| geneid | 122042 |
|---|---|
| ensemblid | ENSG00000133105.8 |
| hgncid | 17318 |
| symbol | RXFP2 |
| name | relaxin family peptide receptor 2 |
| refseq_nuc | NM_130806.5 |
| refseq_prot | NP_570718.1 |
| ensembl_nuc | ENST00000298386.7 |
| ensembl_prot | ENSP00000298386.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 31739526 |
| end | 31803389 |
| strand | + |
| ver | v1.2 |
| region | chr13:31739526-31803389 |
| region5000 | chr13:31734526-31808389 |
| regionname0 | RXFP2_chr13_31739526_31803389 |
| regionname5000 | RXFP2_chr13_31734526_31808389 |
| 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 | 754 | 325 | 81 | 48 | 152 | 6 | 36 | 125 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0002 | 0/0 | 754 | 52 | 6 | 8 | 36 | 2 | 0 | 27 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0003 | 0/0 | 754 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0004 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0005 | 0/0 | 754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0006 | 0/0 | 754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0007 | 0/0 | 754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0008 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0009 | 0/0 | 754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| 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 | 0/1 | 2265 | 173 | 41 | 27 | 82 | 2 | 20 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0002 | 1/0 | 2265 | 126 | 38 | 20 | 50 | 2 | 15 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0003 | 0/0 | 2265 | 51 | 5 | 8 | 36 | 2 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0004 | 0/0 | 2265 | 23 | 0 | 0 | 20 | 2 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0005 | 0/0 | 2265 | 3 | 3 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0006 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0007 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0008 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0009 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0010 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0011 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0012 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0013 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0014 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| c0015 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| 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 | 0/1 | 1072 | 176 | 21 | 29 | 98 | 4 | 23 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| t0002 | 1/0 | 1072 | 143 | 57 | 20 | 50 | 2 | 13 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| t0003 | 0/0 | 1072 | 55 | 7 | 9 | 37 | 2 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| t0004 | 0/0 | 1072 | 5 | 5 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| t0005 | 0/0 | 1072 | 3 | 0 | 0 | 3 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| t0006 | 0/0 | 1072 | 2 | 0 | 0 | 0 | 0 | 2 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| t0007 | 0/0 | 1072 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| t0008 | 0/0 | 1072 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| 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 | 1 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| 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 | 0/1 | 2265 | 173 | 41 | 27 | 82 | 2 | 20 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0002 | 1/0 | 2265 | 126 | 38 | 20 | 50 | 2 | 15 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0004 | 0/0 | 2265 | 23 | 0 | 0 | 20 | 2 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0011 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0013 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0015 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0002c0003 | 0/0 | 2265 | 51 | 5 | 8 | 36 | 2 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0002c0012 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0003c0005 | 0/0 | 2265 | 3 | 3 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0004c0014 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0005c0009 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0006c0010 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0007c0008 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0008c0007 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0009c0006 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3336 | 147 | 20 | 26 | 78 | 2 | 20 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0001t0002 | 0/0 | 3336 | 15 | 14 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0001t0003 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0001t0004 | 0/0 | 3336 | 5 | 5 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0001t0005 | 0/0 | 3336 | 3 | 0 | 0 | 3 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0001t0008 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0002t0001 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0002t0002 | 1/0 | 3336 | 122 | 38 | 19 | 49 | 2 | 13 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0002t0006 | 0/0 | 3336 | 2 | 0 | 0 | 0 | 0 | 2 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0002t0007 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0004t0001 | 0/0 | 3336 | 23 | 0 | 0 | 20 | 2 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0011t0001 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0013t0002 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0001c0015t0003 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0002c0003t0003 | 0/0 | 3336 | 51 | 5 | 8 | 36 | 2 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0002c0012t0002 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0003c0005t0002 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0004c0014t0002 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0005c0009t0001 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0006c0010t0001 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0007c0008t0001 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0008c0007t0003 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| a0009c0006t0001 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | copy fasta | chr13 | 31734526 | 31808389 |
| 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 | 1 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0006g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0006g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0007g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0011t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0013t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0015t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0012t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0003c0005t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0003c0005t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0003c0005t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0004c0014t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0005c0009t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0006c0010t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0007c0008t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0008c0007t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0009c0006t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0297 | EUR | GBR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | FIN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0135 | EUR | FIN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00438 | hp1 | a0002 | c0003 | t0003 | g0085 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0334 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00609 | hp1 | a0002 | c0003 | t0003 | g0052 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0283 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0383 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0335 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00673 | hp2 | a0002 | c0003 | t0003 | g0057 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0075 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0304 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01071 | hp2 | a0009 | c0006 | t0001 | g0258 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0360 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01074 | hp2 | a0002 | c0003 | t0003 | g0104 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0327 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0313 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0378 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01167 | hp1 | a0002 | c0003 | t0003 | g0074 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0373 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0361 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01243 | hp1 | a0001 | c0015 | t0003 | g0376 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0299 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0310 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0359 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0306 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01346 | hp2 | a0007 | c0008 | t0001 | g0081 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0320 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0315 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01433 | hp2 | a0002 | c0003 | t0003 | g0029 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0255 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01515 | hp1 | a0002 | c0003 | t0003 | g0037 | EUR | IBS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0300 | EUR | IBS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0350 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0298 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0322 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02004 | hp2 | a0002 | c0003 | t0003 | g0068 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02015 | hp1 | a0002 | c0003 | t0003 | g0133 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0049 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0095 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0333 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02074 | hp1 | a0002 | c0003 | t0003 | g0071 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0330 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0374 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0319 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02132 | hp2 | a0001 | c0004 | t0001 | g0281 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0340 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02148 | hp2 | a0002 | c0003 | t0003 | g0058 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02155 | hp1 | a0002 | c0003 | t0003 | g0051 | EAS | CDX | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0280 | EAS | CDX | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0251 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02273 | hp2 | a0002 | c0003 | t0003 | g0062 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0365 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0336 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0253 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02451 | hp2 | a0001 | c0013 | t0002 | g0012 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02572 | hp2 | a0002 | c0003 | t0003 | g0090 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0369 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0250 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02647 | hp1 | a0002 | c0003 | t0003 | g0091 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0285 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0316 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0273 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02735 | hp1 | a0005 | c0009 | t0001 | g0174 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0302 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0153 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02886 | hp1 | a0003 | c0005 | t0002 | g0242 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0382 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0381 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0146 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02976 | hp1 | a0002 | c0003 | t0003 | g0028 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0368 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0249 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03130 | hp1 | a0002 | c0012 | t0002 | g0124 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0377 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0379 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03209 | hp1 | a0003 | c0005 | t0002 | g0241 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0364 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0166 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0229 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03453 | hp2 | a0003 | c0005 | t0002 | g0105 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0286 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0156 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03688 | hp1 | a0006 | c0010 | t0001 | g0047 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0326 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03704 | hp1 | a0001 | c0002 | t0006 | g0314 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0357 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0288 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03927 | hp1 | a0001 | c0002 | t0006 | g0338 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0339 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0308 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0323 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0138 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0363 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0252 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | CHB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0023 | EAS | CHB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0354 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18942 | hp2 | a0002 | c0003 | t0003 | g0066 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0217 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18946 | hp2 | a0002 | c0003 | t0003 | g0063 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18948 | hp1 | a0002 | c0003 | t0003 | g0059 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18949 | hp1 | a0002 | c0003 | t0003 | g0083 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0126 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18951 | hp2 | a0002 | c0003 | t0003 | g0053 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18952 | hp2 | a0002 | c0003 | t0003 | g0056 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18954 | hp2 | a0002 | c0003 | t0003 | g0067 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18956 | hp1 | a0002 | c0003 | t0003 | g0060 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18959 | hp1 | a0002 | c0003 | t0003 | g0065 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18959 | hp2 | a0001 | c0004 | t0001 | g0076 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0341 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18964 | hp2 | a0008 | c0007 | t0003 | g0061 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18966 | hp1 | a0002 | c0003 | t0003 | g0054 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0347 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0346 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18968 | hp1 | a0002 | c0003 | t0003 | g0048 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18970 | hp1 | a0002 | c0003 | t0003 | g0287 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0127 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18974 | hp1 | a0001 | c0004 | t0001 | g0084 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18978 | hp2 | a0002 | c0003 | t0003 | g0050 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0380 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0082 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18981 | hp1 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18983 | hp1 | a0001 | c0004 | t0001 | g0128 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0345 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18987 | hp1 | a0002 | c0003 | t0003 | g0370 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18988 | hp2 | a0001 | c0002 | t0007 | g0329 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0362 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18990 | hp1 | a0001 | c0004 | t0001 | g0020 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18994 | hp1 | a0002 | c0003 | t0003 | g0072 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0343 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0129 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19001 | hp1 | a0002 | c0003 | t0003 | g0064 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19002 | hp2 | a0001 | c0004 | t0001 | g0077 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19003 | hp1 | a0004 | c0014 | t0002 | g0305 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0021 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19005 | hp2 | a0001 | c0004 | t0001 | g0132 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0080 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19009 | hp2 | a0002 | c0003 | t0003 | g0234 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19011 | hp1 | a0002 | c0003 | t0003 | g0223 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19012 | hp1 | a0002 | c0003 | t0003 | g0233 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0318 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0356 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19064 | hp1 | a0002 | c0003 | t0003 | g0073 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19065 | hp1 | a0002 | c0003 | t0003 | g0371 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0282 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0078 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19074 | hp1 | a0001 | c0004 | t0001 | g0130 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0344 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19080 | hp1 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19081 | hp1 | a0002 | c0003 | t0003 | g0094 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0293 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0352 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19083 | hp2 | a0002 | c0003 | t0003 | g0070 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19084 | hp1 | a0001 | c0004 | t0001 | g0079 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19086 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0348 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19091 | hp2 | a0002 | c0003 | t0003 | g0069 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0158 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0089 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | ASW | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ASW | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20752 | hp1 | a0002 | c0003 | t0003 | g0102 | EUR | TSI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20752 | hp2 | a0001 | c0004 | t0001 | g0134 | EUR | TSI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0284 | SAS | GIH | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | GIH | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02109 | hp1 | a0001 | c0011 | t0001 | g0254 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0225 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | USA | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0366 | AFR | USA | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | USA | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | USA | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0375 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0192 | REF | REF | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0097 | REF | REF | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31758347
|
G | A | 1 | a0009 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.184G>A | p.Ala62Thr | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/18 | 271/3336 | 184/2265 | 62/754 | chr13 | 31758347 | ||
| chr13:31758383
|
G | A | 1 | a0008 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.220G>A | p.Gly74Arg | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/18 | 307/3336 | 220/2265 | 74/754 | chr13 | 31758383 | ||
| chr13:31777423
|
C | T | 1 | a0004 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.689C>T | p.Thr230Met | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 8/18 | 776/3336 | 689/2265 | 230/754 | chr13 | 31777423 | ||
| chr13:31781678
|
G | A | 1 | a0007 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.793G>A | p.Glu265Lys | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 10/18 | 880/3336 | 793/2265 | 265/754 | chr13 | 31781678 | ||
| chr13:31786624
|
C | A | 1 | a0005 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1060C>A | p.Gln354Lys | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/18 | 1147/3336 | 1060/2265 | 354/754 | chr13 | 31786624 | ||
| chr13:31792908
|
C | T | 1 | a0003 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1606C>T | p.Arg536Trp | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/18 | 1693/3336 | 1606/2265 | 536/754 | chr13 | 31792908 | ||
| chr13:31792924
|
T | C | 1 | a0006 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1622T>C | p.Ile541Thr | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/18 | 1709/3336 | 1622/2265 | 541/754 | chr13 | 31792924 | ||
| chr13:31797224
|
A | G | 2 | a0002a0008 | 53 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(50): Show |
missense_variant | MODERATE | c.1810A>G | p.Ile604Val | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/18 | 1897/3336 | 1810/2265 | 604/754 | chr13 | 31797224 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31761743
|
G | A | 2 | a0001c0004a0007c0008 | 24 | HG00280.hp2 HG00621.hp1 HG01346.hp2 others(21): Show |
synonymous_variant | LOW | c.261G>A | p.Ala87Ala | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/18 | 348/3336 | 261/2265 | 87/754 | chr13 | 31761743 | ||
| chr13:31761779
|
C | T | 1 | a0001c0015 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.297C>T | p.Ser99Ser | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/18 | 384/3336 | 297/2265 | 99/754 | chr13 | 31761779 | ||
| chr13:31786410
|
A | G | 13 | a0001c0001a0001c0004a0001c0011others(10): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
synonymous_variant | LOW | c.957A>G | p.Glu319Glu | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 12/18 | 1044/3336 | 957/2265 | 319/754 | chr13 | 31786410 | ||
| chr13:31786446
|
A | G | 3 | a0001c0013a0002c0003a0008c0007 | 53 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(50): Show |
synonymous_variant | LOW | c.993A>G | p.Leu331Leu | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 12/18 | 1080/3336 | 993/2265 | 331/754 | chr13 | 31786446 | ||
| chr13:31802372
|
A | G | 1 | a0001c0011 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.2232A>G | p.Thr744Thr | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 18/18 | 2319/3336 | 2232/2265 | 744/754 | chr13 | 31802372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31802581
|
A | G | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(11): Show | 235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*176A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 18/18 | 176 | chr13 | 31802581 | |||||
| chr13:31802646
|
G | A | 1 | a0001c0002t0006 | 2 | HG03704.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*241G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 18/18 | 241 | chr13 | 31802646 | |||||
| chr13:31802802
|
C | T | 1 | a0001c0001t0004 | 5 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*397C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 18/18 | 397 | chr13 | 31802802 | |||||
| chr13:31802925
|
G | A | 1 | a0001c0001t0008 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*520G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 18/18 | 520 | chr13 | 31802925 | |||||
| chr13:31802991
|
G | C | 4 | a0001c0001t0003a0001c0015t0003a0002c0003t0003others(1): Show | 55 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*586G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 18/18 | 586 | chr13 | 31802991 | |||||
| chr13:31803253
|
T | C | 1 | a0001c0001t0005 | 3 | NA19000.hp1 NA19010.hp2 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*848T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 18/18 | 848 | chr13 | 31803253 | |||||
| chr13:31803330
|
G | A | 1 | a0001c0002t0007 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*925G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 18/18 | 925 | chr13 | 31803330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31739756
|
C | T | 1 | a0001c0002t0002g0383 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.94+50C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31739756 | ||||||
| chr13:31739804
|
TA | T | 9 | a0001c0002t0002g0375a0001c0002t0002g0379a0001c0002t0002g0380others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+108delA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31739804 | |||||
