Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 653519 |
| ensemblid | ENSG00000117262.19 |
| hgncid | 31984 |
| symbol | GPR89A |
| name | G protein-coupled receptor 89A |
| refseq_nuc | NM_001097612.2 |
| refseq_prot | NP_001091081.1 |
| ensembl_nuc | ENST00000313835.14 |
| ensembl_prot | ENSP00000319673.9 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 145607988 |
| end | 145670650 |
| strand | + |
| ver | v1.2 |
| region | chr1:145607988-145670650 |
| region5000 | chr1:145602988-145675650 |
| regionname0 | GPR89A_chr1_145607988_145670650 |
| regionname5000 | GPR89A_chr1_145602988_145675650 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 455 | 273 | 74 | 46 | 111 | 10 | 30 | 82 | GPR89A_chr1_145602988_145675650 | GPR89A | MSFLI others(450): Show |
chr1 | 145602988 | 145675650 |
| a0002 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | MSFLI others(450): Show |
chr1 | 145602988 | 145675650 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1365 | 253 | 57 | 46 | 108 | 10 | 30 | GPR89A_chr1_145602988_145675650 | GPR89A | ATGAG others(1360): Show |
chr1 | 145602988 | 145675650 | ||
| a0001c0002 | 0/0 | 1365 | 16 | 16 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | ATGAG others(1360): Show |
chr1 | 145602988 | 145675650 | ||
| a0001c0003 | 0/0 | 1365 | 3 | 0 | 0 | 3 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | ATGAG others(1360): Show |
chr1 | 145602988 | 145675650 | ||
| a0001c0004 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | ATGAG others(1360): Show |
chr1 | 145602988 | 145675650 | ||
| a0002c0005 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | ATGAG others(1360): Show |
chr1 | 145602988 | 145675650 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2124 | 248 | 54 | 46 | 106 | 10 | 30 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0001c0001t0003 | 0/0 | 2124 | 3 | 3 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0001c0001t0004 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0001c0001t0006 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0001c0002t0001 | 0/0 | 2124 | 11 | 11 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0001c0002t0002 | 0/0 | 2124 | 4 | 4 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0001c0002t0005 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0001c0003t0001 | 0/0 | 2124 | 3 | 0 | 0 | 3 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0001c0004t0001 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| a0002c0005t0001 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | GCAGC others(2119): Show |
chr1 | 145602988 | 145675650 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 1 | 1 | 2 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0004 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0001c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| a0002c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00609 | hp1 | a0002 | c0005 | t0001 | g0242 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0082 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0136 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0134 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | YRI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18985 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0028 | AFR | LWK | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | YRI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ASW | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ASW | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | USA | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0097 | REF | REF | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0206 | REF | REF | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:145646192 | C | G | 1 | a0002 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.736C>G | p.Leu246Val | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 9/14 | 882/2124 | 736/1368 | 246/455 | chr1 | 145646192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:145608145 | C | G | 1 | a0001c0002 | 16 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(13): Show |
synonymous_variant | LOW | c.12C>G | p.Leu4Leu | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/14 | 158/2124 | 12/1368 | 4/455 | chr1 | 145608145 | |||
| chr1:145616293 | G | A | 1 | a0001c0003 | 3 | NA18985.hp1 NA19058.hp1 NA19079.hp1 |
splice_region_variant&synonymous_variant | LOW | c.102G>A | p.Glu34Glu | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/14 | 248/2124 | 102/1368 | 34/455 | chr1 | 145616293 | |||
| chr1:145623635 | T | C | 1 | a0001c0004 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.336T>C | p.Phe112Phe | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/14 | 482/2124 | 336/1368 | 112/455 | chr1 | 145623635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:145608091 | G | C | 1 | a0001c0002t0002 | 4 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-43G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/14 | 43 | chr1 | 145608091 | ||||||
| chr1:145670191 | G | A | 1 | a0001c0001t0004 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 14/14 | 151 | chr1 | 145670191 | ||||||
| chr1:145670207 | T | C | 1 | a0001c0002t0005 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*167T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 14/14 | 167 | chr1 | 145670207 | ||||||
| chr1:145670274 | G | A | 1 | a0001c0001t0006 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 14/14 | 234 | chr1 | 145670274 | ||||||
| chr1:145670393 | G | A | 1 | a0001c0001t0003 | 3 | HG02257.hp1 HG02559.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*353G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 14/14 | 353 | chr1 | 145670393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:145608181 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | splice_region_variant&intron_variant | LOW | c.42+6T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608181 | |||||||
| chr1:145608219 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42+44A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608219 | |||||||
| chr1:145608243 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.42+68C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608243 | |||||||
| chr1:145608272 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.42+97C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608272 | |||||||
| chr1:145608293 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.42+118T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608293 | |||||||
| chr1:145608386 | C | T | 5 | a0001c0002t0001g0138 a0001c0002t0002g0134 a0001c0002t0002g0135 others(2): Show |
5 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+211C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608386 | |||||||
| chr1:145608435 | C | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.42+260C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608435 | |||||||
| chr1:145608582 | A | G | 5 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(2): Show |
5 | HG00609.hp1 HG02040.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+407A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608582 | |||||||
| chr1:145608969 | G | A | 5 | a0001c0002t0001g0138 a0001c0002t0002g0134 a0001c0002t0002g0135 others(2): Show |
5 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+794G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608969 | |||||||
| chr1:145608972 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.42+797C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145608972 | |||||||
| chr1:145609108 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.42+933G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609108 | |||||||
| chr1:145609121 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.42+946C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609121 | |||||||
