Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| a0002 | 0/0 | 754 | 52 | 6 | 8 | 36 | 2 | 0 | 27 | RXFP2_chr13_31734526_31808389 | RXFP2 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| a0003 | 0/0 | 754 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| a0004 | 0/0 | 754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| a0005 | 0/0 | 754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| a0006 | 0/0 | 754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| a0007 | 0/0 | 754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| a0008 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| a0009 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | MIVFL others(749): Show |
chr13 | 31734526 | 31808389 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2262 | 173 | 41 | 27 | 82 | 2 | 20 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0001c0002 | 1/0 | 2262 | 126 | 38 | 20 | 50 | 2 | 15 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0001c0004 | 0/0 | 2262 | 23 | 0 | 0 | 20 | 2 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0001c0011 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0001c0013 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0001c0015 | 0/0 | 2262 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0002c0003 | 0/0 | 2262 | 51 | 5 | 8 | 36 | 2 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0002c0012 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0003c0005 | 0/0 | 2262 | 3 | 3 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0004c0006 | 0/0 | 2262 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0005c0008 | 0/0 | 2262 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0006c0009 | 0/0 | 2262 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0007c0010 | 0/0 | 2262 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0008c0007 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
chr13 | 31734526 | 31808389 | ||
| a0009c0014 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | ATGAT others(2257): Show |
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 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0001t0002 | 0/0 | 3336 | 15 | 14 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0001t0003 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0001t0004 | 0/0 | 3336 | 5 | 5 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0001t0005 | 0/0 | 3336 | 3 | 0 | 0 | 3 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0001t0008 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0002t0001 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0002t0002 | 1/0 | 3336 | 122 | 38 | 19 | 49 | 2 | 13 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0002t0006 | 0/0 | 3336 | 2 | 0 | 0 | 0 | 0 | 2 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0002t0007 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0004t0001 | 0/0 | 3336 | 23 | 0 | 0 | 20 | 2 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0011t0001 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0013t0002 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0001c0015t0003 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0002c0003t0003 | 0/0 | 3336 | 51 | 5 | 8 | 36 | 2 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0002c0012t0002 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0003c0005t0002 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0004c0006t0001 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0005c0008t0001 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0006c0009t0001 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0007c0010t0001 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0008c0007t0003 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| a0009c0014t0002 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | AGAAC others(3331): Show |
chr13 | 31734526 | 31808389 |
| actghapid | grch38/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 | 0 | 2 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0048 | 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 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0174 | 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 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | 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 |
| 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 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0194 | 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 |
| a0001c0001t0001g0203 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0234 | 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 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0009 | 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 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0002g0248 | 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 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0271 | 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 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0276 | 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 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0329 | 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 | 1 | 0 | 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 |
| a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0350 | 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 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0002g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0006g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0006g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0002t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0022 | 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 |
| a0001c0004t0001g0081 | 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 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0011t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0013t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0001c0015t0003g0374 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0002c0003t0003g0055 | 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 |
| a0002c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0077 | 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 |
| a0002c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0003t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0003t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0002c0012t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0003c0005t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0003c0005t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0003c0005t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0004c0006t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0005c0008t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0006c0009t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0007c0010t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0008c0007t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| a0009c0014t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0295 | 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 | g0265 | EUR | FIN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0124 | EUR | FIN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00438 | hp1 | a0002 | c0003 | t0003 | g0087 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0305 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0332 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00609 | hp1 | a0002 | c0003 | t0003 | g0054 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0281 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0381 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0333 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00673 | hp2 | a0002 | c0003 | t0003 | g0059 | EAS | CHS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0067 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0302 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01071 | hp2 | a0004 | c0006 | t0001 | g0256 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0358 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01074 | hp2 | a0002 | c0003 | t0003 | g0106 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0325 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0311 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0376 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01167 | hp1 | a0002 | c0003 | t0003 | g0063 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0371 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0359 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01243 | hp1 | a0001 | c0015 | t0003 | g0374 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0297 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0308 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0357 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0304 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01346 | hp2 | a0005 | c0008 | t0001 | g0083 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0318 | 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 | g0313 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01433 | hp2 | a0002 | c0003 | t0003 | g0031 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | CLM | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01515 | hp1 | a0002 | c0003 | t0003 | g0046 | EUR | IBS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0298 | EUR | IBS | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0348 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0296 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0320 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02004 | hp2 | a0002 | c0003 | t0003 | g0072 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02015 | hp1 | a0002 | c0003 | t0003 | g0122 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0051 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0097 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0218 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02074 | hp1 | a0002 | c0003 | t0003 | g0075 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0330 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0372 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02132 | hp2 | a0001 | c0004 | t0001 | g0279 | EAS | KHV | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0338 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02148 | hp2 | a0002 | c0003 | t0003 | g0060 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02155 | hp1 | a0002 | c0003 | t0003 | g0053 | EAS | CDX | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0278 | EAS | CDX | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0235 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0249 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02273 | hp2 | a0002 | c0003 | t0003 | g0065 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0363 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0334 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0251 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02451 | hp2 | a0001 | c0013 | t0002 | g0014 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02572 | hp2 | a0002 | c0003 | t0003 | g0092 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0367 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0248 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02647 | hp1 | a0002 | c0003 | t0003 | g0093 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0283 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0314 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0271 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02735 | hp1 | a0006 | c0009 | t0001 | g0163 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0300 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02886 | hp1 | a0003 | c0005 | t0002 | g0229 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0268 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0380 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0379 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0143 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0135 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0043 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02976 | hp1 | a0002 | c0003 | t0003 | g0030 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0366 | AFR | GWD | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0247 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03130 | hp1 | a0002 | c0012 | t0002 | g0113 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0375 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0377 | AFR | ESN | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03209 | hp1 | a0003 | c0005 | t0002 | g0228 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0362 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0155 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0216 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03453 | hp2 | a0003 | c0005 | t0002 | g0107 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0284 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0145 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03688 | hp1 | a0007 | c0010 | t0001 | g0049 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0324 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03704 | hp1 | a0001 | c0002 | t0006 | g0312 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0355 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0286 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03927 | hp1 | a0001 | c0002 | t0006 | g0336 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0337 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0306 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0321 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0127 | SAS | STU | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0361 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | CHB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0025 | EAS | CHB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0352 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18942 | hp2 | a0002 | c0003 | t0003 | g0070 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0204 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0322 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18946 | hp2 | a0002 | c0003 | t0003 | g0066 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18948 | hp1 | a0002 | c0003 | t0003 | g0061 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18949 | hp1 | a0002 | c0003 | t0003 | g0085 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0115 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18951 | hp2 | a0002 | c0003 | t0003 | g0055 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18952 | hp2 | a0002 | c0003 | t0003 | g0058 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18954 | hp2 | a0002 | c0003 | t0003 | g0071 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18956 | hp1 | a0002 | c0003 | t0003 | g0062 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18959 | hp1 | a0002 | c0003 | t0003 | g0069 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18959 | hp2 | a0001 | c0004 | t0001 | g0078 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0340 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18964 | hp2 | a0008 | c0007 | t0003 | g0064 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18966 | hp1 | a0002 | c0003 | t0003 | g0056 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0345 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0344 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18968 | hp1 | a0002 | c0003 | t0003 | g0050 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18970 | hp1 | a0002 | c0003 | t0003 | g0285 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0116 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18974 | hp1 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18978 | hp2 | a0002 | c0003 | t0003 | g0052 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0378 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0084 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18981 | hp1 | a0001 | c0004 | t0001 | g0120 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18983 | hp1 | a0001 | c0004 | t0001 | g0117 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0343 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0335 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18987 | hp1 | a0002 | c0003 | t0003 | g0368 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18988 | hp2 | a0001 | c0002 | t0007 | g0327 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0360 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18990 | hp1 | a0001 | c0004 | t0001 | g0022 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18994 | hp1 | a0002 | c0003 | t0003 | g0076 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0341 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19001 | hp1 | a0002 | c0003 | t0003 | g0068 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19002 | hp2 | a0001 | c0004 | t0001 | g0079 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19003 | hp1 | a0009 | c0014 | t0002 | g0303 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19005 | hp2 | a0001 | c0004 | t0001 | g0121 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0082 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19009 | hp2 | a0002 | c0003 | t0003 | g0221 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19011 | hp1 | a0002 | c0003 | t0003 | g0210 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19012 | hp1 | a0002 | c0003 | t0003 | g0220 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0354 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19064 | hp1 | a0002 | c0003 | t0003 | g0077 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19065 | hp1 | a0002 | c0003 | t0003 | g0369 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0347 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0280 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0080 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19074 | hp1 | a0001 | c0004 | t0001 | g0119 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19080 | hp1 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19081 | hp1 | a0002 | c0003 | t0003 | g0096 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0291 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0350 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19083 | hp2 | a0002 | c0003 | t0003 | g0074 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19084 | hp1 | a0001 | c0004 | t0001 | g0081 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19086 | hp2 | a0002 | c0003 | t0003 | g0026 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0346 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19091 | hp2 | a0002 | c0003 | t0003 | g0073 | EAS | JPT | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0147 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0091 | AFR | YRI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | ASW | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20752 | hp1 | a0002 | c0003 | t0003 | g0104 | EUR | TSI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20752 | hp2 | a0001 | c0004 | t0001 | g0123 | EUR | TSI | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0282 | SAS | GIH | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02109 | hp1 | a0001 | c0011 | t0001 | g0252 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0108 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0212 | AFR | MSL | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0364 | AFR | USA | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | USA | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | USA | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0373 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0181 | REF | REF | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0099 | REF | REF | RXFP2_chr13_31734526_31808389 | RXFP2 | chr13 | 31734526 | 31808389 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31758347 | G | A | 1 | a0004 | 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 | a0009 | 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 | a0005 | 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 | a0006 | 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 | a0007 | 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 | a0002 a0008 |
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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31761743 | G | A | 2 | a0001c0004 a0005c0008 |
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 | a0001c0001 a0001c0004 a0001c0011 others(10): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0013 a0002c0003 a0008c0007 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31802581 | A | G | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(11): Show |