| chr13:31739854
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.94+148T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31739854 | ||||||
| chr13:31739861
|
T | C | 1 | a0001c0002t0002g0005 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.94+155T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31739861 | ||||||
| chr13:31739892
|
C | T | 1 | a0001c0002t0002g0373 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.94+186C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31739892 | ||||||
| chr13:31740075
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0256a0001c0001t0001g0257others(133): Show | 138 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.94+369C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31740075 | ||||||
| chr13:31740753
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0256a0001c0001t0001g0257others(133): Show | 138 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.94+1047G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31740753 | ||||||
| chr13:31740913
|
A | G | 2 | a0001c0002t0002g0381a0001c0002t0002g0382 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.94+1207A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31740913 | ||||||
| chr13:31741050
|
A | C | 1 | a0001c0001t0001g0248 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.94+1344A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741050 | ||||||
| chr13:31741171
|
C | A | 5 | a0001c0002t0002g0249a0001c0002t0002g0250a0001c0002t0002g0251others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1465C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741171 | ||||||
| chr13:31741179
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0106a0001c0001t0001g0107others(144): Show | 148 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.94+1473A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741179 | ||||||
| chr13:31741213
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0256a0001c0001t0001g0257others(133): Show | 138 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.94+1507A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741213 | ||||||
| chr13:31741269
|
T | C | 6 | a0001c0002t0002g0375a0001c0002t0002g0379a0001c0011t0001g0254others(3): Show | 6 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1563T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741269 | ||||||
| chr13:31741356
|
T | C | 13 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(10): Show | 13 | NA18950.hp1 NA18968.hp2 NA18973.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+1650T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741356 | ||||||
| chr13:31741427
|
C | G | 1 | a0003c0005t0002g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.94+1721C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741427 | ||||||
| chr13:31741445
|
T | C | 7 | a0001c0001t0002g0004a0001c0001t0002g0120a0001c0001t0002g0121others(4): Show | 7 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1739T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741445 | ||||||
| chr13:31741578
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0103a0002c0003t0003g0102others(1): Show | 4 | HG01074.hp2 HG02683.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1872C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741578 | ||||||
| chr13:31741664
|
G | A | 13 | a0001c0001t0001g0125a0001c0002t0002g0136a0001c0004t0001g0126others(10): Show | 13 | HG00280.hp2 HG02015.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+1958G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741664 | ||||||
| chr13:31741761
|
G | A | 1 | a0001c0002t0002g0255 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.94+2055G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741761 | ||||||
| chr13:31741993
|
G | C | 3 | a0001c0002t0002g0380a0001c0002t0002g0381a0001c0002t0002g0382 | 3 | HG02895.hp2 HG02897.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.94+2287G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31741993 | ||||||
| chr13:31742223
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94+2517G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31742223 | ||||||
| chr13:31742293
|
C | T | 3 | a0001c0001t0002g0100a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | HG02717.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.94+2587C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31742293 | ||||||
| chr13:31742642
|
A | AT | 12 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | NA18950.hp1 NA18968.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+2937dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31742642 | |||||
| chr13:31742742
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(297): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.94+3036G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31742742 | ||||||
| chr13:31742801
|
G | A | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(376): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.94+3095G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31742801 | ||||||
| chr13:31742840
|
A | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(284): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.94+3134A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31742840 | ||||||
| chr13:31742880
|
C | CA | 128 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(125): Show | 129 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.94+3175dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31742880 | |||||
| chr13:31743112
|
C | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0107others(127): Show | 131 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.94+3406C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743112 | ||||||
| chr13:31743112
|
C | T | 1 | a0001c0001t0004g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.94+3406C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743112 | ||||||
| chr13:31743197
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.94+3491A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743197 | ||||||
| chr13:31743214
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+3508C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743214 | ||||||
| chr13:31743246
|
A | G | 127 | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0001g0276others(124): Show | 128 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.94+3540A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743246 | ||||||
| chr13:31743352
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.94+3646C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743352 | ||||||
| chr13:31743360
|
C | T | 2 | a0002c0003t0003g0370a0002c0003t0003g0371 | 2 | NA18987.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.94+3654C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743360 | ||||||
| chr13:31743402
|
A | G | 1 | a0002c0003t0003g0094 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.94+3696A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743402 | ||||||
| chr13:31743447
|
G | A | 10 | a0001c0001t0001g0271a0001c0002t0002g0249a0001c0002t0002g0250others(7): Show | 10 | HG01175.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+3741G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743447 | ||||||
| chr13:31743473
|
TA | T | 204 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(201): Show | 205 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.94+3780delA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31743473 | |||||
| chr13:31743499
|
G | C | 14 | a0001c0001t0001g0125a0001c0002t0002g0136a0001c0004t0001g0126others(11): Show | 14 | HG00280.hp2 HG02015.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+3793G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743499 | ||||||
| chr13:31743502
|
T | C | 1 | a0001c0001t0004g0243 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+3796T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743502 | ||||||
| chr13:31743569
|
A | G | 1 | a0001c0001t0002g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+3863A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743569 | ||||||
| chr13:31743692
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0002g0239 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.94+3986A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743692 | ||||||
| chr13:31743806
|
T | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 130 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.94+4100T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743806 | ||||||
| chr13:31743891
|
A | C | 7 | a0001c0001t0001g0367a0001c0002t0002g0363a0001c0002t0002g0364others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+4185A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743891 | ||||||
| chr13:31743922
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | NA18960.hp2 NA18963.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.94+4216A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743922 | ||||||
| chr13:31743964
|
A | C | 243 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(240): Show | 244 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.94+4258A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31743964 | ||||||
| chr13:31744017
|
C | T | 3 | a0001c0001t0001g0367a0001c0002t0002g0368a0001c0002t0002g0369 | 3 | HG02559.hp2 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.94+4311C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744017 | ||||||
| chr13:31744038
|
G | A | 3 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0001t0004g0238 | 3 | HG02965.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.94+4332G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744038 | ||||||
| chr13:31744236
|
T | C | 116 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.94+4530T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744236 | ||||||
| chr13:31744240
|
A | G | 8 | a0001c0001t0001g0019a0001c0001t0002g0017a0001c0001t0002g0018others(5): Show | 8 | HG01496.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+4534A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744240 | ||||||
| chr13:31744280
|
C | G | 116 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.94+4574C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744280 | ||||||
| chr13:31744305
|
T | C | 2 | a0001c0002t0002g0381a0001c0002t0002g0382 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.94+4599T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744305 | ||||||
| chr13:31744421
|
A | G | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.94+4715A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744421 | ||||||
| chr13:31744505
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | NA18947.hp1 NA18967.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.94+4799G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744505 | ||||||
| chr13:31744594
|
A | G | 1 | a0001c0001t0004g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.94+4888A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744594 | ||||||
| chr13:31744658
|
A | T | 1 | a0002c0003t0003g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.94+4952A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744658 | ||||||
| chr13:31744693
|
C | A | 6 | a0001c0001t0001g0019a0001c0001t0002g0017a0001c0001t0002g0018others(3): Show | 6 | HG01496.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+4987C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744693 | ||||||
| chr13:31744718
|
G | GT | 111 | a0001c0001t0001g0137a0001c0001t0001g0289a0001c0001t0001g0290others(108): Show | 112 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.94+5022dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31744718 | |||||
| chr13:31744722
|
T | TC | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(123): Show | 128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.94+5016_94+5017ins others(1): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744722 | ||||||
| chr13:31744780
|
G | A | 1 | a0002c0003t0003g0094 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.94+5074G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744780 | ||||||
| chr13:31744815
|
G | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 28 | HG00621.hp1 HG01243.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+5109G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744815 | ||||||
| chr13:31744886
|
C | T | 1 | a0001c0002t0002g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94+5180C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744886 | ||||||
| chr13:31744887
|
A | G | 378 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(375): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.94+5181A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744887 | ||||||
| chr13:31744894
|
C | T | 94 | a0001c0001t0001g0137a0001c0001t0001g0289a0001c0001t0001g0290others(91): Show | 95 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.94+5188C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744894 | ||||||
| chr13:31744942
|
G | A | 2 | a0001c0002t0002g0373a0001c0011t0001g0254 | 2 | HG01175.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.94+5236G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744942 | ||||||
| chr13:31744985
|
A | G | 1 | a0001c0002t0002g0362 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.94+5279A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744985 | ||||||
| chr13:31744987
|
G | A | 4 | a0001c0002t0002g0379a0001c0015t0003g0376a0002c0003t0003g0377others(1): Show | 4 | HG01106.hp2 HG01243.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+5281G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31744987 | ||||||
| chr13:31745031
|
G | A | 12 | a0001c0001t0002g0004a0001c0001t0002g0100a0001c0001t0002g0120others(9): Show | 12 | HG02109.hp2 HG02486.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+5325G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745031 | ||||||
| chr13:31745040
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.94+5334C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745040 | ||||||
| chr13:31745181
|
AG | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0120a0001c0001t0002g0121others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+5476delG | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745181 | ||||||
| chr13:31745207
|
G | T | 1 | a0001c0002t0002g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.94+5501G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745207 | ||||||
| chr13:31745228
|
C | G | 3 | a0001c0002t0002g0359a0001c0002t0002g0360a0001c0002t0002g0361 | 3 | HG01074.hp1 HG01192.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.94+5522C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745228 | ||||||
| chr13:31745366
|
A | T | 140 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(137): Show | 140 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.94+5660A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745366 | ||||||
| chr13:31745450
|
A | G | 6 | a0001c0001t0001g0019a0001c0001t0002g0017a0001c0001t0002g0018others(3): Show | 6 | HG01496.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5744A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745450 | ||||||
| chr13:31745743
|
G | A | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 235 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(232): Show |
intron_variant | MODIFIER | c.94+6037G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745743 | ||||||
| chr13:31745857
|
T | C | 134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(131): Show | 134 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.94+6151T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745857 | ||||||
| chr13:31745914
|
C | T | 46 | a0001c0001t0001g0046a0001c0001t0001g0106a0001c0002t0002g0055others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.94+6208C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745914 | ||||||
| chr13:31745915
|
A | G | 134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(131): Show | 134 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.94+6209A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745915 | ||||||
| chr13:31745939
|
G | A | 134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(131): Show | 134 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.94+6233G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31745939 | ||||||
| chr13:31746107
|
G | A | 2 | a0001c0002t0002g0368a0001c0002t0002g0369 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.94+6401G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746107 | ||||||
| chr13:31746157
|
A | G | 9 | a0001c0004t0001g0076a0001c0004t0001g0077a0001c0004t0001g0078others(6): Show | 9 | HG01346.hp2 NA18949.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+6451A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746157 | ||||||
| chr13:31746579
|
A | G | 99 | a0001c0001t0001g0137a0001c0001t0001g0289a0001c0001t0001g0290others(96): Show | 100 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.94+6873A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746579 | ||||||
| chr13:31746686
|
T | C | 3 | a0001c0001t0001g0256a0001c0001t0001g0257a0009c0006t0001g0258 | 3 | HG01071.hp2 HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.94+6980T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746686 | ||||||
| chr13:31746763
|
A | T | 135 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(132): Show | 135 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.94+7057A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746763 | ||||||
| chr13:31746765
|
A | T | 134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(131): Show | 134 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.94+7059A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746765 | ||||||
| chr13:31746767
|
T | TATTATAT others(24): Show |
134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(131): Show | 134 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.94+7062_94+7063ins others(31): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31746767 | |||||
| chr13:31746767
|
T | TTATATAC others(22): Show |
1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94+7061_94+7062ins others(29): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746767 | ||||||
| chr13:31746795
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.94+7089A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746795 | ||||||
| chr13:31746812
|
A | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0002c0012t0002g0124 | 3 | HG02922.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.94+7106A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746812 | ||||||
| chr13:31746972
|
T | A | 17 | a0001c0001t0001g0271a0001c0001t0001g0367a0001c0001t0001g0372others(14): Show | 17 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+7266T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31746972 | ||||||
| chr13:31747224
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0002g0025a0001c0001t0002g0026others(2): Show | 5 | HG02717.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7518G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31747224 | ||||||
| chr13:31747241
|
G | A | 1 | a0001c0002t0002g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.94+7535G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31747241 | ||||||
| chr13:31747333
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.94+7627A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31747333 | ||||||
| chr13:31747386
|
G | A | 1 | a0002c0003t0003g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94+7680G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31747386 | ||||||
| chr13:31747484
|
G | T | 1 | a0001c0001t0002g0230 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.94+7778G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31747484 | ||||||
| chr13:31747593
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.94+7887C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31747593 | ||||||
| chr13:31747787
|
T | A | 96 | a0001c0001t0001g0137a0001c0001t0001g0289a0001c0001t0001g0290others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.94+8081T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31747787 | ||||||
| chr13:31747911
|
G | A | 4 | a0001c0002t0002g0136a0001c0002t0002g0380a0001c0002t0002g0381others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+8205G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31747911 | ||||||
| chr13:31748122
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.94+8416C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748122 | ||||||
| chr13:31748123
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.94+8417G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748123 | ||||||
| chr13:31748304
|
T | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0239 | 3 | HG02922.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.94+8598T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748304 | ||||||
| chr13:31748577
|
G | A | 1 | a0001c0002t0002g0270 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.94+8871G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748577 | ||||||
| chr13:31748643
|
T | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0151 | 2 | NA18612.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.94+8937T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748643 | ||||||
| chr13:31748672
|
C | T | 1 | a0001c0004t0001g0084 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.94+8966C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748672 | ||||||
| chr13:31748674
|
C | T | 1 | a0001c0002t0002g0225 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+8968C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748674 | ||||||
| chr13:31748703
|
C | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.94+8997C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748703 | ||||||
| chr13:31748728
|
T | C | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245 | 3 | HG02572.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.94+9022T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748728 | ||||||
| chr13:31748758
|
G | A | 1 | a0006c0010t0001g0047 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.94+9052G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748758 | ||||||
| chr13:31748858
|
G | A | 1 | a0001c0001t0005g0152 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.94+9152G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31748858 | ||||||
| chr13:31749142
|
G | A | 116 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.95-9116G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749142 | ||||||
| chr13:31749143
|
T | A | 1 | a0001c0004t0001g0084 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.95-9115T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749143 | ||||||
| chr13:31749417
|
G | A | 3 | a0001c0001t0001g0271a0001c0002t0002g0272a0001c0002t0002g0274 | 3 | HG03490.hp2 NA19080.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.95-8841G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749417 | ||||||
| chr13:31749515
|
T | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 27 | HG00621.hp1 HG01243.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.95-8743T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749515 | ||||||
| chr13:31749547
|
T | C | 96 | a0001c0001t0001g0137a0001c0001t0001g0289a0001c0001t0001g0290others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.95-8711T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749547 | ||||||
| chr13:31749567
|
T | G | 215 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(212): Show | 216 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.95-8691T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749567 | ||||||
| chr13:31749632
|
C | T | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(368): Show | 374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.95-8626C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749632 | ||||||
| chr13:31749689
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(211): Show | 215 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.95-8569T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749689 | ||||||
| chr13:31749859
|
C | T | 118 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(115): Show | 118 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.95-8399C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749859 | ||||||
| chr13:31749922
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02040.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.95-8336G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749922 | ||||||
| chr13:31749925
|
A | T | 118 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(115): Show | 118 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.95-8333A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749925 | ||||||
| chr13:31749976
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.95-8282G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31749976 | ||||||
| chr13:31750156
|
C | T | 1 | a0001c0002t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.95-8102C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31750156 | ||||||