| chr1:145609122 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.42+947C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609122 | |||||||
| chr1:145609129 | C | G | 19 | a0001c0001t0001g0006 a0001c0001t0001g0221 a0001c0001t0001g0222 others(16): Show |
20 | HG00438.hp1 HG02074.hp1 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.42+954C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609129 | |||||||
| chr1:145609183 | G | A | 5 | a0001c0002t0001g0138 a0001c0002t0002g0134 a0001c0002t0002g0135 others(2): Show |
5 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1008G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609183 | |||||||
| chr1:145609212 | G | C | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+1037G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609212 | |||||||
| chr1:145609260 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.42+1085C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609260 | |||||||
| chr1:145609705 | G | A | 5 | a0001c0002t0001g0138 a0001c0002t0002g0134 a0001c0002t0002g0135 others(2): Show |
5 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1530G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609705 | |||||||
| chr1:145609830 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.42+1655C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609830 | |||||||
| chr1:145609918 | C | T | 5 | a0001c0002t0001g0138 a0001c0002t0002g0134 a0001c0002t0002g0135 others(2): Show |
5 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1743C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609918 | |||||||
| chr1:145609976 | C | T | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.42+1801C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145609976 | |||||||
| chr1:145610050 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0118 others(12): Show |
17 | HG01175.hp2 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.42+1875C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610050 | |||||||
| chr1:145610179 | T | C | 4 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+2004T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610179 | |||||||
| chr1:145610292 | C | G | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG00735.hp1 HG01099.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2117C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610292 | |||||||
| chr1:145610374 | C | T | 3 | a0001c0003t0001g0111 a0001c0003t0001g0112 a0001c0003t0001g0113 |
3 | NA18985.hp1 NA19058.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.42+2199C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610374 | |||||||
| chr1:145610439 | C | T | 5 | a0001c0002t0001g0138 a0001c0002t0002g0134 a0001c0002t0002g0135 others(2): Show |
5 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+2264C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610439 | |||||||
| chr1:145610445 | G | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.42+2270G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610445 | |||||||
| chr1:145610451 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.42+2276A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610451 | |||||||
| chr1:145610532 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.42+2357G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610532 | |||||||
| chr1:145610620 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.42+2445C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610620 | |||||||
| chr1:145610645 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0108 a0001c0001t0001g0109 |
4 | HG03041.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2470G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610645 | |||||||
| chr1:145610866 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+2691C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145610866 | |||||||
| chr1:145611160 | T | TTG | 12 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0098 others(9): Show |
16 | HG00423.hp2 HG01168.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.42+3005_42+3006dup others(2): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 145611160 | ||||||
| chr1:145611160 | TTG | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+3005_42+3006del others(2): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 145611160 | ||||||
| chr1:145611191 | C | CT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
140 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.42+3029dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 145611191 | ||||||
| chr1:145611240 | C | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+3065C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145611240 | |||||||
| chr1:145611463 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+3288A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145611463 | |||||||
| chr1:145611762 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+3587G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145611762 | |||||||
| chr1:145611794 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.42+3619A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145611794 | |||||||
| chr1:145611961 | A | G | 2 | a0001c0003t0001g0112 a0001c0003t0001g0113 |
2 | NA18985.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.42+3786A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145611961 | |||||||
| chr1:145611971 | A | G | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+3796A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145611971 | |||||||
| chr1:145612173 | T | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+3998T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145612173 | |||||||
| chr1:145612401 | G | A | 5 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(2): Show |
5 | HG02922.hp2 HG03195.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-3833G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145612401 | |||||||
| chr1:145612473 | A | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-3761A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145612473 | |||||||
| chr1:145612474 | A | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-3760A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145612474 | |||||||
| chr1:145612665 | G | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG00621.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.43-3569G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145612665 | |||||||
| chr1:145612866 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.43-3368A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145612866 | |||||||
| chr1:145612943 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.43-3291A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145612943 | |||||||
| chr1:145613016 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.43-3218T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613016 | |||||||
| chr1:145613125 | T | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-3109T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613125 | |||||||
| chr1:145613396 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-2838A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613396 | |||||||
| chr1:145613458 | A | G | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2776A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613458 | |||||||
| chr1:145613484 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG02258.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.43-2750A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613484 | |||||||
| chr1:145613611 | C | T | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-2623C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613611 | |||||||