234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): 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 | a0001c0001t0003 a0001c0015t0003 a0002c0003t0003 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31739756 | C | T | 1 | a0001c0002t0002g0381 | 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 | a0001c0002t0002g0373 a0001c0002t0002g0377 a0001c0002t0002g0378 others(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 | a0001c0001t0002g0006 | 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 | a0001c0002t0002g0007 | 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 | a0001c0002t0002g0371 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0254 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0254 a0001c0001t0001g0255 others(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 | a0001c0002t0002g0379 a0001c0002t0002g0380 |
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 | a0001c0001t0001g0246 | 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 | a0001c0002t0002g0247 a0001c0002t0002g0248 a0001c0002t0002g0249 others(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 | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
147 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(144): 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 | a0001c0001t0001g0004 a0001c0001t0001g0254 a0001c0001t0001g0255 others(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 | a0001c0002t0002g0373 a0001c0002t0002g0377 a0001c0011t0001g0252 others(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 | 12 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0236 others(9): 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 | a0003c0005t0002g0107 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0109 a0001c0001t0002g0110 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0002c0003t0003g0104 others(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 | a0001c0001t0001g0114 a0001c0002t0002g0125 a0001c0004t0001g0115 others(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 | a0001c0002t0002g0253 | 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 | a0001c0002t0002g0378 a0001c0002t0002g0379 a0001c0002t0002g0380 |
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 | a0001c0001t0001g0126 | 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 | a0001c0001t0002g0102 a0001c0001t0003g0100 a0001c0001t0003g0101 |
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 | 11 | a0001c0001t0001g0003 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): 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 | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.94+3036G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31742742 | |||||||
| chr13:31742801 | G | A | 376 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(373): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.94+3095G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31742801 | |||||||
| chr13:31742840 | A | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.94+3134A>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31742840 | |||||||
| chr13:31742880 | C | CA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(125): 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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
130 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(127): 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 | a0001c0001t0004g0232 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0273 a0001c0001t0001g0274 others(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 | a0001c0001t0001g0223 | 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 | a0002c0003t0003g0368 a0002c0003t0003g0369 |
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 | a0002c0003t0003g0096 | 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 | a0001c0001t0001g0269 a0001c0002t0002g0247 a0001c0002t0002g0248 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0114 a0001c0002t0002g0125 a0001c0004t0001g0115 others(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 | a0001c0001t0004g0230 | 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 | a0001c0001t0002g0227 | 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 | a0001c0001t0001g0021 a0001c0001t0002g0226 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0365 a0001c0002t0002g0361 a0001c0002t0002g0362 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0365 a0001c0002t0002g0366 a0001c0002t0002g0367 |
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 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0004g0225 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0021 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0379 a0001c0002t0002g0380 |
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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
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 | a0001c0001t0004g0225 | 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 | a0002c0003t0003g0087 | 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 | a0001c0001t0001g0021 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0287 a0001c0001t0001g0288 others(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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): 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 | a0002c0003t0003g0096 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0125 | 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 | 375 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(372): Show |
380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): 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 | a0001c0001t0001g0126 a0001c0001t0001g0287 a0001c0001t0001g0288 others(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 | a0001c0002t0002g0371 a0001c0011t0001g0252 |
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 | a0001c0002t0002g0360 | 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 | a0001c0002t0002g0377 a0001c0015t0003g0374 a0002c0003t0003g0375 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0102 a0001c0001t0002g0109 others(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 | a0001c0001t0002g0217 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0109 a0001c0001t0002g0110 others(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 | a0001c0002t0002g0377 | 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 | a0001c0002t0002g0357 a0001c0002t0002g0358 a0001c0002t0002g0359 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0021 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0234 a0001c0002t0002g0057 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0366 a0001c0002t0002g0367 |
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 | a0001c0004t0001g0078 a0001c0004t0001g0079 a0001c0004t0001g0080 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0287 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0004c0006t0001g0256 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
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 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0002c0012t0002g0113 |
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 | a0001c0001t0001g0269 a0001c0001t0001g0365 a0001c0001t0001g0370 others(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 | a0001c0001t0001g0008 a0001c0001t0002g0027 a0001c0001t0002g0028 others(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 | a0001c0002t0002g0286 | 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 | a0001c0001t0001g0213 | 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 | a0002c0003t0003g0031 | 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 | a0001c0001t0002g0217 | 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 | a0001c0001t0002g0111 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0287 a0001c0001t0001g0288 others(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 | a0001c0002t0002g0125 a0001c0002t0002g0378 a0001c0002t0002g0379 others(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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0226 |
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 | a0001c0002t0002g0268 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0140 |
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 | a0001c0004t0001g0086 | 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 | a0001c0002t0002g0212 | 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 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
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 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0232 |
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 | a0007c0010t0001g0049 | 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 | a0001c0001t0005g0141 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0004t0001g0086 | 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 | a0001c0001t0001g0269 a0001c0002t0002g0270 a0001c0002t0002g0272 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0287 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 368 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(365): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0021 | 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 | a0001c0002t0002g0211 | 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 | a0001c0002t0002g0379 a0001c0002t0002g0380 |
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 | a0002c0003t0003g0030 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0365 a0001c0001t0001g0370 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0226 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0365 a0001c0001t0001g0370 others(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 | a0001c0001t0003g0101 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0287 a0001c0001t0001g0288 others(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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): 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 | a0001c0001t0001g0126 a0001c0001t0001g0287 a0001c0001t0001g0288 others(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 | a0001c0002t0002g0282 | 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 | a0001c0001t0001g0269 a0001c0001t0001g0365 a0001c0001t0001g0370 others(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 | a0004c0006t0001g0256 | 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 | a0001c0001t0004g0225 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0365 a0001c0002t0002g0250 a0001c0002t0002g0251 |