| chr13:31750187
|
C | T | 2 | a0001c0002t0002g0381a0001c0002t0002g0382 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.95-8071C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31750187 | ||||||
| chr13:31750251
|
G | A | 1 | a0002c0003t0003g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.95-8007G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31750251 | ||||||
| chr13:31750656
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(211): Show | 215 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.95-7602T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31750656 | ||||||
| chr13:31750690
|
A | T | 17 | a0001c0001t0001g0271a0001c0001t0001g0367a0001c0001t0001g0372others(14): Show | 17 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-7568A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31750690 | ||||||
| chr13:31750707
|
A | C | 4 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0239others(1): Show | 4 | HG02922.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-7551A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31750707 | ||||||
| chr13:31750787
|
C | A | 17 | a0001c0001t0001g0271a0001c0001t0001g0367a0001c0001t0001g0372others(14): Show | 17 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-7471C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31750787 | ||||||
| chr13:31750796
|
C | G | 1 | a0001c0001t0003g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.95-7462C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31750796 | ||||||
| chr13:31751014
|
G | A | 96 | a0001c0001t0001g0137a0001c0001t0001g0289a0001c0001t0001g0290others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.95-7244G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751014 | ||||||
| chr13:31751070
|
A | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(113): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.95-7188A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751070 | ||||||
| chr13:31751160
|
C | T | 96 | a0001c0001t0001g0137a0001c0001t0001g0289a0001c0001t0001g0290others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.95-7098C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751160 | ||||||
| chr13:31751161
|
G | A | 1 | a0001c0002t0002g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.95-7097G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751161 | ||||||
| chr13:31751309
|
T | TTA | 17 | a0001c0001t0001g0271a0001c0001t0001g0367a0001c0001t0001g0372others(14): Show | 17 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-6938_95-6937dup others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31751309 | |||||
| chr13:31751322
|
C | T | 1 | a0009c0006t0001g0258 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.95-6936C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751322 | ||||||
| chr13:31751504
|
C | G | 1 | a0001c0001t0004g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.95-6754C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751504 | ||||||
| chr13:31751561
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.95-6697A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751561 | ||||||
| chr13:31751623
|
C | A | 3 | a0001c0001t0001g0367a0001c0002t0002g0252a0001c0002t0002g0253 | 3 | HG02451.hp1 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.95-6635C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751623 | ||||||
| chr13:31751845
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.95-6413G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31751845 | ||||||
| chr13:31752000
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.95-6258G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752000 | ||||||
| chr13:31752160
|
T | A | 1 | a0001c0001t0002g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.95-6098T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752160 | ||||||
| chr13:31752214
|
T | C | 1 | a0002c0003t0003g0374 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.95-6044T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752214 | ||||||
| chr13:31752246
|
C | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0032others(41): Show | 45 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.95-6012C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752246 | ||||||
| chr13:31752277
|
G | C | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(94): Show | 97 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.95-5981G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752277 | ||||||
| chr13:31752283
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.95-5975T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752283 | ||||||
| chr13:31752465
|
A | G | 16 | a0001c0001t0001g0367a0001c0001t0001g0372a0001c0002t0002g0013others(13): Show | 16 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.95-5793A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752465 | ||||||
| chr13:31752551
|
AAAC | A | 96 | a0001c0001t0001g0137a0001c0001t0001g0358a0001c0001t0004g0243others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.95-5691_95-5689del others(3): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31752551 | |||||
| chr13:31752714
|
C | T | 78 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(75): Show | 78 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.95-5544C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752714 | ||||||
| chr13:31752737
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.95-5521G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752737 | ||||||
| chr13:31752776
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.95-5482G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752776 | ||||||
| chr13:31752780
|
G | C | 40 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 40 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.95-5478G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752780 | ||||||
| chr13:31752785
|
A | G | 125 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(122): Show | 125 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.95-5473A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752785 | ||||||
| chr13:31752854
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.95-5404T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752854 | ||||||
| chr13:31752954
|
A | G | 116 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.95-5304A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752954 | ||||||
| chr13:31752990
|
C | T | 1 | a0001c0002t0002g0380 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.95-5268C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31752990 | ||||||
| chr13:31753025
|
C | T | 1 | a0001c0011t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.95-5233C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31753025 | ||||||
| chr13:31753080
|
C | T | 93 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(90): Show | 94 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-5178C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31753080 | ||||||
| chr13:31753082
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.95-5176C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31753082 | ||||||
| chr13:31753165
|
C | A | 2 | a0001c0002t0002g0295a0001c0002t0002g0362 | 2 | NA18977.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.95-5093C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31753165 | ||||||
| chr13:31753258
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.95-5000T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31753258 | ||||||
| chr13:31753321
|
G | A | 2 | a0001c0002t0002g0092a0001c0002t0002g0093 | 2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.95-4937G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31753321 | ||||||
| chr13:31753328
|
A | G | 1 | a0001c0002t0002g0357 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.95-4930A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31753328 | ||||||
| chr13:31753427
|
C | T | 1 | a0002c0003t0003g0371 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.95-4831C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31753427 | ||||||
| chr13:31753828
|
TG | T | 3 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0013t0002g0012 | 3 | HG02451.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.95-4428delG | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31753828 | |||||
| chr13:31754077
|
T | G | 6 | a0002c0003t0003g0049a0002c0003t0003g0050a0002c0003t0003g0051others(3): Show | 6 | HG00609.hp1 HG02027.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4181T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754077 | ||||||
| chr13:31754084
|
T | C | 81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.95-4174T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754084 | ||||||
| chr13:31754191
|
G | A | 79 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(76): Show | 79 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.95-4067G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754191 | ||||||
| chr13:31754245
|
A | T | 6 | a0001c0002t0002g0351a0001c0002t0002g0352a0001c0002t0002g0353others(3): Show | 6 | NA18939.hp1 NA18947.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4013A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754245 | ||||||
| chr13:31754348
|
T | C | 1 | a0001c0002t0002g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.95-3910T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754348 | ||||||
| chr13:31754391
|
C | T | 1 | a0001c0001t0004g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.95-3867C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754391 | ||||||
| chr13:31754402
|
G | A | 4 | a0001c0002t0002g0373a0001c0011t0001g0254a0001c0015t0003g0376others(1): Show | 4 | HG01175.hp1 HG01243.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3856G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754402 | ||||||
| chr13:31754460
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.95-3798G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754460 | ||||||
| chr13:31754547
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.95-3711G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754547 | ||||||
| chr13:31754551
|
C | T | 82 | a0001c0002t0001g0350a0001c0002t0002g0003a0001c0002t0002g0005others(79): Show | 83 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.95-3707C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754551 | ||||||
| chr13:31754831
|
G | A | 11 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0100others(8): Show | 11 | HG01175.hp1 HG01243.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-3427G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754831 | ||||||
| chr13:31754902
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(107): Show | 112 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.95-3356C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754902 | ||||||
| chr13:31754981
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0147others(61): Show | 65 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.95-3277C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754981 | ||||||
| chr13:31755018
|
C | T | 81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.95-3240C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755018 | ||||||
| chr13:31755106
|
A | T | 93 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(90): Show | 94 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-3152A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755106 | ||||||
| chr13:31755186
|
A | C | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG02486.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.95-3072A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755186 | ||||||
| chr13:31755408
|
C | T | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.95-2850C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755408 | ||||||
| chr13:31755538
|
C | T | 4 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0240others(1): Show | 4 | HG01496.hp1 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2720C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755538 | ||||||
| chr13:31755717
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.95-2541A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755717 | ||||||
| chr13:31755897
|
G | A | 93 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(90): Show | 94 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-2361G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755897 | ||||||
| chr13:31755934
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.95-2324G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755934 | ||||||
| chr13:31755976
|
C | T | 1 | a0001c0004t0001g0082 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.95-2282C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31755976 | ||||||
| chr13:31756042
|
G | A | 81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.95-2216G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756042 | ||||||
| chr13:31756076
|
C | CCTCCCTA others(9): Show |
81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.95-2180_95-2179ins others(16): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31756076 | |||||
| chr13:31756089
|
T | C | 1 | a0001c0002t0002g0231 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.95-2169T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756089 | ||||||
| chr13:31756134
|
C | T | 174 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(171): Show | 175 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.95-2124C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756134 | ||||||
| chr13:31756195
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.95-2063G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756195 | ||||||
| chr13:31756217
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.95-2041C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756217 | ||||||
| chr13:31756241
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.95-2017G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756241 | ||||||
| chr13:31756257
|
G | A | 4 | a0001c0002t0002g0136a0001c0002t0002g0380a0001c0002t0002g0381others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-2001G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756257 | ||||||
| chr13:31756274
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.95-1984C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756274 | ||||||
| chr13:31756284
|
C | T | 81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.95-1974C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756284 | ||||||
| chr13:31756409
|
C | T | 81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.95-1849C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756409 | ||||||
| chr13:31756459
|
C | T | 81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.95-1799C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756459 | ||||||
| chr13:31756479
|
C | G | 1 | a0001c0002t0002g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.95-1779C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756479 | ||||||
| chr13:31756547
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.95-1711C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756547 | ||||||
| chr13:31756589
|
A | G | 1 | a0002c0003t0003g0287 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95-1669A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756589 | ||||||
| chr13:31756619
|
C | T | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.95-1639C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756619 | ||||||
| chr13:31756621
|
A | AT | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0031others(166): Show | 171 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.95-1619dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31756621 | |||||
| chr13:31756621
|
A | ATT | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(3): Show | 6 | HG01192.hp1 HG02074.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-1620_95-1619dup others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31756621 | |||||
| chr13:31756621
|
AT | A | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.95-1619delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 31756621 | |||||
| chr13:31756662
|
T | C | 247 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 248 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.95-1596T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756662 | ||||||
| chr13:31756857
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1401G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756857 | ||||||
| chr13:31756899
|
G | T | 3 | a0001c0002t0002g0343a0001c0002t0002g0344a0001c0002t0002g0345 | 3 | NA18984.hp1 NA18999.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.95-1359G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756899 | ||||||
| chr13:31756931
|
A | T | 93 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(90): Show | 94 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-1327A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756931 | ||||||
| chr13:31756969
|
A | G | 3 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0238 | 3 | HG02717.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.95-1289A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31756969 | ||||||
| chr13:31757016
|
G | T | 2 | a0001c0004t0001g0134a0001c0004t0001g0135 | 2 | HG00280.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.95-1242G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757016 | ||||||
| chr13:31757024
|
C | G | 1 | a0001c0002t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.95-1234C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757024 | ||||||
| chr13:31757156
|
C | T | 1 | a0002c0003t0003g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-1102C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757156 | ||||||
| chr13:31757457
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-801G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757457 | ||||||
| chr13:31757644
|
C | T | 93 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(90): Show | 94 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-614C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757644 | ||||||
| chr13:31757876
|
A | G | 81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.95-382A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757876 | ||||||
| chr13:31757889
|
T | G | 16 | a0001c0001t0001g0372a0001c0002t0002g0013a0001c0002t0002g0014others(13): Show | 16 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.95-369T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757889 | ||||||
| chr13:31757907
|
C | G | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 35 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.95-351C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757907 | ||||||
| chr13:31757975
|
T | C | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(376): Show | 382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.95-283T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31757975 | ||||||
| chr13:31758046
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.95-212C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31758046 | ||||||
| chr13:31758057
|
G | C | 1 | a0002c0003t0003g0083 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.95-201G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31758057 | ||||||
| chr13:31758080
|
G | A | 93 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(90): Show | 94 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-178G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31758080 | ||||||
| chr13:31758155
|
C | G | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 39 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.95-103C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31758155 | ||||||
| chr13:31758173
|
T | C | 1 | a0001c0001t0004g0016 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.95-85T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31758173 | ||||||
| chr13:31758419
|
C | T | 77 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(74): Show | 77 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.241+15C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758419 | ||||||
| chr13:31758524
|
T | C | 242 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(239): Show | 243 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.241+120T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758524 | ||||||
| chr13:31758543
|
T | C | 93 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(90): Show | 94 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.241+139T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758543 | ||||||
| chr13:31758661
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.241+257C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758661 | ||||||
| chr13:31758707
|
C | T | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.241+303C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758707 | ||||||
| chr13:31758763
|
A | C | 1 | a0001c0002t0002g0373 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.241+359A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758763 | ||||||
| chr13:31758773
|
C | T | 1 | a0002c0003t0003g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.241+369C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758773 | ||||||
| chr13:31758862
|
A | T | 1 | a0001c0002t0002g0055 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.241+458A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758862 | ||||||
| chr13:31758925
|
G | A | 4 | a0001c0002t0002g0015a0001c0002t0002g0270a0001c0002t0002g0273others(1): Show | 4 | HG01891.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+521G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31758925 | ||||||
| chr13:31759025
|
T | C | 77 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(74): Show | 77 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.241+621T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759025 | ||||||
| chr13:31759047
|
C | CA | 81 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.241+656dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759047 | |||||
| chr13:31759047
|
CA | C | 9 | a0001c0001t0001g0019a0001c0002t0002g0341a0001c0002t0002g0342others(6): Show | 9 | HG02280.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+656delA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759047 | |||||
| chr13:31759061
|
T | A | 77 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(74): Show | 77 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.241+657T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759061 | ||||||
| chr13:31759077
|
G | A | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.241+673G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759077 | ||||||
| chr13:31759125
|
T | C | 77 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(74): Show | 77 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.241+721T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759125 | ||||||
| chr13:31759264
|
GT | G | 4 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0239others(1): Show | 4 | HG02922.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+861delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759264 | ||||||
| chr13:31759285
|
C | T | 77 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(74): Show | 77 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.241+881C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759285 | ||||||
| chr13:31759294
|
G | A | 77 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(74): Show | 77 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.241+890G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759294 | ||||||
| chr13:31759375
|
G | GAGAA | 22 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0030others(19): Show | 23 | HG01069.hp2 HG01071.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.241+1039_241+1042d others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(1): Show |
35 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0118others(32): Show | 36 | HG00099.hp2 HG00621.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.241+1035_241+1042d others(10): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(5): Show |
28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0107others(25): Show | 28 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.241+1031_241+1042d others(14): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(9): Show |
21 | a0001c0001t0001g0031a0001c0001t0001g0117a0001c0001t0001g0148others(18): Show | 21 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.241+1027_241+1042d others(18): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(13): Show |
21 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(18): Show | 21 | HG00544.hp1 HG01106.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.241+1023_241+1042d others(22): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(17): Show |
7 | a0001c0001t0001g0006a0001c0001t0001g0108a0001c0001t0001g0109others(4): Show | 7 | HG02132.hp2 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+1019_241+1042d others(26): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(21): Show |