| chr1:145613691 | T | C | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.43-2543T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613691 | |||||||
| chr1:145613833 | C | G | 1 | a0002c0005t0001g0242 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.43-2401C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613833 | |||||||
| chr1:145613868 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.43-2366C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145613868 | |||||||
| chr1:145614164 | C | G | 4 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2070C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145614164 | |||||||
| chr1:145614339 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.43-1895C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145614339 | |||||||
| chr1:145614440 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.43-1794C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145614440 | |||||||
| chr1:145615176 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-1058G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145615176 | |||||||
| chr1:145615288 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43-946C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145615288 | |||||||
| chr1:145615292 | T | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-942T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145615292 | |||||||
| chr1:145615441 | T | G | 1 | a0001c0001t0001g0034 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.43-793T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145615441 | |||||||
| chr1:145615487 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.43-747G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145615487 | |||||||
| chr1:145615662 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.43-572A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145615662 | |||||||
| chr1:145615958 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.43-276A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145615958 | |||||||
| chr1:145616089 | A | AG | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-145_43-144insG | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145616089 | |||||||
| chr1:145616119 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.43-115A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145616119 | |||||||
| chr1:145616218 | T | C | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.43-16T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145616218 | |||||||
| chr1:145616330 | G | GA | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.102+38dupA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 145616330 | ||||||
| chr1:145616654 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.102+361C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145616654 | |||||||
| chr1:145616670 | T | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0092 |
3 | HG02027.hp1 HG02135.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.102+377T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145616670 | |||||||
| chr1:145616686 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102+393C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145616686 | |||||||
| chr1:145616697 | A | G | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.102+404A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145616697 | |||||||
| chr1:145616731 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.102+438C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145616731 | |||||||
| chr1:145617193 | A | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.102+900A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145617193 | |||||||
| chr1:145617273 | A | C | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.102+980A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145617273 | |||||||
| chr1:145617404 | T | G | 14 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0002t0001g0023 others(11): Show |
14 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.103-916T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145617404 | |||||||
| chr1:145617505 | T | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.103-815T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145617505 | |||||||
| chr1:145617544 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.103-776A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145617544 | |||||||
| chr1:145618242 | A | C | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.103-78A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145618242 | |||||||
| chr1:145618295 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.103-25C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145618295 | |||||||
| chr1:145618633 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.206+210C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145618633 | |||||||
| chr1:145618673 | T | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+250T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145618673 | |||||||
| chr1:145618983 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+560T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145618983 | |||||||
| chr1:145619107 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+684C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619107 | |||||||
| chr1:145619117 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG02300.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.206+694G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619117 | |||||||
| chr1:145619170 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0216 |
2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.206+747A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619170 | |||||||
| chr1:145619303 | T | TAA | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.206+892_206+893dup others(2): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 145619303 | ||||||
| chr1:145619317 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.206+894G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619317 | |||||||
| chr1:145619318 | A | AAG | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.206+902_206+903dup others(2): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 145619318 | ||||||
| chr1:145619318 | A | AG | 14 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(11): Show |
14 | HG01167.hp1 HG01261.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.206+895_206+896ins others(1): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619318 | |||||||
| chr1:145619318 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.206+895A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619318 | |||||||
| chr1:145619413 | G | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+990G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619413 | |||||||
| chr1:145619464 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+1041T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619464 | |||||||
| chr1:145619555 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0237 |
2 | HG02129.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.206+1132A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619555 | |||||||
| chr1:145619644 | C | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+1221C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619644 | |||||||
| chr1:145619742 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+1319A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619742 | |||||||
| chr1:145619787 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+1364A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619787 | |||||||
| chr1:145619876 | G | A | 2 | a0001c0001t0001g0237 a0001c0002t0001g0138 |
2 | HG02129.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.206+1453G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619876 | |||||||