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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0002g0227 | 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 | a0002c0003t0003g0372 | 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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0033 others(40): 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0365 a0001c0001t0001g0370 a0001c0002t0002g0015 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0356 a0001c0001t0004g0230 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0378 | 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 | a0001c0011t0001g0252 | 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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0001g0021 | 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 | a0001c0002t0002g0293 a0001c0002t0002g0360 |
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 | a0001c0001t0001g0254 | 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 | a0001c0002t0002g0094 a0001c0002t0002g0095 |
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 | a0001c0002t0002g0355 | 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 | a0002c0003t0003g0369 | 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 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0013t0002g0014 |
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 | a0002c0003t0003g0051 a0002c0003t0003g0052 a0002c0003t0003g0053 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0002t0002g0349 a0001c0002t0002g0350 a0001c0002t0002g0351 others(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 | a0001c0002t0002g0294 | 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 | a0001c0001t0004g0225 | 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 | a0001c0002t0002g0371 a0001c0011t0001g0252 a0001c0015t0003g0374 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0162 | 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 | a0001c0002t0001g0348 a0001c0002t0002g0005 a0001c0002t0002g0007 others(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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0102 others(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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
111 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.95-3356C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 1/17 | chr13 | 31754902 | |||||||
| chr13:31754981 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0048 others(59): Show |
64 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(61): 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
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 | a0001c0015t0003g0374 | 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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0227 others(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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0001g0021 | 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 | a0001c0004t0001g0084 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0002t0002g0218 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
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 | a0001c0002t0002g0125 a0001c0002t0002g0378 a0001c0002t0002g0379 others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0002t0002g0251 | 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 | a0001c0002t0001g0348 | 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 | a0002c0003t0003g0285 | 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 | a0001c0001t0004g0231 | 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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
170 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(167): 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 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0341 a0001c0002t0002g0342 a0001c0002t0002g0343 |
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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0225 |
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 | a0001c0004t0001g0123 a0001c0004t0001g0124 |
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 | a0001c0002t0002g0271 | 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 | a0002c0003t0003g0087 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0370 a0001c0002t0002g0015 a0001c0002t0002g0016 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 376 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(373): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): 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 | a0001c0001t0001g0245 | 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 | a0002c0003t0003g0085 | 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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0004g0018 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0001g0151 | 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 | a0001c0015t0003g0374 | 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 | a0001c0002t0002g0371 | 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 | a0002c0003t0003g0074 | 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 | a0001c0002t0002g0057 | 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 | a0001c0002t0002g0017 a0001c0002t0002g0268 a0001c0002t0002g0271 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0021 a0001c0002t0002g0339 a0001c0002t0002g0340 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0015t0003g0374 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0226 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0032 others(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 |
34 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0114 others(31): Show |
35 | HG00099.hp2 HG00621.hp2 HG00735.hp2 others(32): 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 |
27 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(24): 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 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0004t0001g0278 |
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 | a0001c0002t0002g0337 | 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 | a0001c0001t0002g0102 | 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 | a0001c0002t0002g0015 a0001c0002t0002g0334 a0002c0003t0003g0030 others(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 | a0001c0002t0002g0377 a0001c0015t0003g0374 a0002c0003t0003g0122 others(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 | a0001c0001t0001g0356 a0001c0001t0002g0109 |
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 | a0001c0002t0002g0007 a0001c0002t0002g0323 a0001c0002t0002g0344 others(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 | a0001c0001t0001g0126 a0001c0002t0002g0361 |
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 | a0001c0001t0002g0110 a0001c0002t0002g0294 a0001c0002t0002g0373 others(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 | a0001c0001t0001g0021 a0001c0002t0002g0247 a0001c0002t0002g0309 others(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 | a0001c0001t0001g0045 a0001c0002t0002g0270 a0002c0003t0003g0077 others(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 | a0001c0001t0004g0230 a0001c0002t0002g0308 a0002c0003t0003g0024 others(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 | a0002c0003t0003g0076 a0002c0003t0003g0085 a0002c0003t0003g0104 |
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 | a0001c0001t0002g0019 a0001c0001t0004g0018 a0001c0002t0001g0348 others(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 | a0001c0002t0002g0310 a0002c0003t0003g0061 |
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 | a0001c0001t0001g0132 a0001c0002t0002g0301 a0001c0002t0002g0302 others(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 | a0001c0002t0002g0295 a0001c0002t0002g0349 a0001c0002t0002g0371 |
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 | a0001c0001t0001g0131 a0001c0002t0002g0017 a0001c0002t0002g0300 others(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 | a0002c0003t0003g0091 | 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 | a0001c0002t0002g0341 | 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 | a0001c0002t0002g0342 | 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 | a0001c0002t0002g0283 | 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 | a0001c0002t0002g0313 a0001c0002t0006g0312 a0002c0003t0003g0062 |
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 | a0001c0002t0002g0311 | 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 | a0001c0001t0002g0112 | 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 | a0001c0002t0002g0005 a0002c0003t0003g0369 |
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 | a0001c0001t0001g0105 a0001c0002t0002g0094 |
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 | a0001c0001t0001g0035 a0001c0002t0002g0351 |
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 | a0001c0001t0001g0103 a0001c0002t0002g0271 |
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 | a0003c0005t0002g0107 | 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 | a0002c0003t0003g0025 a0002c0003t0003g0046 |
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 | a0001c0001t0001g0370 a0001c0001t0004g0231 a0001c0002t0002g0293 others(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 | a0001c0002t0002g0249 a0001c0002t0002g0296 a0001c0002t0002g0316 others(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 | a0001c0001t0002g0020 a0001c0002t0002g0314 a0001c0002t0002g0315 others(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 | a0002c0003t0003g0052 | 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 | a0001c0002t0002g0325 | 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 | a0001c0002t0002g0108 a0001c0002t0002g0298 a0001c0002t0002g0322 others(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 | a0001c0001t0001g0133 a0001c0002t0002g0218 a0001c0002t0002g0320 others(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 | a0001c0001t0002g0111 a0001c0002t0002g0095 a0001c0002t0002g0286 others(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 | a0001c0002t0002g0352 a0001c0002t0002g0366 a0002c0003t0003g0075 |
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 | a0001c0002t0002g0381 | 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 | a0002c0003t0003g0375 | 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 | a0001c0002t0002g0324 | 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 | a0001c0002t0002g0355 | 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 | a0001c0002t0002g0359 | 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 | a0001c0001t0004g0232 a0001c0002t0002g0268 a0001c0002t0002g0329 others(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 | a0001c0001t0001g0042 a0001c0002t0002g0043 a0001c0013t0002g0014 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0233 a0001c0002t0002g0284 others(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 | a0001c0001t0002g0227 a0001c0002t0002g0326 a0001c0002t0002g0340 others(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 | a0002c0003t0003g0221 | 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 | a0001c0002t0002g0335 | 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 | a0001c0001t0001g0130 a0001c0002t0002g0219 |