3 | a0001c0001t0001g0147a0001c0001t0001g0178a0001c0004t0001g0280 | 3 | HG02027.hp1 HG02155.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.241+1015_241+1042d others(30): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(40): Show |
1 | a0001c0002t0002g0339 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.241+973_241+1019du others(48): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(44): Show |
1 | a0001c0001t0002g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.241+973_241+1023du others(52): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(52): Show |
4 | a0001c0002t0002g0013a0001c0002t0002g0336a0002c0003t0003g0028others(1): Show | 4 | HG02129.hp1 HG02300.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+973_241+1031du others(60): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(56): Show |
4 | a0001c0002t0002g0379a0001c0015t0003g0376a0002c0003t0003g0133others(1): Show | 4 | HG01243.hp1 HG02015.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+973_241+1035du others(64): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(57): Show |
2 | a0001c0001t0001g0358a0001c0001t0002g0120 | 2 | HG02970.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.241+979_241+1042du others(65): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(60): Show |
4 | a0001c0002t0002g0005a0001c0002t0002g0325a0001c0002t0002g0346others(1): Show | 4 | NA18967.hp1 NA19001.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+973_241+1039du others(68): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(61): Show |
2 | a0001c0001t0001g0137a0001c0002t0002g0363 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.241+975_241+1042du others(69): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(64): Show |
4 | a0001c0001t0002g0121a0001c0002t0002g0296a0001c0002t0002g0375others(1): Show | 4 | HG02109.hp2 NA18946.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+972_241+1042du others(72): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(65): Show |
6 | a0001c0001t0001g0019a0001c0002t0002g0249a0001c0002t0002g0311others(3): Show | 6 | HG02027.hp2 HG02148.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(74): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(68): Show |
4 | a0001c0001t0001g0036a0001c0002t0002g0272a0002c0003t0003g0073others(1): Show | 4 | HG02818.hp1 HG03209.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(77): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(69): Show |
5 | a0001c0001t0004g0243a0001c0002t0002g0310a0002c0003t0003g0022others(2): Show | 5 | HG01256.hp1 HG02572.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(78): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(72): Show |
3 | a0002c0003t0003g0072a0002c0003t0003g0083a0002c0003t0003g0102 | 3 | NA18949.hp1 NA18994.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(81): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(73): Show |
13 | a0001c0001t0002g0017a0001c0001t0004g0016a0001c0002t0001g0350others(10): Show | 13 | HG00438.hp2 HG00673.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(82): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(76): Show |
2 | a0001c0002t0002g0312a0002c0003t0003g0059 | 2 | NA18948.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(85): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(77): Show |
5 | a0001c0001t0001g0141a0001c0002t0002g0303a0001c0002t0002g0304others(2): Show | 5 | HG00609.hp2 HG00741.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(86): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(81): Show |
3 | a0001c0002t0002g0297a0001c0002t0002g0351a0001c0002t0002g0373 | 3 | HG00099.hp1 HG01175.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(90): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(85): Show |
5 | a0001c0001t0001g0140a0001c0002t0002g0015a0001c0002t0002g0302others(2): Show | 5 | HG00438.hp1 HG01891.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(94): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(89): Show |
1 | a0002c0003t0003g0089 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.241+1042_241+1043i others(98): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(88): Show |
1 | a0001c0002t0002g0343 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.241+1042_241+1043i others(97): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(84): Show |
1 | a0001c0002t0002g0344 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.241+1042_241+1043i others(93): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(86): Show |
1 | a0001c0002t0002g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.241+1042_241+1043i others(95): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(76): Show |
3 | a0001c0002t0002g0315a0001c0002t0006g0314a0002c0003t0003g0060 | 3 | HG01433.hp1 HG03704.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(85): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(84): Show |
1 | a0001c0002t0002g0313 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.241+1042_241+1043i others(93): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(87): Show |
1 | a0001c0001t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.241+1042_241+1043i others(96): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(72): Show |
2 | a0001c0002t0002g0003a0002c0003t0003g0371 | 3 | HG01069.hp1 HG03017.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(81): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(76): Show |
2 | a0001c0001t0001g0103a0001c0002t0002g0092 | 2 | HG02132.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(85): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(84): Show |
2 | a0001c0001t0001g0039a0001c0002t0002g0353 | 2 | NA18941.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(93): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(88): Show |
2 | a0001c0001t0001g0101a0001c0002t0002g0273 | 2 | HG02723.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(97): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(87): Show |
1 | a0003c0005t0002g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.241+1042_241+1043i others(96): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(67): Show |
2 | a0002c0003t0003g0023a0002c0003t0003g0037 | 2 | HG01515.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(76): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(68): Show |
8 | a0001c0001t0001g0372a0001c0001t0004g0244a0001c0002t0002g0295others(5): Show | 8 | HG00609.hp1 HG03486.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(77): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(72): Show |
9 | a0001c0002t0002g0251a0001c0002t0002g0298a0001c0002t0002g0318others(6): Show | 9 | HG01358.hp1 HG01943.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(81): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(76): Show |
4 | a0001c0001t0002g0018a0001c0002t0002g0316a0001c0002t0002g0317others(1): Show | 4 | HG01496.hp1 HG02109.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+1042_241+1043i others(85): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(80): Show |
1 | a0002c0003t0003g0050 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.241+1042_241+1043i others(89): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(63): Show |
1 | a0001c0002t0002g0327 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.241+1039_241+1040i others(72): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(64): Show |
6 | a0001c0002t0002g0119a0001c0002t0002g0300a0001c0002t0002g0324others(3): Show | 6 | HG01074.hp1 HG01515.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+1039_241+1040i others(73): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(68): Show |
10 | a0001c0001t0001g0142a0001c0002t0002g0231a0001c0002t0002g0322others(7): Show | 10 | HG01257.hp2 HG01975.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.241+1039_241+1040i others(77): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(72): Show |
5 | a0001c0001t0002g0122a0001c0002t0002g0093a0001c0002t0002g0288others(2): Show | 5 | HG01255.hp2 HG02040.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+1039_241+1040i others(81): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(76): Show |
3 | a0001c0002t0002g0354a0001c0002t0002g0368a0002c0003t0003g0071 | 3 | HG02074.hp1 HG03041.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.241+1039_241+1040i others(85): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(80): Show |
1 | a0001c0002t0002g0383 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.241+1039_241+1040i others(89): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(88): Show |
1 | a0002c0003t0003g0377 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.241+1039_241+1040i others(97): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(67): Show |
1 | a0001c0002t0002g0326 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.241+1039_241+1040i others(76): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(71): Show |
1 | a0001c0002t0002g0357 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.241+1039_241+1040i others(80): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(75): Show |
1 | a0001c0002t0002g0361 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.241+1039_241+1040i others(84): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(60): Show |
4 | a0001c0001t0004g0245a0001c0002t0002g0270a0001c0002t0002g0331others(1): Show | 4 | HG02080.hp2 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+1035_241+1036i others(69): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(64): Show |
6 | a0001c0001t0001g0033a0001c0002t0002g0034a0001c0013t0002g0012others(3): Show | 6 | HG02451.hp2 HG02970.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.241+1035_241+1036i others(73): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(68): Show |
8 | a0001c0001t0001g0032a0001c0001t0001g0246a0001c0002t0002g0286others(5): Show | 8 | HG02083.hp1 HG03209.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.241+1035_241+1036i others(77): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(72): Show |
4 | a0001c0001t0002g0240a0001c0002t0002g0328a0001c0002t0002g0342others(1): Show | 4 | NA18906.hp2 NA18964.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+1035_241+1036i others(81): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(71): Show |
1 | a0002c0003t0003g0234 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.241+1035_241+1036i others(80): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(55): Show |
1 | a0001c0002t0002g0337 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.241+1031_241+1032i others(64): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(56): Show |
2 | a0001c0001t0001g0139a0001c0002t0002g0232 | 2 | HG01169.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.241+1031_241+1032i others(65): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(59): Show |
1 | a0001c0002t0002g0014 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.241+1031_241+1032i others(68): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(60): Show |
2 | a0001c0002t0002g0335a0002c0003t0003g0068 | 2 | HG00673.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.241+1031_241+1032i others(69): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(64): Show |
3 | a0001c0001t0001g0035a0001c0002t0002g0334a0002c0003t0003g0067 | 3 | HG00558.hp1 NA18954.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.241+1031_241+1032i others(73): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(52): Show |
2 | a0001c0002t0002g0229a0001c0002t0006g0338 | 2 | HG03453.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.241+1027_241+1028i others(61): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(56): Show |
2 | a0001c0002t0002g0366a0002c0003t0003g0104 | 2 | HG01074.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.241+1027_241+1028i others(65): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(60): Show |
2 | a0001c0002t0002g0247a0002c0003t0003g0069 | 2 | HG02258.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.241+1027_241+1028i others(69): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(62): Show |
1 | a0002c0003t0003g0378 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.241+1026_241+1027i others(71): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAAGA others(60): Show |
1 | a0001c0001t0004g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.241+1014_241+1015i others(69): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAGAA others(8): Show |
1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.241+975_241+976ins others(15): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAGAA others(71): Show |
1 | a0001c0002t0002g0340 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.241+975_241+976ins others(78): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAAGGA others(9): Show |
1 | a0001c0001t0003g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.241+975_241+976ins others(16): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GAGAGAAA others(3): Show |
1 | a0001c0001t0008g0217 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.241+974_241+975ins others(10): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
G | GGAAAGAA others(8): Show |
1 | a0001c0001t0001g0218 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.241+971_241+972ins others(15): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759375 | ||||||
| chr13:31759375
|
GAGAA | G | 14 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(11): Show | 14 | HG00741.hp1 HG01099.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.241+1039_241+1042d others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
GAGAAAGA others(1): Show |
G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0220others(2): Show | 5 | HG03130.hp1 NA18979.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.241+1035_241+1042d others(10): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
GAGAAAGA others(5): Show |
G | 2 | a0001c0001t0001g0213a0001c0001t0001g0221 | 2 | NA18983.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.241+1031_241+1042d others(14): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
GAGAAAGA others(9): Show |
G | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0235 | 3 | NA18939.hp2 NA19074.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.241+1027_241+1042d others(18): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759375
|
GAGAAAGA others(13): Show |
G | 1 | a0001c0001t0001g0216 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.241+1023_241+1042d others(22): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759375 | |||||
| chr13:31759378
|
A | AAAGAAAG others(48): Show |
2 | a0001c0001t0001g0143a0001c0002t0002g0365 | 2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.241+977_241+1031du others(56): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759378 | |||||
| chr13:31759378
|
A | AAAGAAAG others(52): Show |
5 | a0001c0001t0002g0004a0001c0002t0002g0146a0001c0002t0002g0284others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+977_241+1035du others(60): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759378 | |||||
| chr13:31759378
|
A | AAAGAAAG others(56): Show |
1 | a0001c0002t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.241+977_241+1039du others(64): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759378 | |||||
| chr13:31759378
|
A | AAAGAAAG others(64): Show |
3 | a0001c0002t0002g0274a0002c0003t0003g0090a0003c0005t0002g0242 | 3 | HG02572.hp2 HG02886.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.241+1042_241+1043i others(73): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759378 | |||||
| chr13:31759378
|
A | AAAGAAAG others(55): Show |
1 | a0001c0002t0002g0333 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.241+1035_241+1036i others(64): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759378 | |||||
| chr13:31759382
|
A | AAAGAAAG others(52): Show |
1 | a0001c0002t0002g0255 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.241+981_241+1039du others(60): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759382 | |||||
| chr13:31759386
|
A | AAAGAAAG others(52): Show |
1 | a0002c0003t0003g0075 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.241+984_241+1042du others(60): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759386 | |||||
| chr13:31759386
|
A | AAAGAAAG others(60): Show |
1 | a0002c0003t0003g0074 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.241+1042_241+1043i others(69): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759386 | |||||
| chr13:31759401
|
G | GAAAGAAA others(3): Show |
1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.241+999_241+1008du others(11): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759401 | |||||
| chr13:31759438
|
A | AAAGAAAG others(81): Show |
1 | a0001c0001t0001g0038 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.241+1042_241+1043i others(90): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31759438 | |||||
| chr13:31759443
|
A | T | 1 | a0001c0002t0002g0364 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.241+1039A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759443 | ||||||
| chr13:31759444
|
A | G | 1 | a0001c0002t0002g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.241+1040A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759444 | ||||||
| chr13:31759446
|
A | AAAGAAAG others(24): Show |
1 | a0001c0001t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.241+1042_241+1043i others(33): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759446 | ||||||
| chr13:31759447
|
T | A | 22 | a0001c0001t0001g0103a0001c0001t0002g0017a0001c0001t0002g0018others(19): Show | 22 | HG01106.hp2 HG01175.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.241+1043T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759447 | ||||||
| chr13:31759451
|
G | A | 1 | a0001c0002t0002g0005 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.241+1047G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759451 | ||||||
| chr13:31759956
|
G | T | 95 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(92): Show | 96 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.241+1552G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759956 | ||||||
| chr13:31759978
|
C | T | 1 | a0001c0002t0002g0339 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.241+1574C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31759978 | ||||||
| chr13:31760065
|
GTGT | G | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.242-1648_242-1646d others(5): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31760065 | |||||
| chr13:31760068
|
T | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 35 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.242-1656T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760068 | ||||||
| chr13:31760073
|
G | GT | 4 | a0001c0001t0002g0004a0001c0001t0002g0120a0001c0001t0002g0121others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-1649dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31760073 | |||||
| chr13:31760073
|
G | GTTGT | 75 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(72): Show | 75 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-1624_242-1621d others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31760073 | |||||
| chr13:31760073
|
GTTGTTTG others(5): Show |
G | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.242-1632_242-1621d others(14): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr13 | 31760073 | |||||
| chr13:31760137
|
G | A | 2 | a0002c0003t0003g0074a0002c0003t0003g0075 | 2 | HG00735.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.242-1587G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760137 | ||||||
| chr13:31760300
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.242-1424G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760300 | ||||||
| chr13:31760338
|
G | A | 8 | a0002c0003t0003g0054a0002c0003t0003g0056a0002c0003t0003g0060others(5): Show | 8 | HG02015.hp1 NA18946.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-1386G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760338 | ||||||
| chr13:31760385
|
T | C | 170 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(167): Show | 171 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.242-1339T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760385 | ||||||
| chr13:31760450
|
C | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 35 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.242-1274C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760450 | ||||||
| chr13:31760470
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.242-1254G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760470 | ||||||
| chr13:31760540
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.242-1184C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760540 | ||||||
| chr13:31760618
|
C | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0120a0001c0001t0002g0121others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-1106C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760618 | ||||||
| chr13:31760628
|
A | C | 3 | a0001c0002t0002g0284a0001c0002t0002g0285a0001c0002t0002g0286 | 3 | HG02683.hp2 HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.242-1096A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760628 | ||||||
| chr13:31760664
|
G | A | 95 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(92): Show | 96 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.242-1060G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760664 | ||||||
| chr13:31760732
|
G | T | 181 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(178): Show | 182 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.242-992G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760732 | ||||||
| chr13:31760734
|
T | C | 170 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(167): Show | 171 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.242-990T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760734 | ||||||
| chr13:31760839
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.242-885A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31760839 | ||||||
| chr13:31761009
|
T | C | 242 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(239): Show | 243 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.242-715T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761009 | ||||||
| chr13:31761038
|
G | A | 1 | a0001c0002t0002g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.242-686G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761038 | ||||||
| chr13:31761203
|
C | T | 1 | a0001c0002t0002g0359 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.242-521C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761203 | ||||||
| chr13:31761364
|
T | C | 1 | a0001c0002t0002g0005 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.242-360T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761364 | ||||||
| chr13:31761388
|
G | T | 3 | a0002c0003t0003g0050a0002c0003t0003g0051a0002c0003t0003g0052 | 3 | HG00609.hp1 HG02155.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.242-336G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761388 | ||||||
| chr13:31761389
|
A | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(112): Show | 117 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.242-335A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761389 | ||||||
| chr13:31761496
|
A | T | 1 | a0001c0001t0001g0038 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.242-228A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761496 | ||||||
| chr13:31761616
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.242-108C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761616 | ||||||
| chr13:31761703
|
A | T | 75 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(72): Show | 75 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-21A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 2/17 | chr13 | 31761703 | ||||||
| chr13:31761850
|
T | C | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.319+49T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31761850 | ||||||
| chr13:31761903
|
C | T | 95 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(92): Show | 96 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.319+102C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31761903 | ||||||
| chr13:31762218
|
G | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(8): Show | 11 | HG01496.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.319+417G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31762218 | ||||||
| chr13:31762249
|
G | A | 70 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(67): Show | 70 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.319+448G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31762249 | ||||||
| chr13:31762349
|
G | A | 1 | a0001c0001t0001g0372 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.319+548G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31762349 | ||||||
| chr13:31762397
|
G | A | 96 | a0001c0001t0001g0137a0001c0001t0004g0243a0001c0001t0004g0244others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.319+596G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31762397 | ||||||
| chr13:31762404
|
GA | G | 6 | a0001c0002t0002g0136a0001c0002t0002g0373a0001c0002t0002g0380others(3): Show | 6 | HG01175.hp1 HG02109.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+605delA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31762404 | |||||