| chr1:145620022 | TAAATAAA others(4): Show |
T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+1606_206+1616d others(13): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 145620022 | ||||||
| chr1:145620127 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.206+1704T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620127 | |||||||
| chr1:145620132 | A | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0216 |
2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.206+1709A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620132 | |||||||
| chr1:145620177 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.206+1754G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620177 | |||||||
| chr1:145620194 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+1771G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620194 | |||||||
| chr1:145620202 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+1779A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620202 | |||||||
| chr1:145620270 | A | C | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+1847A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620270 | |||||||
| chr1:145620275 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+1852A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620275 | |||||||
| chr1:145620339 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+1916G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620339 | |||||||
| chr1:145620513 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.206+2090C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620513 | |||||||
| chr1:145620577 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.206+2154G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620577 | |||||||
| chr1:145620807 | G | C | 1 | a0001c0001t0001g0037 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.207-2247G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145620807 | |||||||
| chr1:145621235 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.207-1819A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145621235 | |||||||
| chr1:145621272 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.207-1782A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145621272 | |||||||
| chr1:145621520 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.207-1534T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145621520 | |||||||
| chr1:145622353 | G | A | 1 | a0001c0001t0001g0007 | 2 | NA19003.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.207-701G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145622353 | |||||||
| chr1:145622491 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.207-563C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145622491 | |||||||
| chr1:145622658 | G | T | 2 | a0001c0002t0001g0026 a0001c0002t0001g0027 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.207-396G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145622658 | |||||||
| chr1:145623005 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.207-49G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145623005 | |||||||
| chr1:145623272 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.313+112A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 4/13 | chr1 | 145623272 | |||||||
| chr1:145623452 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.314-161C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 4/13 | chr1 | 145623452 | |||||||
| chr1:145624083 | A | T | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.415+369A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624083 | |||||||
| chr1:145624293 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.415+579C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624293 | |||||||
| chr1:145624362 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.415+648A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624362 | |||||||
| chr1:145624414 | TGAATCTA others(15): Show |
T | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.415+725_415+746del others(22): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 145624414 | ||||||
| chr1:145624425 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+711A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624425 | |||||||
| chr1:145624511 | A | AAT | 9 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(6): Show |
9 | HG02055.hp1 HG02630.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+798_415+799ins others(2): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 145624511 | ||||||
| chr1:145624513 | A | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+799A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624513 | |||||||
| chr1:145624516 | C | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+802C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624516 | |||||||
| chr1:145624591 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.415+877A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624591 | |||||||
| chr1:145624854 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.415+1140C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624854 | |||||||
| chr1:145624869 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.415+1155T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624869 | |||||||
| chr1:145624934 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.415+1220C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145624934 | |||||||
| chr1:145625092 | ACT | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0143 others(29): Show |
33 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.415+1382_415+1383d others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 145625092 | ||||||
| chr1:145625159 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.415+1445G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625159 | |||||||
| chr1:145625211 | C | T | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.415+1497C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625211 | |||||||
| chr1:145625265 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
12 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+1551G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625265 | |||||||
| chr1:145625500 | C | T | 1 | a0001c0004t0001g0082 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.415+1786C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625500 | |||||||
| chr1:145625506 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.415+1792A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625506 | |||||||
| chr1:145625583 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+1869A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625583 | |||||||
| chr1:145625801 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.415+2087T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625801 | |||||||
| chr1:145625827 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.415+2113A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625827 | |||||||
| chr1:145625911 | C | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+2197C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625911 | |||||||
| chr1:145625912 | C | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+2198C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145625912 | |||||||
| chr1:145626086 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+2372A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626086 | |||||||
| chr1:145626174 | T | C | 1 | a0001c0002t0001g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.415+2460T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626174 | |||||||
| chr1:145626179 | C | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+2465C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626179 | |||||||
| chr1:145626247 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.415+2533A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626247 | |||||||