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 | a0001c0002t0002g0016 | 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 | a0001c0002t0002g0333 a0002c0003t0003g0072 |
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 | a0001c0001t0001g0044 a0001c0002t0002g0332 a0002c0003t0003g0071 |
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 | a0001c0002t0002g0216 a0001c0002t0006g0336 |
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 | a0001c0002t0002g0364 a0002c0003t0003g0106 |
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 | a0001c0002t0002g0235 a0002c0003t0003g0073 |
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 | a0002c0003t0003g0376 | 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 | a0001c0001t0004g0225 | 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 | a0001c0001t0001g0264 | 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 | a0001c0002t0002g0338 | 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 | a0001c0001t0003g0101 | 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 | a0001c0001t0008g0204 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0200 a0001c0001t0001g0208 |
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 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0222 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0134 a0001c0002t0002g0363 |
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 | a0001c0001t0002g0006 a0001c0002t0002g0135 a0001c0002t0002g0282 others(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 | a0001c0002t0002g0211 | 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 | a0001c0002t0002g0272 a0002c0003t0003g0092 a0003c0005t0002g0229 |
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 | a0001c0002t0002g0331 | 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 | a0001c0002t0002g0253 | 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 | a0002c0003t0003g0067 | 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 | a0002c0003t0003g0063 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0047 | 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 | a0001c0002t0002g0362 | 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 | a0001c0002t0002g0321 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0105 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0002t0002g0007 | 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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0002t0002g0337 | 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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0109 a0001c0001t0002g0110 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0002c0003t0003g0063 a0002c0003t0003g0067 |
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 | a0001c0001t0001g0234 | 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 | a0002c0003t0003g0056 a0002c0003t0003g0058 a0002c0003t0003g0062 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0109 a0001c0001t0002g0110 others(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 | a0001c0002t0002g0282 a0001c0002t0002g0283 a0001c0002t0002g0284 |
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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0009 | 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 | a0001c0002t0002g0357 | 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 | a0001c0002t0002g0007 | 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 | a0002c0003t0003g0052 a0002c0003t0003g0053 a0002c0003t0003g0054 |
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 | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
116 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(113): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0370 | 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 | a0001c0001t0001g0126 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0002t0002g0125 a0001c0002t0002g0371 a0001c0002t0002g0378 others(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 | a0001c0002t0002g0320 a0001c0002t0002g0338 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0261 | 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 | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0002t0002g0377 others(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 | a0001c0001t0002g0020 | 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 | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): 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 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0126 a0001c0001t0002g0020 a0001c0015t0003g0374 |
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 | 74 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0038 others(71): 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 | a0001c0001t0001g0008 a0001c0001t0001g0152 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0037 others(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 |
3 | a0001c0001t0001g0003 a0001c0001t0001g0258 a0002c0012t0002g0113 |
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 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 others(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 |
4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | NA18968.hp2 NA18982.hp2 NA19004.hp2 others(1): 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0110 a0001c0001t0002g0111 |
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 | a0001c0001t0001g0133 a0001c0001t0001g0171 a0001c0001t0001g0254 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0088 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0224 a0001c0004t0001g0116 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0021 | 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 | a0001c0002t0002g0135 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0105 a0002c0003t0003g0085 a0008c0007t0003g0064 |
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 | a0001c0002t0002g0377 a0002c0003t0003g0050 a0002c0003t0003g0070 others(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 | a0002c0003t0003g0024 a0002c0003t0003g0030 a0002c0003t0003g0031 others(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 | a0002c0003t0003g0023 a0002c0003t0003g0025 a0002c0003t0003g0026 others(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 | a0002c0003t0003g0071 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0002t0002g0377 others(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 | a0001c0002t0001g0348 a0001c0002t0002g0005 a0001c0002t0002g0007 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0044 |
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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0002t0002g0377 others(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 | a0001c0002t0002g0275 a0001c0002t0002g0276 a0001c0002t0002g0277 |
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 | a0001c0002t0002g0381 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0105 others(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 | a0001c0001t0002g0161 | 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 | a0001c0001t0001g0246 | 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 | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0033 others(47): 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
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 | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): 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 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0001g0224 others(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 | a0001c0002t0002g0125 a0001c0002t0002g0378 a0001c0002t0002g0379 others(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 | a0001c0002t0002g0125 a0001c0002t0002g0378 a0001c0002t0002g0379 others(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 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0132 | 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 | a0001c0002t0002g0293 a0001c0002t0002g0316 a0001c0002t0002g0360 |
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 | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(327): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0356 | 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 | a0001c0001t0001g0160 a0001c0001t0002g0159 a0001c0001t0002g0161 |
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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0002t0002g0377 others(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 | a0002c0003t0003g0031 a0002c0003t0003g0046 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0109 a0001c0001t0002g0110 others(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 | a0001c0001t0001g0114 | 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 | a0001c0002t0002g0212 | 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 | a0003c0005t0002g0107 | 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 | a0001c0002t0002g0317 a0001c0002t0007g0327 |
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 | a0001c0002t0002g0322 | 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 | a0002c0003t0003g0030 a0002c0003t0003g0091 a0002c0003t0003g0092 others(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 | a0001c0001t0001g0011 | 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 | a0001c0002t0002g0371 a0001c0011t0001g0252 |
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 | a0001c0001t0001g0088 | 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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0002t0002g0329 | 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 | 2 | a0001c0001t0001g0004 a0001c0001t0001g0265 |
3 | HG00280.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.497+2276C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 5/17 | chr13 | 31768303 | |||||||
| chr13:31768474 | G | A | 14 | a0001c0002t0002g0009 a0001c0002t0002g0015 a0001c0002t0002g0016 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0226 |
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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0002c0003t0003g0052 a0002c0003t0003g0053 a0002c0003t0003g0054 others(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 | a0001c0002t0002g0125 a0001c0002t0002g0378 a0001c0002t0002g0379 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0088 a0001c0001t0001g0089 others(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 | a0001c0002t0002g0146 | 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 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