| chr13:31762509
|
T | C | 2 | a0001c0002t0002g0322a0001c0002t0002g0340 | 2 | HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.319+708T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31762509 | ||||||
| chr13:31762600
|
G | A | 71 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(68): Show | 71 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.319+799G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31762600 | ||||||
| chr13:31762894
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.319+1093T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31762894 | ||||||
| chr13:31763075
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.319+1274T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31763075 | ||||||
| chr13:31763081
|
CT | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.319+1300delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31763081 | |||||
| chr13:31763081
|
CTT | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 36 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.319+1299_319+1300d others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31763081 | |||||
| chr13:31763081
|
CTTTT | C | 58 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0002t0002g0379others(55): Show | 58 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.319+1297_319+1300d others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31763081 | |||||
| chr13:31763233
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.319+1432C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31763233 | ||||||
| chr13:31763324
|
G | A | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(349): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.319+1523G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31763324 | ||||||
| chr13:31763360
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.319+1559C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31763360 | ||||||
| chr13:31763610
|
AGAAG | A | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 36 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.320-1426_320-1423d others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31763610 | ||||||
| chr13:31763909
|
C | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.320-1128C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31763909 | ||||||
| chr13:31763953
|
T | A | 18 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(15): Show | 18 | HG01175.hp1 HG01243.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.320-1084T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31763953 | ||||||
| chr13:31764197
|
C | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.320-840C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764197 | ||||||
| chr13:31764242
|
T | TTC | 3 | a0001c0001t0001g0137a0001c0001t0002g0018a0001c0015t0003g0376 | 3 | HG01243.hp1 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.320-794_320-793dup others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764242 | |||||
| chr13:31764243
|
T | TCA | 75 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0045others(72): Show | 75 | HG00558.hp2 HG01071.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.320-749_320-748dup others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
T | TCACA | 31 | a0001c0001t0001g0006a0001c0001t0001g0163a0001c0001t0001g0165others(28): Show | 31 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.320-751_320-748dup others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
T | TCACACA | 15 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0041others(12): Show | 16 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.320-753_320-748dup others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
T | TCACACAC others(1): Show |
4 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0260others(1): Show | 4 | HG03130.hp1 NA18950.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-755_320-748dup others(8): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
T | TCACACAC others(3): Show |
7 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG00280.hp1 NA18977.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.320-757_320-748dup others(10): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
T | TCACACAC others(5): Show |
5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | NA18968.hp2 NA18982.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-759_320-748dup others(12): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
T | TCACACAC others(9): Show |
1 | a0001c0001t0001g0002 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.320-763_320-748dup others(16): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
T | TCTCACA | 3 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0002g0122 | 3 | HG02109.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.320-793_320-792ins others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
TCA | T | 24 | a0001c0001t0001g0142a0001c0001t0001g0182a0001c0001t0001g0256others(21): Show | 24 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.320-749_320-748del others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
TCACA | T | 14 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0086others(11): Show | 14 | HG02300.hp1 NA18906.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.320-751_320-748del others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
TCACACAC others(1): Show |
T | 6 | a0001c0001t0001g0010a0001c0001t0001g0237a0001c0004t0001g0127others(3): Show | 6 | HG02723.hp2 HG04228.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.320-755_320-748del others(8): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
TCACACAC others(3): Show |
T | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.320-757_320-748del others(10): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764243
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.320-759_320-748del others(12): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764243 | |||||
| chr13:31764245
|
A | T | 1 | a0001c0002t0002g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.320-792A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764245 | ||||||
| chr13:31764284
|
C | CACACACA others(3): Show |
1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.320-748_320-747ins others(10): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764284 | |||||
| chr13:31764284
|
C | CACACACA others(1): Show |
3 | a0001c0001t0001g0103a0002c0003t0003g0083a0008c0007t0003g0061 | 3 | HG02683.hp1 NA18949.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.320-748_320-747ins others(8): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764284 | |||||
| chr13:31764284
|
C | CACACAT | 15 | a0001c0002t0002g0379a0002c0003t0003g0048a0002c0003t0003g0066others(12): Show | 15 | HG00438.hp1 HG01074.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.320-748_320-747ins others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764284 | |||||
| chr13:31764284
|
C | CACAT | 9 | a0002c0003t0003g0022a0002c0003t0003g0028a0002c0003t0003g0029others(6): Show | 9 | HG01433.hp2 HG01515.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.320-750_320-749ins others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764284 | |||||
| chr13:31764284
|
C | CAT | 30 | a0002c0003t0003g0021a0002c0003t0003g0023a0002c0003t0003g0024others(27): Show | 30 | HG00609.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.320-752_320-751ins others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764284 | |||||
| chr13:31764284
|
C | T | 1 | a0002c0003t0003g0067 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.320-753C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764284 | ||||||
| chr13:31764411
|
TCTG | T | 59 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0002t0002g0379others(56): Show | 59 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.320-625_320-623del others(3): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764411 | ||||||
| chr13:31764707
|
TACTC | T | 88 | a0001c0002t0001g0350a0001c0002t0002g0003a0001c0002t0002g0005others(85): Show | 89 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.320-328_320-325del others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 31764707 | |||||
| chr13:31764748
|
C | T | 5 | a0001c0001t0001g0178a0001c0001t0001g0182a0001c0001t0001g0199others(2): Show | 5 | HG00544.hp1 HG00621.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-289C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764748 | ||||||
| chr13:31764836
|
G | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0039 | 3 | NA18941.hp2 NA18982.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.320-201G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764836 | ||||||
| chr13:31764863
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.320-174T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764863 | ||||||
| chr13:31764875
|
G | A | 59 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0002t0002g0379others(56): Show | 59 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.320-162G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764875 | ||||||
| chr13:31764888
|
A | G | 3 | a0001c0002t0002g0277a0001c0002t0002g0278a0001c0002t0002g0279 | 3 | NA18948.hp2 NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.320-149A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 3/17 | chr13 | 31764888 | ||||||
| chr13:31765159
|
T | A | 1 | a0001c0002t0002g0383 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.425+17T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765159 | ||||||
| chr13:31765245
|
C | T | 178 | a0001c0001t0001g0019a0001c0001t0001g0101a0001c0001t0001g0103others(175): Show | 179 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.425+103C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765245 | ||||||
| chr13:31765267
|
C | A | 1 | a0001c0001t0002g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.425+125C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765267 | ||||||
| chr13:31765301
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.425+159A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765301 | ||||||
| chr13:31765328
|
T | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0032others(48): Show | 52 | HG00099.hp2 HG00735.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.425+186T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765328 | ||||||
| chr13:31765364
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.425+222G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765364 | ||||||
| chr13:31765367
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.425+225T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765367 | ||||||
| chr13:31765424
|
T | C | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(349): Show | 355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.425+282T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765424 | ||||||
| chr13:31765432
|
C | CT | 69 | a0001c0001t0001g0006a0001c0001t0001g0101a0001c0001t0001g0103others(66): Show | 69 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.425+301dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr13 | 31765432 | |||||
| chr13:31765432
|
CT | C | 97 | a0001c0001t0001g0019a0001c0001t0001g0137a0001c0001t0001g0237others(94): Show | 98 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.425+301delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr13 | 31765432 | |||||
| chr13:31765440
|
T | TG | 4 | a0001c0002t0002g0136a0001c0002t0002g0380a0001c0002t0002g0381others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.425+298_425+299ins others(1): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765440 | ||||||
| chr13:31765466
|
C | T | 4 | a0001c0002t0002g0136a0001c0002t0002g0380a0001c0002t0002g0381others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.425+324C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765466 | ||||||
| chr13:31765488
|
G | A | 43 | a0002c0003t0003g0021a0002c0003t0003g0022a0002c0003t0003g0023others(40): Show | 43 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.425+346G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765488 | ||||||
| chr13:31765658
|
T | A | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.426-298T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765658 | ||||||
| chr13:31765775
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.426-181C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765775 | ||||||
| chr13:31765890
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.426-66G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 4/17 | chr13 | 31765890 | ||||||
| chr13:31766038
|
G | A | 3 | a0001c0002t0002g0295a0001c0002t0002g0318a0001c0002t0002g0362 | 3 | NA18977.hp2 NA18989.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.497+11G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766038 | ||||||
| chr13:31766056
|
T | TA | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.497+37dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 31766056 | |||||
| chr13:31766121
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.497+94T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766121 | ||||||
| chr13:31766173
|
T | G | 1 | a0001c0001t0001g0358 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.497+146T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766173 | ||||||
| chr13:31766338
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0002g0170a0001c0001t0002g0172 | 3 | HG02280.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497+311G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766338 | ||||||
| chr13:31766345
|
T | G | 59 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0002t0002g0379others(56): Show | 59 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.497+318T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766345 | ||||||
| chr13:31766608
|
C | T | 2 | a0002c0003t0003g0029a0002c0003t0003g0037 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.497+581C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766608 | ||||||
| chr13:31766879
|
T | C | 5 | a0001c0001t0002g0004a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+852T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766879 | ||||||
| chr13:31766988
|
T | A | 1 | a0001c0001t0001g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.497+961T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766988 | ||||||
| chr13:31766994
|
C | T | 1 | a0001c0002t0002g0225 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.497+967C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31766994 | ||||||
| chr13:31767083
|
A | G | 1 | a0003c0005t0002g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.497+1056A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31767083 | ||||||
| chr13:31767477
|
T | C | 2 | a0001c0002t0002g0319a0001c0002t0007g0329 | 2 | HG02129.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.497+1450T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31767477 | ||||||
| chr13:31767487
|
G | A | 1 | a0001c0002t0002g0324 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.497+1460G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31767487 | ||||||
| chr13:31767584
|
T | A | 4 | a0002c0003t0003g0028a0002c0003t0003g0089a0002c0003t0003g0090others(1): Show | 4 | HG02572.hp2 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+1557T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31767584 | ||||||
| chr13:31767962
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.497+1935C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31767962 | ||||||
| chr13:31767983
|
C | T | 2 | a0001c0002t0002g0373a0001c0011t0001g0254 | 2 | HG01175.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.497+1956C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31767983 | ||||||
| chr13:31767987
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.497+1960T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31767987 | ||||||
| chr13:31768121
|
T | C | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.497+2094T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31768121 | ||||||
| chr13:31768135
|
T | A | 1 | a0001c0002t0002g0331 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.497+2108T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31768135 | ||||||
| chr13:31768303
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0192a0001c0001t0001g0267 | 4 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+2276C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31768303 | ||||||
| chr13:31768474
|
G | A | 14 | a0001c0002t0002g0007a0001c0002t0002g0013a0001c0002t0002g0014others(11): Show | 14 | HG00544.hp2 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.497+2447G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31768474 | ||||||
| chr13:31768841
|
C | A | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0239 | 3 | HG02922.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.497+2814C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31768841 | ||||||
| chr13:31769201
|
G | A | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.497+3174G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31769201 | ||||||
| chr13:31769382
|
C | T | 5 | a0002c0003t0003g0050a0002c0003t0003g0051a0002c0003t0003g0052others(2): Show | 5 | HG00609.hp1 HG02155.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+3355C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31769382 | ||||||
| chr13:31769721
|
C | T | 4 | a0001c0002t0002g0136a0001c0002t0002g0380a0001c0002t0002g0381others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+3694C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31769721 | ||||||
| chr13:31769763
|
C | CA | 4 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | NA18960.hp2 NA18963.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+3737dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 31769763 | |||||
| chr13:31769796
|
C | T | 1 | a0001c0002t0002g0157 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.497+3769C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31769796 | ||||||
| chr13:31769815
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.497+3788C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31769815 | ||||||
| chr13:31769858
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.497+3831A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31769858 | ||||||
| chr13:31769860
|
G | T | 23 | a0001c0001t0001g0150a0001c0001t0001g0159a0001c0001t0001g0160others(20): Show | 23 | HG00544.hp1 HG00621.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.497+3833G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31769860 | ||||||
| chr13:31769908
|
C | G | 4 | a0001c0002t0002g0136a0001c0002t0002g0380a0001c0002t0002g0381others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+3881C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31769908 | ||||||
| chr13:31770164
|
G | A | 30 | a0001c0001t0001g0019a0001c0001t0001g0237a0001c0001t0002g0004others(27): Show | 30 | HG01175.hp1 HG01243.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.497+4137G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31770164 | ||||||
| chr13:31770486
|
C | T | 12 | a0002c0003t0003g0021a0002c0003t0003g0022a0002c0003t0003g0023others(9): Show | 12 | HG00735.hp1 HG01167.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.498-4134C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31770486 | ||||||
| chr13:31770685
|
C | G | 1 | a0006c0010t0001g0047 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.498-3935C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31770685 | ||||||
| chr13:31770852
|
G | A | 91 | a0001c0001t0001g0137a0001c0002t0001g0350a0001c0002t0002g0003others(88): Show | 92 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.498-3768G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31770852 | ||||||
| chr13:31770864
|
G | C | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.498-3756G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31770864 | ||||||
| chr13:31770974
|
A | T | 7 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(4): Show | 7 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-3646A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31770974 | ||||||
| chr13:31771018
|
TG | T | 16 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(13): Show | 16 | HG01175.hp1 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.498-3601delG | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31771018 | ||||||
| chr13:31771071
|
G | A | 56 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0013t0002g0012others(53): Show | 56 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.498-3549G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31771071 | ||||||
| chr13:31771377
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.498-3243G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31771377 | ||||||
| chr13:31771427
|
A | T | 2 | a0001c0002t0002g0381a0001c0002t0002g0382 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.498-3193A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31771427 | ||||||
| chr13:31771488
|
C | T | 2 | a0001c0001t0001g0177a0001c0015t0003g0376 | 2 | HG01243.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.498-3132C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31771488 | ||||||
| chr13:31771615
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(258): Show | 263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.498-3005T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31771615 | ||||||
| chr13:31771791
|
T | TA | 6 | a0001c0001t0001g0088a0001c0001t0001g0143a0001c0001t0001g0226others(3): Show | 6 | HG01167.hp2 HG01243.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-2817dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 31771791 | |||||
| chr13:31771791
|
T | TAA | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(223): Show | 228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.498-2818_498-2817d others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 31771791 | |||||
| chr13:31771923
|
A | G | 56 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0013t0002g0012others(53): Show | 56 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.498-2697A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31771923 | ||||||
| chr13:31771949
|
C | CA | 82 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0358others(79): Show | 82 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.498-2662dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 31771949 | |||||
| chr13:31772007
|
T | TAA | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(258): Show | 263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.498-2613_498-2612i others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772007 | ||||||
| chr13:31772069
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.498-2551T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772069 | ||||||
| chr13:31772104
|
G | A | 56 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0013t0002g0012others(53): Show | 56 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.498-2516G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772104 | ||||||
| chr13:31772143
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0237 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.498-2477T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772143 | ||||||
| chr13:31772481
|
C | T | 3 | a0001c0002t0002g0277a0001c0002t0002g0278a0001c0002t0002g0279 | 3 | NA18948.hp2 NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.498-2139C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772481 | ||||||
| chr13:31772534
|
C | T | 4 | a0002c0003t0003g0028a0002c0003t0003g0089a0002c0003t0003g0090others(1): Show | 4 | HG02572.hp2 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-2086C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772534 | ||||||
| chr13:31772655
|
A | G | 2 | a0001c0002t0002g0373a0001c0011t0001g0254 | 2 | HG01175.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.498-1965A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772655 | ||||||
| chr13:31772787
|
C | T | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.498-1833C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772787 | ||||||
| chr13:31772799
|
G | T | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.498-1821G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772799 | ||||||
| chr13:31772881
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0008g0217 | 3 | NA18945.hp1 NA18969.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.498-1739C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772881 | ||||||
| chr13:31772917
|
T | A | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.498-1703T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772917 | ||||||
| chr13:31772931
|
G | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.498-1689G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31772931 | ||||||
| chr13:31773177
|
A | G | 2 | a0002c0003t0003g0072a0002c0003t0003g0073 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.498-1443A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31773177 | ||||||
| chr13:31773349
|