| chr1:145626673 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+2959G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626673 | |||||||
| chr1:145626678 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.415+2964G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626678 | |||||||
| chr1:145626850 | G | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG02622.hp1 HG03579.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+3136G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626850 | |||||||
| chr1:145626889 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0148 others(9): Show |
13 | HG00438.hp2 HG00673.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.415+3175G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626889 | |||||||
| chr1:145626947 | T | TC | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.415+3233_415+3234i others(3): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626947 | |||||||
| chr1:145626947 | T | TCA | 3 | a0001c0001t0001g0034 a0001c0001t0001g0099 a0001c0001t0004g0042 |
3 | NA18978.hp2 NA18980.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.415+3233_415+3234i others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626947 | |||||||
| chr1:145626948 | A | C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0236 a0001c0002t0001g0023 others(11): Show |
14 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+3234A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626948 | |||||||
| chr1:145626962 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0108 a0001c0001t0001g0109 |
4 | HG03041.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+3248A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626962 | |||||||
| chr1:145627000 | T | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+3286T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145627000 | |||||||
| chr1:145627025 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.415+3311G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145627025 | |||||||
| chr1:145627098 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+3384G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145627098 | |||||||
| chr1:145627157 | T | C | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.415+3443T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145627157 | |||||||
| chr1:145627270 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.416-3417A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145627270 | |||||||
| chr1:145627680 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.416-3007T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145627680 | |||||||
| chr1:145627862 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-2825G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145627862 | |||||||
| chr1:145628250 | A | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.416-2437A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145628250 | |||||||
| chr1:145628399 | A | C | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.416-2288A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145628399 | |||||||
| chr1:145628472 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.416-2215G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145628472 | |||||||
| chr1:145628864 | A | C | 4 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-1823A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145628864 | |||||||
| chr1:145628956 | C | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0093 |
3 | HG01123.hp2 HG04199.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.416-1731C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145628956 | |||||||
| chr1:145628996 | A | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-1691A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145628996 | |||||||
| chr1:145629175 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.416-1512G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145629175 | |||||||
| chr1:145629198 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.416-1489G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145629198 | |||||||
| chr1:145629227 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.416-1460C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145629227 | |||||||
| chr1:145629294 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.416-1393G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145629294 | |||||||
| chr1:145629513 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.416-1174A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145629513 | |||||||
| chr1:145629922 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.416-765G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145629922 | |||||||
| chr1:145630254 | A | G | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG00099.hp2 HG00733.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-433A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145630254 | |||||||
| chr1:145630341 | G | GT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.416-333dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 145630341 | ||||||
| chr1:145630496 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.416-191G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145630496 | |||||||
| chr1:145630542 | C | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-145C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145630542 | |||||||
| chr1:145631086 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
134 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.536+279A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 6/13 | chr1 | 145631086 | |||||||
| chr1:145631352 | G | C | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.537-312G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 6/13 | chr1 | 145631352 | |||||||
| chr1:145631988 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18945.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.617+244C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145631988 | |||||||
| chr1:145632027 | T | A | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+283T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145632027 | |||||||
| chr1:145632233 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.617+489T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145632233 | |||||||
| chr1:145632608 | G | T | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+864G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145632608 | |||||||
| chr1:145632812 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0077 others(5): Show |
9 | HG02622.hp1 HG03041.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.617+1068A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145632812 | |||||||
| chr1:145632941 | T | C | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+1197T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145632941 | |||||||
| chr1:145633454 | G | A | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+1710G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633454 | |||||||
| chr1:145633521 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
10 | HG00140.hp2 HG00738.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+1777C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633521 | |||||||
| chr1:145633548 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+1804A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633548 | |||||||
| chr1:145633734 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.617+1990G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633734 | |||||||
| chr1:145633793 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.617+2049A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633793 | |||||||