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 | a0001c0001t0001g0167 | 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 | 22 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0148 others(19): 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 | a0001c0002t0002g0125 a0001c0002t0002g0378 a0001c0002t0002g0379 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0224 a0001c0001t0002g0006 others(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 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(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 | a0007c0010t0001g0049 | 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 | a0001c0001t0001g0126 a0001c0002t0001g0348 a0001c0002t0002g0005 others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0013t0002g0014 others(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 | a0001c0001t0001g0201 | 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 | a0001c0002t0002g0379 a0001c0002t0002g0380 |
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 | a0001c0001t0001g0166 a0001c0015t0003g0374 |
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 | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
262 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(259): 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 | a0001c0001t0001g0090 a0001c0001t0001g0134 a0001c0001t0001g0213 others(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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): 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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0013t0002g0014 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0356 others(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 | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
262 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(259): 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0013t0002g0014 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0224 |
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 | a0001c0002t0002g0275 a0001c0002t0002g0276 a0001c0002t0002g0277 |
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 | a0002c0003t0003g0030 a0002c0003t0003g0091 a0002c0003t0003g0092 others(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 | a0001c0002t0002g0371 a0001c0011t0001g0252 |
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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0190 a0001c0001t0008g0204 |
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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
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 | a0002c0003t0003g0076 a0002c0003t0003g0077 |
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 | a0001c0002t0002g0145 | 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 | a0002c0003t0003g0375 a0002c0003t0003g0376 |
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 | a0001c0002t0002g0371 | 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 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0257 others(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 | a0001c0002t0002g0371 | 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 | a0002c0003t0003g0087 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0224 a0001c0001t0002g0006 others(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 | a0001c0002t0002g0125 a0001c0002t0002g0378 a0001c0002t0002g0379 others(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 | a0001c0002t0002g0371 a0001c0011t0001g0252 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0126 a0001c0001t0003g0100 a0001c0001t0003g0101 others(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 | a0002c0003t0003g0075 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0145 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0013t0002g0014 others(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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
124 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(121): 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 | a0001c0001t0001g0166 | 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 | a0001c0004t0001g0078 | 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 | a0001c0002t0002g0043 a0001c0002t0002g0155 a0001c0002t0002g0251 |
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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0002t0002g0135 | 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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0015t0003g0374 | 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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(77): Show |
81 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(78): 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 | a0001c0001t0001g0224 a0001c0001t0002g0102 a0001c0001t0002g0110 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0226 |
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 | a0002c0012t0002g0113 | 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 | 31 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0033 others(28): 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 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0036 others(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 | a0001c0001t0002g0227 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0032 others(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 | a0001c0001t0004g0232 a0001c0002t0002g0125 a0001c0002t0002g0371 others(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 | a0001c0001t0002g0227 a0001c0001t0004g0230 a0001c0001t0004g0231 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0032 others(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 | a0001c0001t0002g0227 a0001c0001t0004g0230 a0001c0001t0004g0231 others(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 | a0001c0002t0002g0125 a0001c0002t0002g0371 a0003c0005t0002g0228 |
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 | a0001c0001t0001g0356 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0002g0379 a0001c0002t0002g0380 |
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 | 49 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0156 others(46): 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 | 40 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0034 others(37): Show |
41 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(38): 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 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 |
39 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0042 others(36): 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 | a0001c0001t0001g0045 a0001c0001t0001g0160 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0137 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0193 | 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 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0095 others(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 | a0001c0002t0001g0348 a0001c0002t0002g0009 a0001c0002t0002g0108 others(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 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0043 others(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 | a0001c0002t0002g0216 a0001c0002t0002g0311 a0001c0002t0002g0337 others(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 | a0001c0002t0002g0057 a0001c0002t0002g0250 a0001c0002t0002g0275 |
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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0276 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0021 | 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 | a0001c0002t0002g0378 a0003c0005t0002g0107 a0003c0005t0002g0229 |
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 | a0001c0002t0002g0378 a0003c0005t0002g0107 a0003c0005t0002g0229 |
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 | a0001c0001t0001g0021 | 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 | a0001c0001t0002g0227 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
138 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.641+799T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 7/17 | chr13 | 31776188 | |||||||
| chr13:31776253 | C | CT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
130 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0129 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0003g0100 others(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 | a0001c0002t0002g0371 a0001c0011t0001g0252 |
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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0013t0002g0014 others(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 | 12 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0234 others(9): 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 | a0001c0002t0002g0313 | 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 | a0001c0002t0002g0125 a0001c0002t0002g0378 a0001c0002t0002g0379 others(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 | a0001c0002t0002g0043 a0001c0002t0002g0155 a0001c0002t0002g0251 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0145 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0224 |
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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0002t0002g0371 a0001c0011t0001g0252 |
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 | a0002c0003t0003g0031 a0002c0003t0003g0046 |
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 | a0001c0001t0005g0183 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0002t0002g0305 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0224 |
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 | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
223 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.785+380C>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31778963 | |||||||
| chr13:31779122 | T | TTA | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): 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 | a0001c0001t0001g0035 a0001c0001t0001g0168 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0243 a0001c0001t0002g0019 a0001c0001t0002g0102 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0168 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0168 a0001c0001t0001g0169 others(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 | a0001c0002t0002g0043 a0001c0002t0002g0155 a0001c0002t0002g0251 |
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 | a0001c0001t0002g0102 a0001c0001t0002g0112 |