G | C | 1 | a0001c0002t0002g0156 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.498-1271G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31773349 | ||||||
| chr13:31773361
|
G | T | 2 | a0002c0003t0003g0377a0002c0003t0003g0378 | 2 | HG01106.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.498-1259G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31773361 | ||||||
| chr13:31773417
|
C | A | 1 | a0001c0002t0002g0373 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.498-1203C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31773417 | ||||||
| chr13:31773422
|
C | CT | 12 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0259others(9): Show | 12 | HG01071.hp2 HG01106.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.498-1187dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 31773422 | |||||
| chr13:31773546
|
C | T | 1 | a0001c0002t0002g0373 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.498-1074C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31773546 | ||||||
| chr13:31773774
|
A | G | 1 | a0002c0003t0003g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.498-846A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31773774 | ||||||
| chr13:31773899
|
T | G | 30 | a0001c0001t0001g0019a0001c0001t0001g0237a0001c0001t0002g0004others(27): Show | 30 | HG01175.hp1 HG01243.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.498-721T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31773899 | ||||||
| chr13:31774064
|
A | G | 4 | a0001c0002t0002g0136a0001c0002t0002g0380a0001c0002t0002g0381others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-556A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31774064 | ||||||
| chr13:31774222
|
T | C | 2 | a0001c0002t0002g0373a0001c0011t0001g0254 | 2 | HG01175.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.498-398T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31774222 | ||||||
| chr13:31774387
|
G | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(8): Show | 11 | HG01496.hp1 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-233G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31774387 | ||||||
| chr13:31774436
|
T | C | 96 | a0001c0001t0001g0137a0001c0001t0003g0098a0001c0001t0003g0099others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.498-184T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31774436 | ||||||
| chr13:31774478
|
C | T | 1 | a0002c0003t0003g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.498-142C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31774478 | ||||||
| chr13:31774722
|
T | C | 95 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(92): Show | 95 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.569+31T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 6/17 | chr13 | 31774722 | ||||||
| chr13:31774779
|
T | C | 1 | a0001c0002t0002g0156 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.569+88T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 6/17 | chr13 | 31774779 | ||||||
| chr13:31774850
|
C | T | 56 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0013t0002g0012others(53): Show | 56 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.569+159C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 6/17 | chr13 | 31774850 | ||||||
| chr13:31774880
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.569+189A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 6/17 | chr13 | 31774880 | ||||||
| chr13:31775044
|
A | T | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.570-274A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 6/17 | chr13 | 31775044 | ||||||
| chr13:31775198
|
G | A | 1 | a0001c0004t0001g0076 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.570-120G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 6/17 | chr13 | 31775198 | ||||||
| chr13:31775597
|
TCTGTGGC others(5): Show |
T | 3 | a0001c0002t0002g0034a0001c0002t0002g0166a0001c0002t0002g0253 | 3 | HG02451.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.641+210_641+221del others(12): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31775597 | |||||
| chr13:31775601
|
T | C | 4 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(1): Show | 4 | HG02145.hp2 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+212T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31775601 | ||||||
| chr13:31775655
|
A | T | 1 | a0001c0002t0002g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.641+266A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31775655 | ||||||
| chr13:31775826
|
C | T | 4 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(1): Show | 4 | HG02145.hp2 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+437C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31775826 | ||||||
| chr13:31775859
|
G | A | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.641+470G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31775859 | ||||||
| chr13:31775944
|
G | A | 7 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(4): Show | 7 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.641+555G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31775944 | ||||||
| chr13:31776005
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18968.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.641+616C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776005 | ||||||
| chr13:31776061
|
C | CTTCT | 81 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0033others(78): Show | 82 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.641+688_641+691dup others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776061 | |||||
| chr13:31776061
|
C | CTTCTTTC others(1): Show |
100 | a0001c0001t0001g0237a0001c0001t0002g0100a0001c0001t0002g0121others(97): Show | 101 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.641+684_641+691dup others(8): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776061 | |||||
| chr13:31776061
|
C | CTTCTTTC others(5): Show |
5 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(2): Show | 5 | HG01496.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+680_641+691dup others(12): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776061 | |||||
| chr13:31776061
|
C | CTTCTTTC others(9): Show |
3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0239 | 3 | HG02922.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.641+676_641+691dup others(16): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776061 | |||||
| chr13:31776061
|
C | CTTCTTTC others(13): Show |
1 | a0002c0012t0002g0124 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641+691_641+692ins others(20): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776061 | |||||
| chr13:31776061
|
C | CTTTCT | 32 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0106others(29): Show | 33 | HG00099.hp2 HG00735.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.641+674_641+675ins others(5): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776061 | |||||
| chr13:31776077
|
T | TTTCC | 34 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(31): Show | 34 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.641+696_641+699dup others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776077 | |||||
| chr13:31776081
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0040others(32): Show | 35 | HG00438.hp1 HG01074.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.641+692C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776081 | ||||||
| chr13:31776085
|
C | T | 12 | a0001c0001t0002g0240a0001c0001t0004g0243a0001c0001t0004g0244others(9): Show | 12 | HG01175.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.641+696C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776085 | ||||||
| chr13:31776089
|
T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0030others(32): Show | 35 | HG00438.hp1 HG01074.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.641+700T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776089 | ||||||
| chr13:31776093
|
T | C | 9 | a0001c0001t0004g0245a0001c0002t0002g0136a0001c0002t0002g0373others(6): Show | 9 | HG01175.hp1 HG02622.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.641+704T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776093 | ||||||
| chr13:31776096
|
C | CCTTCCTT others(4): Show |
3 | a0001c0001t0002g0240a0001c0001t0004g0243a0001c0001t0004g0244 | 3 | HG02572.hp1 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.641+707_641+708ins others(11): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776096 | ||||||
| chr13:31776096
|
CT | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0030others(25): Show | 28 | HG00438.hp1 HG01074.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.641+711delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776096 | |||||
| chr13:31776097
|
T | C | 4 | a0001c0001t0002g0240a0001c0001t0004g0243a0001c0001t0004g0244others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+708T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776097 | ||||||
| chr13:31776097
|
T | TTTC | 3 | a0001c0002t0002g0136a0001c0002t0002g0373a0003c0005t0002g0241 | 3 | HG01175.hp1 HG03209.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.641+710_641+711ins others(3): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776097 | |||||
| chr13:31776097
|
T | TTTCTTCT others(7): Show |
1 | a0001c0001t0001g0358 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.641+710_641+711ins others(14): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776097 | |||||
| chr13:31776101
|
CT | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 25 | HG00609.hp1 HG01243.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.641+716delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776101 | |||||
| chr13:31776102
|
T | C | 2 | a0001c0002t0002g0381a0001c0002t0002g0382 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.641+713T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776102 | ||||||
| chr13:31776102
|
T | TTTC | 50 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0115others(47): Show | 50 | HG00673.hp2 HG00741.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.641+715_641+716ins others(3): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTCTTTC | 41 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0032others(38): Show | 42 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+715_641+716ins others(7): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTCTTTC others(4): Show |
45 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0046others(42): Show | 46 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.641+715_641+716ins others(11): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTCTTTC others(8): Show |
40 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0039others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.641+715_641+716ins others(15): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTCTTTC others(12): Show |
13 | a0001c0001t0001g0036a0001c0001t0001g0114a0001c0001t0001g0171others(10): Show | 13 | HG01081.hp1 HG01934.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.641+715_641+716ins others(19): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTCTTTC others(16): Show |
8 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0179others(5): Show | 8 | HG01943.hp2 HG02698.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.641+715_641+716ins others(23): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTCTTTC others(20): Show |
1 | a0001c0001t0001g0215 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.641+715_641+716ins others(27): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTCTTTC others(24): Show |
1 | a0001c0001t0001g0206 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.641+715_641+716ins others(31): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTTC | 37 | a0001c0002t0002g0003a0001c0002t0002g0005a0001c0002t0002g0093others(34): Show | 38 | HG00438.hp2 HG00609.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.641+751_641+754dup others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTTCTTT others(1): Show |
36 | a0001c0002t0001g0350a0001c0002t0002g0007a0001c0002t0002g0119others(33): Show | 36 | HG00558.hp1 HG01081.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.641+747_641+754dup others(8): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTTCTTT others(5): Show |
14 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0034others(11): Show | 14 | HG00099.hp1 HG00673.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.641+743_641+754dup others(12): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTTCTTT others(9): Show |
5 | a0001c0002t0002g0229a0001c0002t0002g0313a0001c0002t0002g0339others(2): Show | 5 | HG01099.hp2 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.641+739_641+754dup others(16): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTTCTTT others(13): Show |
3 | a0001c0002t0002g0055a0001c0002t0002g0252a0001c0002t0002g0277 | 3 | HG00544.hp2 NA18522.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.641+735_641+754dup others(20): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTTCTTT others(17): Show |
1 | a0001c0002t0002g0279 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.641+731_641+754dup others(24): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
T | TTTTCTTT others(21): Show |
1 | a0001c0002t0002g0278 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.641+727_641+754dup others(28): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776102
|
TTTTC | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(7): Show | 10 | HG01074.hp1 HG01192.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.641+751_641+754del others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776102 | |||||
| chr13:31776103
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.641+714T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776103 | ||||||
| chr13:31776105
|
T | C | 3 | a0001c0002t0002g0380a0003c0005t0002g0105a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03453.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.641+716T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776105 | ||||||
| chr13:31776106
|
C | T | 3 | a0001c0002t0002g0380a0003c0005t0002g0105a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03453.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.641+717C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776106 | ||||||
| chr13:31776107
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.641+718T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776107 | ||||||
| chr13:31776140
|
TTC | T | 3 | a0001c0001t0002g0240a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.641+755_641+756del others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776140 | |||||
| chr13:31776188
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 139 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.641+799T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776188 | ||||||
| chr13:31776253
|
C | CT | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(126): Show | 131 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.641+884dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776253 | |||||
| chr13:31776253
|
C | CTT | 19 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG01175.hp2 HG02300.hp2 HG02738.hp2 others(16): Show |
intron_variant | MODIFIER | c.641+883_641+884dup others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776253 | |||||
| chr13:31776253
|
C | CTTT | 8 | a0001c0001t0001g0030a0001c0001t0001g0145a0001c0001t0002g0004others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+882_641+884dup others(3): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776253 | |||||
| chr13:31776253
|
CT | C | 73 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0003g0098others(70): Show | 73 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.641+884delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr13 | 31776253 | |||||
| chr13:31776420
|
G | A | 2 | a0001c0002t0002g0373a0001c0011t0001g0254 | 2 | HG01175.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.642-956G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776420 | ||||||
| chr13:31776445
|
T | C | 56 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0013t0002g0012others(53): Show | 56 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.642-931T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776445 | ||||||
| chr13:31776483
|
A | G | 13 | a0001c0001t0001g0031a0001c0001t0001g0106a0001c0001t0001g0108others(10): Show | 13 | NA18950.hp1 NA18968.hp2 NA18973.hp1 others(10): Show |
intron_variant | MODIFIER | c.642-893A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776483 | ||||||
| chr13:31776795
|
C | T | 1 | a0001c0002t0002g0315 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.642-581C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776795 | ||||||
| chr13:31776796
|
C | G | 4 | a0001c0002t0002g0136a0001c0002t0002g0380a0001c0002t0002g0381others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-580C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776796 | ||||||
| chr13:31776900
|
C | T | 3 | a0001c0002t0002g0034a0001c0002t0002g0166a0001c0002t0002g0253 | 3 | HG02451.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.642-476C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776900 | ||||||
| chr13:31777025
|
A | C | 95 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(92): Show | 95 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.642-351A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31777025 | ||||||
| chr13:31777104
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.642-272G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31777104 | ||||||
| chr13:31777320
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0237 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.642-56G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31777320 | ||||||
| chr13:31777480
|
C | T | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.713+33C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 8/17 | chr13 | 31777480 | ||||||
| chr13:31777523
|
T | C | 2 | a0001c0002t0002g0373a0001c0011t0001g0254 | 2 | HG01175.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.713+76T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 8/17 | chr13 | 31777523 | ||||||
| chr13:31777692
|
T | A | 2 | a0002c0003t0003g0029a0002c0003t0003g0037 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.713+245T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 8/17 | chr13 | 31777692 | ||||||
| chr13:31778188
|
A | G | 1 | a0001c0001t0005g0194 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.714-324A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 8/17 | chr13 | 31778188 | ||||||
| chr13:31778480
|
T | C | 7 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.714-32T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 8/17 | chr13 | 31778480 | ||||||
| chr13:31778751
|
G | A | 1 | a0001c0002t0002g0307 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.785+168G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31778751 | ||||||
| chr13:31778873
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0237 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.785+290C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31778873 | ||||||
| chr13:31778963
|
C | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(219): Show | 224 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.785+380C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31778963 | ||||||
| chr13:31779122
|
T | TTA | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(253): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.785+540_785+541ins others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr13 | 31779122 | |||||
| chr13:31779124
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG01074.hp2 HG01943.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.785+541G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779124 | ||||||
| chr13:31779126
|
C | CT | 18 | a0001c0001t0001g0114a0001c0001t0002g0017a0001c0001t0002g0100others(15): Show | 18 | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.785+560dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr13 | 31779126 | |||||
| chr13:31779126
|
C | CTT | 38 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(35): Show | 38 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.785+559_785+560dup others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr13 | 31779126 | |||||
| chr13:31779126
|
C | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG01074.hp2 HG01943.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.785+543C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779126 | ||||||
| chr13:31779127
|
T | TC | 6 | a0001c0001t0001g0039a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG01074.hp2 HG01943.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.785+544_785+545ins others(1): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779127 | ||||||
| chr13:31779184
|
G | A | 3 | a0001c0002t0002g0034a0001c0002t0002g0166a0001c0002t0002g0253 | 3 | HG02451.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.785+601G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779184 | ||||||
| chr13:31779482
|
C | T | 2 | a0001c0001t0002g0100a0001c0001t0002g0123 | 2 | HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.785+899C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779482 | ||||||
| chr13:31779502
|
A | T | 56 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0013t0002g0012others(53): Show | 56 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.785+919A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779502 | ||||||
| chr13:31779576
|
G | A | 1 | a0001c0002t0002g0231 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.785+993G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779576 | ||||||
| chr13:31779598
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0192a0001c0001t0001g0267 | 4 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+1015C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779598 | ||||||
| chr13:31779654
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(259): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.785+1071T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779654 | ||||||
| chr13:31779655
|
G | A | 4 | a0001c0001t0001g0260a0001c0001t0001g0262a0001c0001t0001g0268others(1): Show | 4 | HG01081.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+1072G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779655 | ||||||
| chr13:31779764
|
A | G | 2 | a0001c0001t0002g0170a0001c0001t0002g0172 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.785+1181A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779764 | ||||||
| chr13:31779824
|
T | G | 1 | a0001c0002t0002g0380 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.785+1241T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779824 | ||||||
| chr13:31779872
|
G | A | 67 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0002g0004others(64): Show | 67 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.785+1289G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779872 | ||||||
| chr13:31779994
|
A | G | 25 | a0001c0001t0001g0358a0001c0004t0001g0020a0001c0004t0001g0076others(22): Show | 25 | HG00280.hp2 HG00621.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.785+1411A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779994 | ||||||
| chr13:31780078
|
C | T | 1 | a0001c0002t0002g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.785+1495C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780078 | ||||||
| chr13:31780172
|
G | A | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 39 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.786-1499G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780172 | ||||||
| chr13:31780200
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.786-1471C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780200 | ||||||
| chr13:31780222
|
G | A | 1 | a0001c0002t0002g0330 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.786-1449G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780222 | ||||||
| chr13:31780309
|
G | A | 1 | a0002c0003t0003g0083 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.786-1362G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780309 | ||||||
| chr13:31780376
|
CCTT | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(136): Show | 141 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.786-1290_786-1288d others(5): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr13 | 31780376 | |||||
| chr13:31780614
|
C | T | 1 | a0004c0014t0002g0305 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.786-1057C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780614 | ||||||
| chr13:31780738
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0002g0017a0001c0001t0002g0018 | 3 | HG01496.hp1 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.786-933G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780738 | ||||||
| chr13:31780746
|
C | T | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(34): Show | 37 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.786-925C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780746 | ||||||
| chr13:31780898
|
G | A | 1 | a0001c0002t0002g0252 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.786-773G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31780898 | ||||||