| chr1:145633821 | G | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0231 a0001c0001t0001g0232 others(5): Show |
9 | HG02074.hp1 NA18941.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.617+2077G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633821 | |||||||
| chr1:145633848 | A | C | 3 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0091 |
3 | HG02257.hp1 HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.617+2104A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633848 | |||||||
| chr1:145633942 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.617+2198G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633942 | |||||||
| chr1:145633996 | T | A | 13 | a0001c0001t0001g0175 a0001c0002t0001g0023 a0001c0002t0001g0024 others(10): Show |
13 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.617+2252T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633996 | |||||||
| chr1:145633998 | T | G | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.617+2254T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145633998 | |||||||
| chr1:145634027 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.617+2283C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634027 | |||||||
| chr1:145634029 | C | T | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.617+2285C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634029 | |||||||
| chr1:145634057 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.617+2313A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634057 | |||||||
| chr1:145634081 | G | GTT | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(102): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.617+2352_617+2353d others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145634081 | ||||||
| chr1:145634175 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.617+2431G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634175 | |||||||
| chr1:145634178 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.617+2434T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634178 | |||||||
| chr1:145634261 | G | A | 1 | a0001c0001t0001g0007 | 2 | NA19003.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.617+2517G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634261 | |||||||
| chr1:145634307 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.617+2563C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634307 | |||||||
| chr1:145634320 | A | T | 1 | a0001c0001t0001g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.617+2576A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634320 | |||||||
| chr1:145634470 | A | G | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+2726A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634470 | |||||||
| chr1:145634473 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.617+2729A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634473 | |||||||
| chr1:145634631 | A | C | 16 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0040 others(13): Show |
17 | HG00609.hp2 HG02027.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.617+2887A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634631 | |||||||
| chr1:145635061 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG01175.hp2 HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.617+3317T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145635061 | |||||||
| chr1:145635178 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.617+3434G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145635178 | |||||||
| chr1:145635234 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.617+3490A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145635234 | |||||||
| chr1:145635279 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.617+3535G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145635279 | |||||||
| chr1:145635412 | G | GAA | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.617+3676_617+3677d others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145635412 | ||||||
| chr1:145635413 | A | AAC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0099 others(3): Show |
10 | HG00423.hp2 HG01975.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+3670_617+3671i others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145635413 | ||||||
| chr1:145635428 | T | TAAA | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+3684_617+3685i others(5): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145635428 | |||||||
| chr1:145635485 | G | C | 1 | a0001c0001t0001g0205 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.617+3741G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145635485 | |||||||
| chr1:145635908 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.617+4164G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145635908 | |||||||
| chr1:145635998 | T | G | 16 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(13): Show |
16 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.617+4254T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145635998 | |||||||
| chr1:145636124 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.617+4380A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145636124 | |||||||
| chr1:145636292 | A | G | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+4548A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145636292 | |||||||
| chr1:145636312 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.617+4568A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145636312 | |||||||
| chr1:145636644 | C | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+4900C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145636644 | |||||||
| chr1:145636735 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+4991A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145636735 | |||||||
| chr1:145636831 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.617+5087T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145636831 | |||||||
| chr1:145637093 | G | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+5349G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145637093 | |||||||
| chr1:145637545 | C | G | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.617+5801C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145637545 | |||||||
| chr1:145637597 | C | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+5853C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145637597 | |||||||
| chr1:145638041 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.618-5828C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145638041 | |||||||
| chr1:145638110 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.618-5759T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145638110 | |||||||
| chr1:145638201 | G | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0179 a0001c0002t0001g0023 others(11): Show |
15 | HG01070.hp2 HG01074.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.618-5668G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145638201 | |||||||
| chr1:145638536 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.618-5333A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145638536 | |||||||
| chr1:145638539 | T | G | 14 | a0001c0001t0001g0103 a0001c0001t0001g0245 a0001c0002t0001g0023 others(11): Show |
14 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.618-5330T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145638539 | |||||||
| chr1:145638776 | G | GA | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.618-5084dupA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145638776 | ||||||
| chr1:145638940 | A | C | 13 | a0001c0001t0001g0103 a0001c0002t0001g0023 a0001c0002t0001g0024 others(10): Show |
13 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.618-4929A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145638940 | |||||||