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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0013t0002g0014 others(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 | a0001c0002t0002g0218 | 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 | 2 | a0001c0001t0001g0004 a0001c0001t0001g0265 |
3 | HG00280.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.785+1015C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 9/17 | chr13 | 31779598 | |||||||
| chr13:31779654 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
263 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(260): 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 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0266 others(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 | a0001c0001t0002g0159 a0001c0001t0002g0161 |
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 | a0001c0002t0002g0378 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0356 a0001c0004t0001g0022 a0001c0004t0001g0078 others(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 | a0001c0002t0002g0286 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
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 | a0001c0002t0002g0328 | 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 | a0002c0003t0003g0085 | 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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
140 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(137): 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 | a0009c0014t0002g0303 | 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 | a0001c0001t0001g0012 a0001c0001t0002g0019 a0001c0001t0002g0020 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0250 | 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 | a0001c0001t0001g0182 | 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): 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 | a0001c0002t0002g0373 | 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 | a0001c0001t0001g0274 | 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 | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(362): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0152 | 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 | a0001c0002t0002g0270 | 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): 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 | a0002c0003t0003g0031 a0002c0003t0003g0046 |
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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0002t0002g0305 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
219 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(216): 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0152 | 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 | a0006c0009t0001g0163 | 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 | a0001c0004t0001g0022 a0001c0004t0001g0078 a0001c0004t0001g0079 others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0002g0217 | 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 | a0002c0003t0003g0055 | 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): 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 | a0001c0001t0001g0201 | 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.929+459C>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783206 | |||||||
| chr13:31783221 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.929+474A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31783221 | |||||||
| chr13:31783398 | T | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): 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 | a0001c0001t0002g0020 | 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 | a0001c0004t0001g0127 | 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): 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 | a0001c0015t0003g0374 | 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 | a0001c0015t0003g0374 | 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 | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): 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 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): 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 | a0001c0002t0002g0322 | 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 | a0001c0002t0002g0043 a0001c0002t0002g0057 a0001c0002t0002g0135 others(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 | a0001c0001t0001g0356 a0001c0002t0001g0348 a0001c0002t0002g0005 others(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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0002t0002g0094 others(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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0227 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0028 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0144 others(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 |
118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): 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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0269 a0001c0001t0001g0287 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0160 | 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 | a0001c0015t0003g0374 | 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.929+1343A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31784090 | |||||||
| chr13:31784123 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): 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 | a0001c0011t0001g0252 | 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 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0002t0002g0268 | 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 | a0001c0001t0001g0048 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0217 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.930-1116C>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785267 | |||||||
| chr13:31785319 | G | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): 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 | a0001c0002t0002g0361 a0001c0002t0002g0362 a0001c0002t0002g0363 others(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 | a0001c0002t0002g0305 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
142 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.930-742A>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785641 | |||||||
| chr13:31785749 | A | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
142 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.930-634A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31785749 | |||||||
| chr13:31785823 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): 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 | a0001c0002t0002g0286 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0037 others(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 | a0001c0015t0003g0374 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.930-241T>G | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 11/17 | chr13 | 31786142 | |||||||
| chr13:31786212 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0002t0002g0344 a0001c0002t0002g0345 a0001c0002t0002g0346 others(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 | a0001c0002t0002g0299 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0260 | 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 | a0001c0013t0002g0014 a0002c0003t0003g0023 a0002c0003t0003g0024 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(98): 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 | 103 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0001t0001g0178 | 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 | a0001c0002t0002g0145 | 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 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0232 |
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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0001t0001g0193 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0001t0001g0164 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0356 | 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 | a0004c0006t0001g0256 | 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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0002c0003t0003g0073 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0002t0006g0312 | 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 | a0001c0002t0002g0009 a0001c0002t0002g0015 a0001c0002t0002g0016 others(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 | a0001c0002t0001g0348 a0001c0002t0002g0005 a0001c0002t0002g0007 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0209 a0001c0001t0002g0217 others(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 | a0001c0001t0001g0233 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): 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 | a0001c0002t0002g0307 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0037 others(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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0002t0002g0315 | 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 | a0001c0015t0003g0374 | 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 | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): 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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0152 others(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 | a0001c0001t0004g0232 | 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 | a0001c0013t0002g0014 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0232 |
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 | a0001c0001t0002g0159 a0001c0001t0002g0161 |
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 | a0001c0002t0002g0043 a0001c0002t0002g0155 a0001c0002t0002g0251 others(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 | a0001c0001t0001g0265 | 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 | a0001c0002t0001g0348 a0001c0002t0002g0005 a0001c0002t0002g0007 others(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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0003g0100 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0214 | 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 | a0001c0013t0002g0014 | 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 | a0001c0002t0001g0348 a0001c0002t0002g0304 a0001c0002t0002g0325 |