| chr13:31781046
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.786-625C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781046 | ||||||
| chr13:31781295
|
T | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.786-376T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781295 | ||||||
| chr13:31781311
|
A | G | 1 | a0001c0002t0002g0375 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786-360A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781311 | ||||||
| chr13:31781334
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.786-337G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781334 | ||||||
| chr13:31781449
|
G | A | 368 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(365): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.786-222G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781449 | ||||||
| chr13:31781479
|
A | C | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.786-192A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781479 | ||||||
| chr13:31781485
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.786-186A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781485 | ||||||
| chr13:31781542
|
T | C | 1 | a0001c0002t0002g0272 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.786-129T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781542 | ||||||
| chr13:31781556
|
G | GC | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.786-115_786-114ins others(1): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781556 | ||||||
| chr13:31781611
|
T | A | 2 | a0002c0003t0003g0029a0002c0003t0003g0037 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.786-60T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31781611 | ||||||
| chr13:31781632
|
C | CA | 14 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(11): Show | 14 | HG01175.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.786-33dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr13 | 31781632 | |||||
| chr13:31781990
|
G | A | 1 | a0001c0002t0002g0307 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.857+248G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 10/17 | chr13 | 31781990 | ||||||
| chr13:31782151
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(215): Show | 220 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.857+409C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 10/17 | chr13 | 31782151 | ||||||
| chr13:31782236
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.858-440C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 10/17 | chr13 | 31782236 | ||||||
| chr13:31782369
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.858-307G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 10/17 | chr13 | 31782369 | ||||||
| chr13:31782627
|
T | G | 1 | a0005c0009t0001g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.858-49T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 10/17 | chr13 | 31782627 | ||||||
| chr13:31782640
|
G | A | 10 | a0001c0004t0001g0020a0001c0004t0001g0076a0001c0004t0001g0077others(7): Show | 10 | HG01346.hp2 NA18959.hp2 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.858-36G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 10/17 | chr13 | 31782640 | ||||||
| chr13:31782760
|
G | T | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.929+13G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31782760 | ||||||
| chr13:31782765
|
C | G | 1 | a0001c0001t0002g0230 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.929+18C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31782765 | ||||||
| chr13:31782910
|
A | T | 1 | a0002c0003t0003g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.929+163A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31782910 | ||||||
| chr13:31782946
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+199A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31782946 | ||||||
| chr13:31782979
|
G | T | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.929+232G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31782979 | ||||||
| chr13:31783206
|
C | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+459C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783206 | ||||||
| chr13:31783221
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+474A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783221 | ||||||
| chr13:31783398
|
T | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+651T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783398 | ||||||
| chr13:31783418
|
T | A | 1 | a0001c0001t0002g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.929+671T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783418 | ||||||
| chr13:31783426
|
A | T | 1 | a0001c0004t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.929+679A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783426 | ||||||
| chr13:31783516
|
T | TAACTC | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+771_929+772ins others(5): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783516 | |||||
| chr13:31783523
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+776A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783523 | ||||||
| chr13:31783579
|
A | C | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.929+832A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783579 | ||||||
| chr13:31783713
|
T | C | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.929+966T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783713 | ||||||
| chr13:31783796
|
TTTTG | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(253): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.929+1065_929+1068d others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783796 | |||||
| chr13:31783808
|
G | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.929+1061G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783808 | ||||||
| chr13:31783961
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+1214T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783961 | ||||||
| chr13:31783981
|
T | A | 1 | a0001c0002t0002g0324 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.929+1234T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783981 | ||||||
| chr13:31783983
|
A | AT | 16 | a0001c0002t0002g0034a0001c0002t0002g0055a0001c0002t0002g0146others(13): Show | 16 | HG00544.hp2 HG02148.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.929+1251dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATT | 61 | a0001c0001t0001g0358a0001c0002t0001g0350a0001c0002t0002g0003others(58): Show | 62 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.929+1250_929+1251d others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATTT | 15 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0002t0002g0092others(12): Show | 15 | HG02040.hp2 HG02132.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.929+1249_929+1251d others(5): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATTTT | 63 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0240others(60): Show | 63 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.929+1248_929+1251d others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATTTTT | 14 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0026others(11): Show | 14 | HG02004.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.929+1247_929+1251d others(7): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATTTTTTT | 10 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0155others(7): Show | 10 | HG00639.hp2 HG01175.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.929+1245_929+1251d others(9): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATTTTTTT others(1): Show |
121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(118): Show | 123 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.929+1244_929+1251d others(10): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATTTTTTT others(2): Show |
44 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 44 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.929+1243_929+1251d others(11): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATTTTTTT others(3): Show |
6 | a0001c0001t0001g0125a0001c0001t0001g0271a0001c0001t0001g0289others(3): Show | 6 | HG00741.hp1 HG01099.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.929+1242_929+1251d others(12): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31783983
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.929+1241_929+1251d others(13): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 31783983 | |||||
| chr13:31784041
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.929+1294G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784041 | ||||||
| chr13:31784074
|
G | A | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.929+1327G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784074 | ||||||
| chr13:31784090
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+1343A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784090 | ||||||
| chr13:31784123
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.929+1376A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784123 | ||||||
| chr13:31784328
|
A | G | 1 | a0001c0011t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.929+1581A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784328 | ||||||
| chr13:31784352
|
C | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | NA18947.hp1 NA18967.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.929+1605C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784352 | ||||||
| chr13:31784391
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.929+1644G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784391 | ||||||
| chr13:31784545
|
T | C | 1 | a0001c0002t0002g0270 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.929+1798T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784545 | ||||||
| chr13:31784601
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.930-1782C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784601 | ||||||
| chr13:31784809
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.930-1574G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784809 | ||||||
| chr13:31784813
|
C | T | 3 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0230 | 3 | HG01496.hp1 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.930-1570C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784813 | ||||||
| chr13:31784930
|
C | A | 65 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(62): Show | 65 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.930-1453C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784930 | ||||||
| chr13:31784930
|
C | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(189): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.930-1453C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784930 | ||||||
| chr13:31784991
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.930-1392C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784991 | ||||||
| chr13:31785055
|
G | A | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 39 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.930-1328G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785055 | ||||||
| chr13:31785088
|
G | A | 67 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(64): Show | 67 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.930-1295G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785088 | ||||||
| chr13:31785267
|
C | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.930-1116C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785267 | ||||||
| chr13:31785319
|
G | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.930-1064G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785319 | ||||||
| chr13:31785439
|
T | C | 4 | a0001c0002t0002g0363a0001c0002t0002g0364a0001c0002t0002g0365others(1): Show | 4 | HG02280.hp1 HG03209.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.930-944T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785439 | ||||||
| chr13:31785500
|
T | G | 1 | a0001c0002t0002g0307 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.930-883T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785500 | ||||||
| chr13:31785641
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(138): Show | 143 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.930-742A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785641 | ||||||
| chr13:31785749
|
A | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(138): Show | 143 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.930-634A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785749 | ||||||
| chr13:31785823
|
T | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.930-560T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785823 | ||||||
| chr13:31785824
|
G | A | 1 | a0001c0002t0002g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.930-559G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785824 | ||||||
| chr13:31785971
|
C | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.930-412C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785971 | ||||||
| chr13:31786005
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.930-378G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31786005 | ||||||
| chr13:31786028
|
C | T | 14 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG03017.hp2 HG03654.hp2 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.930-355C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31786028 | ||||||
| chr13:31786092
|
G | A | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.930-291G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31786092 | ||||||
| chr13:31786142
|
T | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.930-241T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31786142 | ||||||
| chr13:31786212
|
C | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.930-171C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31786212 | ||||||
| chr13:31786221
|
T | C | 4 | a0001c0002t0002g0346a0001c0002t0002g0347a0001c0002t0002g0348others(1): Show | 4 | NA18966.hp2 NA18967.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.930-162T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31786221 | ||||||
| chr13:31786263
|
T | C | 1 | a0001c0002t0002g0301 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.930-120T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31786263 | ||||||
| chr13:31786483
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1001+29T>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 12/17 | chr13 | 31786483 | ||||||
| chr13:31786525
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1002-41C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 12/17 | chr13 | 31786525 | ||||||
| chr13:31786554
|
T | TA | 53 | a0001c0013t0002g0012a0002c0003t0003g0021a0002c0003t0003g0022others(50): Show | 53 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(50): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1002-2dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 31786554 | |||||
| chr13:31786554
|
T | TAA | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1002-3_1002-2dupAA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 31786554 | |||||
| chr13:31786554
|
T | TAAA | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(101): Show | 104 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1002-4_1002-2dupAA others(1): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 31786554 | |||||
| chr13:31786786
|
CAAAT | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1073+152_1073+155d others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 31786786 | |||||
| chr13:31786995
|
C | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1073+358C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31786995 | ||||||
| chr13:31787027
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+390A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787027 | ||||||
| chr13:31787189
|
A | G | 1 | a0001c0002t0002g0156 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1073+552A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787189 | ||||||
| chr13:31787367
|
A | T | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245 | 3 | HG02572.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1073+730A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787367 | ||||||
| chr13:31787522
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1073+885T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787522 | ||||||
| chr13:31787678
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1073+1041C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787678 | ||||||
| chr13:31787688
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1073+1051A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787688 | ||||||
| chr13:31787784
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0184 | 2 | NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1073+1147C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787784 | ||||||
| chr13:31787792
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1073+1155G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787792 | ||||||
| chr13:31787920
|
C | T | 1 | a0009c0006t0001g0258 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1074-1202C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31787920 | ||||||
| chr13:31788033
|
G | A | 11 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1074-1089G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31788033 | ||||||
| chr13:31788065
|
T | C | 1 | a0002c0003t0003g0069 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1074-1057T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31788065 | ||||||
| chr13:31788072
|
G | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1074-1050G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31788072 | ||||||
| chr13:31788131
|
C | T | 1 | a0001c0002t0006g0314 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1074-991C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31788131 | ||||||
| chr13:31788137
|
G | GA | 27 | a0001c0002t0002g0007a0001c0002t0002g0013a0001c0002t0002g0014others(24): Show | 27 | HG00544.hp2 HG01175.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1074-972dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 31788137 | |||||
| chr13:31788137
|
G | GAA | 90 | a0001c0002t0001g0350a0001c0002t0002g0003a0001c0002t0002g0005others(87): Show | 91 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1074-973_1074-972d others(4): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 31788137 | |||||
| chr13:31788137
|
GA | G | 8 | a0001c0001t0001g0188a0001c0001t0001g0222a0001c0001t0002g0230others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074-972delA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 31788137 | |||||
| chr13:31788139
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1074-983A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31788139 | ||||||
| chr13:31788417
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(254): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1074-705A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31788417 | ||||||
| chr13:31788473
|
A | G | 1 | a0001c0002t0002g0309 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1074-649A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31788473 | ||||||
| chr13:31788770
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0222 | 2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1074-352A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31788770 | ||||||
| chr13:31789073
|
TAA | T | 12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.1074-46_1074-45del others(2): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 31789073 | |||||
| chr13:31789080
|
T | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG03017.hp2 HG03654.hp2 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074-42T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 13/17 | chr13 | 31789080 | ||||||
| chr13:31789201
|
T | C | 7 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(4): Show | 7 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1145+8T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31789201 | ||||||
| chr13:31789233
|
A | T | 12 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(9): Show | 12 | HG01496.hp1 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1145+40A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31789233 | ||||||
| chr13:31789506
|
C | T | 1 | a0001c0002t0002g0317 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1145+313C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31789506 | ||||||
| chr13:31789536
|
G | A | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1145+343G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31789536 | ||||||
| chr13:31789821
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1145+628A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31789821 | ||||||
| chr13:31789968
|
A | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0163others(4): Show | 7 | HG01255.hp1 HG01975.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145+775A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31789968 | ||||||
| chr13:31790033
|
G | T | 1 | a0001c0001t0004g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1145+840G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790033 | ||||||
| chr13:31790200
|
G | A | 1 | a0001c0013t0002g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1145+1007G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790200 | ||||||
| chr13:31790364
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1145+1171C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790364 | ||||||
| chr13:31790454
|
C | T | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245 | 3 | HG02572.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1145+1261C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790454 | ||||||
| chr13:31790560
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0172 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1146-1246C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790560 | ||||||
| chr13:31790574
|
C | G | 4 | a0001c0002t0002g0034a0001c0002t0002g0166a0001c0002t0002g0253others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146-1232C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790574 | ||||||
| chr13:31790575
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1146-1231G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790575 | ||||||
| chr13:31790694
|
C | T | 91 | a0001c0002t0001g0350a0001c0002t0002g0003a0001c0002t0002g0005others(88): Show | 92 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1146-1112C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790694 | ||||||
| chr13:31790704
|
T | C | 13 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0003g0098others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1146-1102T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790704 | ||||||
| chr13:31790817
|
T | TC | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(34): Show | 37 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1146-989_1146-988i others(3): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790817 | ||||||
| chr13:31790847
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1146-959C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790847 | ||||||
| chr13:31790851
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1146-955G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31790851 | ||||||
| chr13:31791059
|
A | G | 1 | a0001c0013t0002g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1146-747A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791059 | ||||||
| chr13:31791098
|
G | A | 3 | a0001c0002t0001g0350a0001c0002t0002g0306a0001c0002t0002g0327 | 3 | HG01081.hp2 HG01346.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1146-708G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791098 | ||||||
| chr13:31791109
|
A | C | 1 | a0001c0001t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1146-697A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791109 | ||||||
| chr13:31791134
|
A | G | 91 | a0001c0002t0001g0350a0001c0002t0002g0003a0001c0002t0002g0005others(88): Show | 92 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1146-672A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791134 | ||||||
| chr13:31791151
|
C | G | 1 | a0001c0001t0002g0004 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1146-655C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791151 | ||||||
| chr13:31791374
|
A | G | 1 | a0001c0002t0002g0304 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1146-432A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791374 | ||||||
| chr13:31791545
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045 | 3 | NA18974.hp2 NA18991.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1146-261T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791545 | ||||||
| chr13:31791578
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1146-228T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791578 | ||||||
| chr13:31791672
|
A | G | 14 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0003g0098others(11): Show | 14 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1146-134A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 14/17 | chr13 | 31791672 | ||||||