| chr1:145639062 | ATACT | A | 12 | a0001c0001t0001g0103 a0001c0002t0001g0023 a0001c0002t0001g0024 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.618-4803_618-4800d others(6): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145639062 | ||||||
| chr1:145639333 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.618-4536A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639333 | |||||||
| chr1:145639390 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-4479A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639390 | |||||||
| chr1:145639457 | C | T | 3 | a0001c0003t0001g0111 a0001c0003t0001g0112 a0001c0003t0001g0113 |
3 | NA18985.hp1 NA19058.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.618-4412C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639457 | |||||||
| chr1:145639475 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-4394A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639475 | |||||||
| chr1:145639486 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.618-4383T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639486 | |||||||
| chr1:145639663 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-4206T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639663 | |||||||
| chr1:145639707 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-4162C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639707 | |||||||
| chr1:145639734 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-4135A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639734 | |||||||
| chr1:145639746 | C | CA | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.618-4109dupA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145639746 | ||||||
| chr1:145639746 | C | CAA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0094 a0001c0002t0001g0023 others(11): Show |
15 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.618-4110_618-4109d others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145639746 | ||||||
| chr1:145639791 | C | G | 4 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-4078C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639791 | |||||||
| chr1:145639820 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.618-4049G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639820 | |||||||
| chr1:145639821 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.618-4048C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639821 | |||||||
| chr1:145639940 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-3929G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639940 | |||||||
| chr1:145639945 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-3924T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145639945 | |||||||
| chr1:145640029 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-3840C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640029 | |||||||
| chr1:145640046 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-3823C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640046 | |||||||
| chr1:145640060 | A | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0146 a0001c0001t0001g0188 others(5): Show |
9 | HG00609.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.618-3809A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640060 | |||||||
| chr1:145640113 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-3756A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640113 | |||||||
| chr1:145640272 | G | GA | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.618-3585dupA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145640272 | ||||||
| chr1:145640420 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-3449G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640420 | |||||||
| chr1:145640514 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-3355G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640514 | |||||||
| chr1:145640563 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.618-3306C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640563 | |||||||
| chr1:145640627 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-3242A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640627 | |||||||
| chr1:145640691 | TA | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.618-3177delA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640691 | |||||||
| chr1:145640692 | A | C | 2 | a0001c0001t0001g0044 a0001c0002t0001g0138 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.618-3177A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640692 | |||||||
| chr1:145640693 | C | T | 2 | a0001c0001t0001g0044 a0001c0002t0001g0138 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.618-3176C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640693 | |||||||
| chr1:145640695 | T | A | 2 | a0001c0001t0001g0044 a0001c0002t0001g0138 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.618-3174T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640695 | |||||||
| chr1:145640695 | T | TAA | 26 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0041 others(23): Show |
26 | HG00323.hp1 HG01256.hp1 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.618-3158_618-3157d others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145640695 | ||||||
| chr1:145640695 | T | TAAA | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.618-3159_618-3157d others(5): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145640695 | ||||||
| chr1:145640695 | T | TAAAA | 10 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0146 others(7): Show |
11 | HG00609.hp1 HG00741.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-3160_618-3157d others(6): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145640695 | ||||||
| chr1:145640713 | T | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.618-3156T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640713 | |||||||
| chr1:145640847 | A | C | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.618-3022A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640847 | |||||||
| chr1:145640882 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-2987G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640882 | |||||||
| chr1:145641052 | G | A | 2 | a0001c0001t0001g0103 a0001c0002t0001g0138 |
2 | HG02683.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.618-2817G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641052 | |||||||
| chr1:145641193 | CA | C | 13 | a0001c0001t0001g0103 a0001c0002t0001g0023 a0001c0002t0001g0024 others(10): Show |
13 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.618-2669delA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145641193 | ||||||
| chr1:145641324 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.618-2545T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641324 | |||||||
| chr1:145641335 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-2534A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641335 | |||||||
| chr1:145641398 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0232 a0001c0001t0001g0233 others(3): Show |
7 | HG02074.hp1 NA18941.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-2471T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641398 | |||||||
| chr1:145641514 | C | T | 13 | a0001c0001t0001g0103 a0001c0002t0001g0023 a0001c0002t0001g0024 others(10): Show |
13 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.618-2355C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641514 | |||||||
| chr1:145641571 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0074 |
3 | HG00733.hp1 HG00741.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.618-2298A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641571 | |||||||
| chr1:145641582 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0108 a0001c0001t0001g0109 |