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 | a0001c0001t0002g0112 | 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 | a0001c0002t0001g0348 a0001c0002t0002g0005 a0001c0002t0002g0007 others(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 | a0001c0001t0002g0006 | 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 | a0001c0002t0002g0302 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 |
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 | a0001c0001t0001g0259 | 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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0003g0100 others(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 | a0001c0002t0002g0355 | 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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0003g0100 others(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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0003g0100 others(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 | a0001c0002t0002g0235 | 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 | a0001c0001t0004g0230 | 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 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
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 | a0001c0001t0001g0224 a0001c0001t0002g0006 a0001c0001t0002g0027 others(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 | a0001c0001t0005g0192 a0001c0002t0002g0015 a0001c0002t0002g0016 others(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 | a0001c0001t0001g0045 | 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 | a0001c0002t0002g0379 a0001c0002t0002g0380 |
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 | a0001c0001t0001g0160 | 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 | a0001c0002t0001g0348 a0001c0002t0002g0005 a0001c0002t0002g0007 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0144 others(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 | a0001c0001t0004g0225 a0001c0002t0002g0015 a0001c0002t0002g0016 others(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 | a0001c0001t0004g0018 a0001c0002t0002g0009 a0001c0002t0002g0247 others(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 | a0001c0002t0002g0125 a0001c0002t0002g0249 a0001c0002t0002g0268 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0001t0002g0102 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): 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 | a0001c0001t0001g0003 a0001c0001t0001g0186 a0001c0002t0002g0108 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0150 others(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 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0232 |
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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0003g0100 others(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 | a0001c0001t0004g0018 a0001c0001t0004g0225 a0001c0002t0002g0043 others(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 | a0001c0011t0001g0252 | 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 | a0002c0003t0003g0030 a0002c0003t0003g0091 a0002c0003t0003g0092 |
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 | a0002c0003t0003g0106 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0037 others(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 | a0002c0003t0003g0068 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0002t0002g0270 a0001c0002t0002g0272 |
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 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0037 others(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 | a0001c0002t0002g0381 | 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 | a0001c0001t0001g0140 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1787-1574G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 16/17 | chr13 | 31795627 | |||||||
| chr13:31795800 | G | A | 1 | a0001c0015t0003g0374 | 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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): 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 | a0001c0001t0001g0150 a0001c0001t0001g0172 a0001c0001t0001g0191 others(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 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0232 |
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 | a0001c0002t0001g0348 a0001c0002t0002g0005 a0001c0002t0002g0007 others(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 | a0003c0005t0002g0229 | 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 | a0001c0002t0002g0297 a0001c0002t0002g0300 |
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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0002t0002g0271 | 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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0224 |
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 | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): 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 | a0001c0001t0001g0004 a0001c0001t0001g0265 |
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 | a0002c0003t0003g0031 a0002c0003t0003g0046 |
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 | a0001c0001t0001g0224 | 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 | a0001c0002t0002g0155 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0224 a0001c0001t0003g0100 others(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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): 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 | a0001c0001t0001g0021 a0001c0001t0001g0224 a0001c0001t0003g0100 others(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 | a0001c0001t0005g0183 | 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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0253 | 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 | a0001c0001t0001g0202 | 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0206 others(10): 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 | a0001c0001t0002g0102 a0001c0001t0002g0112 a0001c0001t0004g0018 others(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 | a0001c0002t0002g0043 a0001c0002t0002g0155 a0001c0002t0002g0251 |
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 | a0001c0002t0002g0323 | 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 | a0001c0002t0002g0235 | 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 | a0001c0011t0001g0252 | 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 | 362 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(359): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0005g0141 | 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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
140 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(137): 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 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0002t0002g0275 others(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 | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
137 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(134): 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 | a0001c0002t0002g0323 | 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 | a0001c0001t0002g0227 | 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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0015t0003g0374 |
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 | a0002c0003t0003g0050 a0002c0003t0003g0070 |
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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
138 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(135): 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 | a0001c0011t0001g0252 | 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 | a0001c0002t0002g0043 a0001c0002t0002g0155 a0001c0002t0002g0251 |
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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
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 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0094 others(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 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0015t0003g0374 others(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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0198 | 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 | a0001c0004t0001g0118 | 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 | a0003c0005t0002g0107 a0003c0005t0002g0228 a0003c0005t0002g0229 |
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 | a0001c0001t0002g0006 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0004t0001g0127 | 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 | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2006-1588T>C | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800558 | |||||||
| chr13:31800651 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2006-1495G>A | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800651 | |||||||
| chr13:31800839 | A | ATT | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): 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 | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2006-1299A>T | RXFP2 | ENSG00000133105.8 | transcript | ENST00000298386.7 | protein_coding | 17/17 | chr13 | 31800847 | |||||||
| chr13:31801017 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
150 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(147): 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 | a0001c0004t0001g0078 | 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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
140 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(137): 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0002g0043 a0001c0002t0002g0251 |
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 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0015t0003g0374 |
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 | a0001c0001t0001g0042 | 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 | a0001c0002t0002g0299 | 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 | a0001c0001t0001g0042 | 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 | a0001c0002t0002g0323 | 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 | a0001c0002t0002g0323 | 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 | a0002c0003t0003g0051 a0002c0003t0003g0052 a0002c0003t0003g0053 others(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 | a0001c0001t0001g0261 | 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
138 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(135): 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 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0232 |
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 |