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 | 8 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(5): Show | 8 | HG00140.hp1 HG01261.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-9127G>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158584274 | ||||||
| chr4:158584381
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076others(14): Show | 17 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(14): 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0140 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.188-7693A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158585708 | ||||||
| chr4:158585763
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.188-7638A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 2/17 | chr4 | 158585763 | ||||||
| chr4:158585886
|
T | C | 1 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0106a0001c0001t0001g0187a0001c0001t0001g0188others(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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0002g0107a0001c0001t0004g0160 | 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 | a0006c0005t0002g0209 | 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 | a0001c0001t0001g0086a0001c0001t0001g0127a0001c0001t0001g0128others(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 | 22 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(19): 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 | a0001c0001t0001g0124a0001c0001t0001g0131a0001c0001t0001g0132others(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 | 34 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(31): 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0025a0001c0001t0001g0108a0001c0001t0001g0109others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0161a0001c0001t0001g0162 | 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 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0124others(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 | a0001c0001t0001g0205 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0062a0001c0001t0001g0063 | 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 | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): 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 | a0001c0001t0001g0082 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0068a0001c0001t0001g0069 | 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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0025a0001c0001t0001g0108a0001c0001t0001g0109others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0093others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0050others(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 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0157others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0159 | 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 | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(111): 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0141 | 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 | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(111): 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 | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(109): 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0167a0001c0001t0001g0168 | 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 | a0001c0001t0001g0071 | 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 | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(111): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0062a0001c0001t0001g0063 | 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 | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(113): 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 | 33 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(30): 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0057a0001c0001t0001g0072 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(108): 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 | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(88): 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0187a0001c0001t0001g0189 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(13): Show | 16 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(13): 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0052a0001c0001t0001g0129 | 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 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 | a0001c0001t0001g0152a0001c0001t0001g0205a0003c0003t0001g0003others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0057a0001c0001t0001g0072a0005c0004t0001g0118 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0022 | 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 | a0001c0001t0001g0201a0001c0001t0002g0112a0001c0001t0002g0113others(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 | 18 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(15): 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 | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(96): 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0020a0001c0001t0001g0021 | 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 | a0001c0001t0001g0027a0001c0001t0001g0098a0001c0001t0001g0140others(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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0026a0001c0001t0001g0080a0001c0001t0004g0024 | 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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0103 | 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 | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(112): 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0116a0001c0001t0001g0167a0001c0001t0001g0168others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | 41 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 41 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(38): 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 | a0001c0001t0001g0030a0001c0001t0001g0082a0001c0001t0001g0174 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0094a0002c0002t0001g0099a0002c0002t0001g0100others(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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0067 | 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 | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): 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 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0117 | 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 | a0001c0001t0001g0136a0001c0001t0001g0154a0001c0001t0001g0194 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0025a0001c0001t0001g0155a0001c0001t0001g0195 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(111): 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(108): 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 | a0001c0001t0001g0208 | 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 | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(37): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0038a0001c0001t0001g0116a0001c0001t0001g0128others(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 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0059others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0048a0001c0001t0001g0049 | 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 | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(113): 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0004g0160 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0010a0001c0001t0001g0022 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0005g0065 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0005g0065 | 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 | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(111): 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 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0091 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0054 | 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 | a0001c0001t0005g0065 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0172a0001c0001t0001g0176 | 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 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0060others(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 | 40 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(37): 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0170others(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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0054others(17): 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 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0001g0125others(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 | a0001c0001t0001g0115a0001c0001t0001g0170a0001c0001t0001g0171others(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 | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(2): 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 | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): 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 | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(93): Show | 97 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(94): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0025a0001c0001t0001g0116a0001c0001t0001g0122others(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 | a0001c0001t0001g0124a0001c0001t0001g0131a0001c0001t0001g0151 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0090others(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 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0170others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0090others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0161 | 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 | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(113): 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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111others(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 | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(113): 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0192 | 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 | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(111): 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 | a0001c0001t0002g0031a0001c0001t0002g0107a0001c0001t0002g0112others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0152others(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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | a0001c0001t0001g0049 | 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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(113): 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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 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 | 30 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(27): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0073others(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 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0098others(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 | a0001c0001t0001g0045a0001c0001t0001g0051 | 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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(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 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 9 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0106others(6): 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 | a0001c0001t0001g0030a0001c0001t0001g0200 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0084 | 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 |
9 | a0001c0001t0001g0042a0001c0001t0001g0075a0001c0001t0001g0077others(6): Show | 9 | HG01123.hp2 HG01261.hp1 HG03239.hp2 others(6): 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 | a0001c0001t0001g0085a0001c0001t0001g0152 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0040a0001c0001t0001g0055a0001c0001t0001g0081others(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 | 15 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0033others(12): 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 | a0001c0001t0001g0155a0001c0001t0001g0195a0001c0001t0003g0028others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | a0001c0001t0001g0152a0001c0001t0001g0205a0003c0003t0001g0003others(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 | a0001c0001t0001g0009 | 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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | a0001c0001t0001g0201 | 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 | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(92): 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200 | 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 | a0001c0001t0002g0031a0001c0001t0004g0160 | 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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | a0001c0001t0004g0160 | 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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): 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 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0067 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0006c0005t0002g0209 | 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 | a0001c0001t0001g0030a0001c0001t0001g0159a0001c0001t0001g0170others(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 | a0001c0001t0001g0050a0001c0001t0001g0106a0001c0001t0001g0122others(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 | 11 | a0001c0001t0001g0152a0001c0001t0001g0171a0001c0001t0001g0172others(8): 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 | a0001c0001t0001g0115a0001c0001t0001g0157a0001c0001t0001g0174 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0040a0001c0001t0001g0055a0001c0001t0001g0058others(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 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(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 | 19 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0019others(16): Show | 19 | HG00099.hp1 HG00738.hp1 HG01099.hp1 others(16): 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 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0041others(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 | a0001c0001t0001g0018a0001c0001t0001g0071a0001c0001t0001g0085others(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 | a0001c0001t0001g0079a0001c0001t0001g0090 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0137a0001c0001t0001g0156a0001c0001t0002g0181 | 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 | a0001c0001t0001g0143a0001c0001t0002g0113 | 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 | a0001c0001t0001g0096a0001c0001t0001g0146a0001c0001t0002g0112others(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 | a0001c0001t0001g0093a0001c0001t0001g0144a0001c0001t0001g0145 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0008a0001c0001t0001g0109a0001c0001t0001g0158 | 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 | a0001c0001t0001g0073a0001c0001t0001g0103a0001c0001t0001g0116others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0110others(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 | a0001c0001t0001g0025a0001c0001t0001g0094a0001c0001t0001g0097others(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 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0108others(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 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0095others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0127others(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 | 34 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(31): 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 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0048others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(12): 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 | 34 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(31): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0173a0001c0001t0003g0028a0001c0001t0003g0034others(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 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0106others(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 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0174others(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 | a0001c0001t0001g0115a0001c0001t0001g0170a0001c0001t0001g0172others(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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0042others(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 | 55 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(52): 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 | 50 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0038others(47): Show | 51 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(48): 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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0130others(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 | a0001c0001t0001g0187a0001c0001t0001g0189 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0060others(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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0025a0001c0001t0001g0155a0001c0001t0001g0195 | 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0151 | 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 | a0001c0001t0001g0110a0001c0001t0001g0124a0001c0001t0001g0132 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0137a0001c0001t0001g0139a0002c0002t0001g0101 | 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 | a0002c0002t0001g0100 | 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 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0125 | 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 | a0001c0001t0001g0108a0001c0001t0001g0116a0001c0001t0001g0167others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0123a0001c0001t0001g0127a0001c0001t0001g0195 | 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 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(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 | a0001c0001t0001g0027a0001c0001t0001g0098a0001c0001t0001g0128others(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 | a0001c0001t0001g0102a0001c0001t0001g0122a0002c0002t0001g0099 | 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 | a0001c0001t0001g0103a0001c0001t0001g0154 | 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 | a0001c0001t0001g0025a0001c0001t0001g0073a0001c0001t0001g0094others(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 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0130 | 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 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0194 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0093a0001c0001t0001g0096 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0090others(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 | a0001c0001t0001g0025a0001c0001t0001g0108a0001c0001t0001g0109others(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 | a0001c0001t0005g0065 | 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 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0106a0001c0001t0001g0159a0001c0001t0001g0161others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(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 | a0001c0001t0001g0115a0001c0001t0001g0174 | 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 | a0001c0001t0001g0016 | 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 | 37 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0106others(34): 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 | a0001c0001t0001g0201 | 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 | 36 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0106others(33): 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 | 36 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0106others(33): 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 | 36 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0106others(33): 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 | ||||||