| chr13:31792124
|
A | G | 1 | a0001c0002t0002g0357 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1375+89A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 15/17 | chr13 | 31792124 | ||||||
| chr13:31792154
|
G | T | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1375+119G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 15/17 | chr13 | 31792154 | ||||||
| chr13:31792162
|
T | C | 14 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0003g0098others(11): Show | 14 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1375+127T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 15/17 | chr13 | 31792162 | ||||||
| chr13:31792253
|
A | G | 14 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0003g0098others(11): Show | 14 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1375+218A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 15/17 | chr13 | 31792253 | ||||||
| chr13:31792334
|
C | T | 1 | a0001c0002t0002g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1375+299C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 15/17 | chr13 | 31792334 | ||||||
| chr13:31793184
|
A | G | 1 | a0001c0001t0004g0243 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1786+96A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31793184 | ||||||
| chr13:31793222
|
A | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1786+134A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31793222 | ||||||
| chr13:31793431
|
C | CT | 123 | a0001c0001t0001g0237a0001c0001t0002g0004a0001c0001t0002g0025others(120): Show | 124 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1786+357dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31793431 | |||||
| chr13:31793431
|
CT | C | 7 | a0001c0001t0005g0203a0001c0002t0002g0013a0001c0002t0002g0014others(4): Show | 7 | HG02896.hp1 HG02897.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1786+357delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31793431 | |||||
| chr13:31793788
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1786+700A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31793788 | ||||||
| chr13:31793830
|
C | T | 2 | a0001c0002t0002g0381a0001c0002t0002g0382 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1786+742C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31793830 | ||||||
| chr13:31793833
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1786+745T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31793833 | ||||||
| chr13:31794282
|
G | C | 90 | a0001c0002t0001g0350a0001c0002t0002g0003a0001c0002t0002g0005others(87): Show | 91 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1786+1194G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794282 | ||||||
| chr13:31794352
|
C | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0137a0001c0001t0001g0155others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+1264C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794352 | ||||||
| chr13:31794368
|
C | CCA | 10 | a0001c0001t0004g0238a0001c0002t0002g0013a0001c0002t0002g0014others(7): Show | 10 | HG00544.hp2 HG01243.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1786+1320_1786+132 others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31794368 | |||||
| chr13:31794368
|
C | CCACA | 4 | a0001c0001t0004g0016a0001c0002t0002g0007a0001c0002t0002g0249others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+1318_1786+132 others(8): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31794368 | |||||
| chr13:31794368
|
CCA | C | 10 | a0001c0002t0002g0136a0001c0002t0002g0251a0001c0002t0002g0270others(7): Show | 10 | HG00741.hp2 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1786+1320_1786+132 others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31794368 | |||||
| chr13:31794368
|
CCACA | C | 62 | a0001c0001t0001g0019a0001c0001t0001g0137a0001c0001t0002g0100others(59): Show | 62 | HG00099.hp1 HG00609.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1786+1318_1786+132 others(8): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31794368 | |||||
| chr13:31794368
|
CCACACA | C | 94 | a0001c0001t0001g0042a0001c0001t0001g0086a0001c0001t0001g0175others(91): Show | 95 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1786+1316_1786+132 others(10): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31794368 | |||||
| chr13:31794368
|
CCACACAC others(1): Show |
C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1786+1314_1786+132 others(12): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31794368 | |||||
| chr13:31794368
|
CCACACAC others(3): Show |
C | 6 | a0001c0001t0001g0115a0001c0001t0001g0197a0001c0002t0002g0119others(3): Show | 6 | HG02886.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786+1312_1786+132 others(14): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31794368 | |||||
| chr13:31794368
|
CCACACAC others(5): Show |
C | 14 | a0001c0001t0001g0031a0001c0001t0001g0106a0001c0001t0001g0108others(11): Show | 14 | HG02109.hp1 HG03041.hp1 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.1786+1310_1786+132 others(16): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31794368 | |||||
| chr13:31794394
|
A | G | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245 | 3 | HG02572.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1786+1306A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794394 | ||||||
| chr13:31794427
|
A | C | 14 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0003g0098others(11): Show | 14 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1786+1339A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794427 | ||||||
| chr13:31794484
|
C | T | 5 | a0001c0001t0004g0016a0001c0001t0004g0238a0001c0002t0002g0034others(2): Show | 5 | HG02145.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+1396C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794484 | ||||||
| chr13:31794505
|
C | G | 1 | a0001c0011t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1786+1417C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794505 | ||||||
| chr13:31794523
|
C | A | 3 | a0002c0003t0003g0028a0002c0003t0003g0089a0002c0003t0003g0090 | 3 | HG02572.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1786+1435C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794523 | ||||||
| chr13:31794669
|
G | T | 1 | a0002c0003t0003g0104 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1786+1581G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794669 | ||||||
| chr13:31794836
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG03017.hp2 HG03654.hp2 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.1786+1748G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794836 | ||||||
| chr13:31794946
|
A | T | 1 | a0002c0003t0003g0064 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1786+1858A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31794946 | ||||||
| chr13:31795144
|
G | C | 12 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(9): Show | 12 | HG01496.hp1 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1786+2056G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795144 | ||||||
| chr13:31795178
|
C | T | 2 | a0001c0002t0002g0272a0001c0002t0002g0274 | 2 | NA19080.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1787-2023C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795178 | ||||||
| chr13:31795210
|
C | T | 52 | a0002c0003t0003g0021a0002c0003t0003g0022a0002c0003t0003g0023others(49): Show | 52 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1787-1991C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795210 | ||||||
| chr13:31795262
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG03017.hp2 HG03654.hp2 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.1787-1939G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795262 | ||||||
| chr13:31795312
|
G | A | 1 | a0001c0002t0002g0383 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1787-1889G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795312 | ||||||
| chr13:31795627
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1787-1574G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795627 | ||||||
| chr13:31795723
|
A | AT | 3 | a0001c0001t0001g0002a0001c0001t0001g0192a0001c0001t0001g0267 | 4 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1472dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31795723 | |||||
| chr13:31795800
|
G | A | 1 | a0001c0015t0003g0376 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1787-1401G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795800 | ||||||
| chr13:31795845
|
G | A | 4 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(1): Show | 4 | HG02145.hp2 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1356G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795845 | ||||||
| chr13:31795903
|
C | A | 52 | a0002c0003t0003g0021a0002c0003t0003g0022a0002c0003t0003g0023others(49): Show | 52 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1787-1298C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795903 | ||||||
| chr13:31796038
|
C | CT | 28 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(25): Show | 28 | HG00438.hp2 HG01175.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.1787-1134dupT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31796038 | |||||
| chr13:31796038
|
CT | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(182): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1787-1134delT | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31796038 | |||||
| chr13:31796038
|
CTT | C | 40 | a0001c0001t0001g0161a0001c0001t0001g0183a0001c0001t0001g0202others(37): Show | 40 | HG00438.hp1 HG00673.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1787-1135_1787-113 others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31796038 | |||||
| chr13:31796038
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245 | 3 | HG02572.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1787-1143_1787-113 others(14): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31796038 | |||||
| chr13:31796163
|
C | G | 90 | a0001c0002t0001g0350a0001c0002t0002g0003a0001c0002t0002g0005others(87): Show | 91 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1787-1038C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796163 | ||||||
| chr13:31796207
|
G | A | 1 | a0003c0005t0002g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1787-994G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796207 | ||||||
| chr13:31796239
|
C | T | 2 | a0001c0002t0002g0299a0001c0002t0002g0302 | 2 | HG01255.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1787-962C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796239 | ||||||
| chr13:31796241
|
G | T | 10 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1787-960G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796241 | ||||||
| chr13:31796360
|
C | T | 1 | a0001c0002t0002g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1787-841C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796360 | ||||||
| chr13:31796453
|
A | G | 10 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1787-748A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796453 | ||||||
| chr13:31796488
|
T | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0237 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1787-713T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796488 | ||||||
| chr13:31796523
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(239): Show | 244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1787-678C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796523 | ||||||
| chr13:31796624
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0267 | 3 | HG00280.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1787-577C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796624 | ||||||
| chr13:31796632
|
G | A | 2 | a0002c0003t0003g0029a0002c0003t0003g0037 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1787-569G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796632 | ||||||
| chr13:31796796
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1787-405A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796796 | ||||||
| chr13:31796943
|
A | C | 1 | a0001c0002t0002g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1787-258A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31796943 | ||||||
| chr13:31797072
|
TTCCGAAA | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0237a0001c0001t0003g0098others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-118_1787-112d others(9): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 31797072 | |||||
| chr13:31797428
|
C | A | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2005+9C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31797428 | ||||||
| chr13:31797514
|
T | C | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(345): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.2005+95T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31797514 | ||||||
| chr13:31797570
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0237a0001c0001t0003g0098others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2005+151A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31797570 | ||||||
| chr13:31797726
|
C | G | 1 | a0001c0001t0005g0194 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2005+307C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31797726 | ||||||
| chr13:31797849
|
A | G | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2005+430A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31797849 | ||||||
| chr13:31797877
|
C | T | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(34): Show | 37 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.2005+458C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31797877 | ||||||
| chr13:31798014
|
A | G | 1 | a0001c0002t0002g0255 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2005+595A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798014 | ||||||
| chr13:31798202
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2005+783A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798202 | ||||||
| chr13:31798231
|
C | T | 14 | a0001c0001t0001g0031a0001c0001t0001g0106a0001c0001t0001g0108others(11): Show | 14 | NA18950.hp1 NA18968.hp2 NA18973.hp1 others(11): Show |
intron_variant | MODIFIER | c.2005+812C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798231 | ||||||
| chr13:31798253
|
C | T | 10 | a0001c0001t0002g0100a0001c0001t0002g0123a0001c0001t0004g0016others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2005+834C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798253 | ||||||
| chr13:31798360
|
G | C | 3 | a0001c0002t0002g0034a0001c0002t0002g0166a0001c0002t0002g0253 | 3 | HG02451.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2005+941G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798360 | ||||||
| chr13:31798549
|
A | G | 1 | a0001c0002t0002g0325 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2005+1130A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798549 | ||||||
| chr13:31798707
|
A | T | 1 | a0001c0002t0002g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2005+1288A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798707 | ||||||
| chr13:31798774
|
C | A | 1 | a0001c0011t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2005+1355C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798774 | ||||||
| chr13:31798832
|
G | C | 365 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(362): Show | 368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.2005+1413G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798832 | ||||||
| chr13:31798836
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2005+1417T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798836 | ||||||
| chr13:31798952
|
A | G | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(34): Show | 37 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.2005+1533A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798952 | ||||||
| chr13:31798978
|
T | C | 47 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(44): Show | 47 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2005+1559T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31798978 | ||||||
| chr13:31799059
|
C | A | 1 | a0001c0001t0005g0152 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2005+1640C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799059 | ||||||
| chr13:31799163
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(136): Show | 141 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.2005+1744G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799163 | ||||||
| chr13:31799219
|
C | CA | 9 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0002t0002g0277others(6): Show | 9 | HG02027.hp2 HG02886.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.2005+1814dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 31799219 | |||||
| chr13:31799219
|
CA | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 138 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.2005+1814delA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 31799219 | |||||
| chr13:31799456
|
C | A | 1 | a0001c0002t0002g0325 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2005+2037C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799456 | ||||||
| chr13:31799489
|
A | C | 1 | a0001c0001t0002g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2005+2070A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799489 | ||||||
| chr13:31799553
|
G | T | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2005+2134G>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799553 | ||||||
| chr13:31799606
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2005+2187G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799606 | ||||||
| chr13:31799764
|
A | G | 3 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0015t0003g0376 | 3 | HG01243.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2005+2345A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799764 | ||||||
| chr13:31799777
|
A | G | 2 | a0002c0003t0003g0048a0002c0003t0003g0066 | 2 | NA18942.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2005+2358A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799777 | ||||||
| chr13:31799805
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 139 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.2006-2341C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799805 | ||||||
| chr13:31799872
|
G | A | 1 | a0001c0011t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2006-2274G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799872 | ||||||
| chr13:31799891
|
T | C | 3 | a0001c0002t0002g0034a0001c0002t0002g0166a0001c0002t0002g0253 | 3 | HG02451.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2006-2255T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799891 | ||||||
| chr13:31799916
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2006-2230C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799916 | ||||||
| chr13:31799928
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2006-2218A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31799928 | ||||||
| chr13:31800104
|
G | A | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2006-2042G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800104 | ||||||
| chr13:31800144
|
G | A | 90 | a0001c0002t0002g0003a0001c0002t0002g0005a0001c0002t0002g0092others(87): Show | 91 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2006-2002G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800144 | ||||||
| chr13:31800184
|
G | A | 55 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0015t0003g0376others(52): Show | 55 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.2006-1962G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800184 | ||||||
| chr13:31800386
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2006-1760C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800386 | ||||||
| chr13:31800417
|
A | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0183a0001c0001t0001g0186 | 3 | HG00558.hp2 HG01934.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.2006-1729A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800417 | ||||||
| chr13:31800427
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2006-1719C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800427 | ||||||
| chr13:31800429
|
G | A | 1 | a0001c0004t0001g0129 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2006-1717G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800429 | ||||||
| chr13:31800430
|
G | A | 3 | a0003c0005t0002g0105a0003c0005t0002g0241a0003c0005t0002g0242 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2006-1716G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800430 | ||||||
| chr13:31800489
|
A | G | 8 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0018others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2006-1657A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800489 | ||||||
| chr13:31800504
|
A | G | 1 | a0001c0004t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2006-1642A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800504 | ||||||
| chr13:31800558
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2006-1588T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800558 | ||||||
| chr13:31800651
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2006-1495G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800651 | ||||||
| chr13:31800839
|
A | ATT | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(239): Show | 244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2006-1301_2006-130 others(6): Show |
RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 31800839 | |||||
| chr13:31800847
|
A | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(240): Show | 245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2006-1299A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800847 | ||||||
| chr13:31801017
|
G | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(146): Show | 151 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.2006-1129G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801017 | ||||||
| chr13:31801230
|
G | A | 1 | a0001c0004t0001g0076 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2006-916G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801230 | ||||||
| chr13:31801316
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(136): Show | 141 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.2006-830C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801316 | ||||||
| chr13:31801344
|
C | T | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 45 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2006-802C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801344 | ||||||
| chr13:31801450
|
G | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(34): Show | 37 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.2006-696G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801450 | ||||||
| chr13:31801461
|
C | A | 2 | a0001c0002t0002g0034a0001c0002t0002g0253 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2006-685C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801461 | ||||||
| chr13:31801475
|
A | C | 3 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0015t0003g0376 | 3 | HG01243.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2006-671A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801475 | ||||||
| chr13:31801617
|
A | T | 1 | a0001c0001t0001g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2006-529A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801617 | ||||||
| chr13:31801652
|
C | G | 1 | a0001c0002t0002g0301 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2006-494C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801652 | ||||||
| chr13:31801691
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2006-455C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801691 | ||||||
| chr13:31801703
|
G | C | 1 | a0001c0002t0002g0325 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2006-443G>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801703 | ||||||
| chr13:31801704
|
C | G | 1 | a0001c0002t0002g0325 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2006-442C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801704 | ||||||
| chr13:31801777
|
G | A | 6 | a0002c0003t0003g0049a0002c0003t0003g0050a0002c0003t0003g0051others(3): Show | 6 | HG00609.hp1 HG02027.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.2006-369G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801777 | ||||||
| chr13:31801787
|
C | A | 1 | a0001c0001t0001g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2006-359C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31801787 | ||||||
| chr13:31801856
|
G | GA | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 139 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.2006-284dupA | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 31801856 | |||||
| chr13:31802020
|
G | A | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0245 | 3 | HG02572.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2006-126G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31802020 |