| chr4:158631483
|
A | G | 1 | a0001c0001t0001g0092 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.900-1922A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 11/17 | chr4 | 158631483 | ||||||
| chr4:158631956
|
G | T | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0144a0001c0001t0001g0145 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0021a0001c0001t0001g0153 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0009 | 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 | a0002c0002t0001g0099 | 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 | a0001c0001t0004g0160a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 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 | a0001c0001t0001g0152 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0061 | 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 | 44 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(41): 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | 44 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(41): 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0004g0160 | 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 | 49 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(46): 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 | 41 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(38): 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 | a0001c0001t0001g0155a0001c0001t0001g0195 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0124others(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 | a0001c0001t0001g0023 | 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 | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(104): 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 | a0001c0001t0001g0152 | 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 | 44 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(41): 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 | a0001c0001t0001g0167a0001c0001t0001g0168 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0001g0039a0001c0001t0001g0070a0001c0001t0001g0071 | 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 | a0001c0001t0004g0160 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0150 | 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 | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(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 | a0001c0001t0004g0160a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0009a0001c0001t0001g0013 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0075 | 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 | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0002g0031a0001c0001t0002g0107a0001c0001t0002g0112others(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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0002g0031a0001c0001t0002g0107a0001c0001t0002g0112others(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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0157a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0017a0001c0001t0001g0060 | 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 | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(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 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0035others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0004g0160a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0073a0001c0001t0001g0137a0001c0001t0001g0138others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0062a0001c0001t0001g0063 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0022others(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 | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0115others(16): 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(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 | 83 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): 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 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0042others(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 | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1116-1407T>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643502 | ||||||
| chr4:158643531
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1116-1378T>C | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158643531 | ||||||
| chr4:158643574
|
C | T | 8 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(5): Show | 8 | HG00140.hp1 HG01261.hp1 HG02257.hp1 others(5): 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0125 | 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 | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0042a0001c0001t0001g0043 | 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 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0161others(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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0200others(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 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0125others(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 | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): 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 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0087others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(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 | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1116-777C>T | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 14/17 | chr4 | 158644132 | ||||||
| chr4:158644147
|
C | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): 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 | a0001c0001t0001g0138a0001c0001t0001g0141 | 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 | a0001c0001t0001g0088 | 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 | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): 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 | a0001c0001t0001g0093a0001c0001t0001g0096 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | a0001c0001t0004g0024a0001c0001t0004g0206a0001c0001t0004g0207 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(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 | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0004g0024a0001c0001t0004g0160a0001c0001t0004g0206others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0012 | 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 | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0152 | 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 | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1756+30A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 16/17 | chr4 | 158647231 | ||||||
| chr4:158647508
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): 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 | a0001c0001t0001g0075a0001c0001t0001g0076 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0004g0024a0001c0001t0004g0160a0001c0001t0004g0206others(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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | ||||||
| chr4:158649627
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1975+910A>G | RXFP1 | ENSG00000171509.16 | transcript | ENST00000307765.10 | protein_coding | 17/17 | chr4 | 158649627 | ||||||
| chr4:158649678
|
T | TA | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0127a0001c0001t0001g0128 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0152 | 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 | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097 | 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 | a0001c0001t0001g0201 | 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 | 24 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0040others(21): 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 | AATATAT | 39 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0038others(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 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0110others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(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 | a0001c0001t0001g0025a0001c0001t0001g0116a0001c0001t0001g0169others(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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0130a0001c0001t0001g0168 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0159others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0205a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0130 | 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 | a0001c0001t0001g0201 | 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 | a0003c0003t0001g0003a0003c0003t0001g0004 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 |