4 | HG03041.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-2287G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641582 | |||||||
| chr1:145641670 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-2199G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641670 | |||||||
| chr1:145641922 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-1947G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145641922 | |||||||
| chr1:145642294 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-1575A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145642294 | |||||||
| chr1:145642553 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-1316T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145642553 | |||||||
| chr1:145642627 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-1242G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145642627 | |||||||
| chr1:145642833 | A | C | 17 | a0001c0001t0001g0103 a0001c0001t0001g0239 a0001c0001t0001g0241 others(14): Show |
17 | HG00609.hp1 HG02040.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.618-1036A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145642833 | |||||||
| chr1:145642962 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-907T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145642962 | |||||||
| chr1:145642985 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-884G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145642985 | |||||||
| chr1:145643136 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.618-733A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145643136 | |||||||
| chr1:145643150 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-719G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145643150 | |||||||
| chr1:145643226 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-643T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145643226 | |||||||
| chr1:145643457 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-412C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145643457 | |||||||
| chr1:145643533 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-336C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145643533 | |||||||
| chr1:145643534 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-335A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145643534 | |||||||
| chr1:145643587 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-282G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145643587 | |||||||
| chr1:145643701 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.618-168A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145643701 | |||||||
| chr1:145644093 | C | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0074 |
3 | HG00733.hp1 HG00741.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.727+115C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145644093 | |||||||
| chr1:145644169 | G | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | NA18990.hp2 NA18999.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.727+191G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145644169 | |||||||
| chr1:145644470 | T | C | 13 | a0001c0001t0001g0103 a0001c0002t0001g0023 a0001c0002t0001g0024 others(10): Show |
13 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.727+492T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145644470 | |||||||
| chr1:145644494 | C | T | 4 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+516C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145644494 | |||||||
| chr1:145644499 | C | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.727+521C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145644499 | |||||||
| chr1:145644713 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.727+735C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145644713 | |||||||
| chr1:145644983 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.727+1005T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145644983 | |||||||
| chr1:145645004 | T | A | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.727+1026T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145645004 | |||||||
| chr1:145645262 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.728-922G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145645262 | |||||||
| chr1:145645401 | A | G | 4 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0211 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-783A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145645401 | |||||||
| chr1:145645740 | G | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.728-444G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 8/13 | chr1 | 145645740 | |||||||
| chr1:145646523 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.816+251G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 9/13 | chr1 | 145646523 | |||||||
| chr1:145646727 | A | C | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.817-448A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 9/13 | chr1 | 145646727 | |||||||
| chr1:145646932 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.817-243G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 9/13 | chr1 | 145646932 | |||||||
| chr1:145647273 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0216 |
2 | HG02602.hp1 HG03831.hp2 |
splice_region_variant&intron_variant | LOW | c.909+6T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647273 | |||||||
| chr1:145647289 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.909+22A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647289 | |||||||
| chr1:145647426 | C | A | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.909+159C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647426 | |||||||
| chr1:145647459 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.909+192G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647459 | |||||||
| chr1:145647730 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0075 others(9): Show |
13 | HG01123.hp2 HG02622.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+463G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647730 | |||||||
| chr1:145647737 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.909+470G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647737 | |||||||
| chr1:145647765 | A | T | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.909+498A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647765 | |||||||
| chr1:145647808 | TCTCTCTT others(35): Show |
T | 1 | a0001c0002t0005g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.909+548_909+589del others(42): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647808 | ||||||
| chr1:145647810 | TCTCTTCG others(10): Show |
T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
27 | HG00621.hp1 HG00621.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.909+548_909+564del others(17): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647810 | ||||||
| chr1:145647812 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.909+545T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647812 | |||||||
| chr1:145647812 | TCTTCGTC others(8): Show |
T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(35): Show |
43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.909+548_909+562del others(15): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647812 | ||||||
| chr1:145647812 | TCTTCGTC others(31): Show |
T | 3 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0027 |
3 | HG03195.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.909+548_909+585del others(38): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647812 | ||||||
| chr1:145647814 | TTCGTCGT others(6): Show |
T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(42): Show |
48 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.909+548_909+560del others(13): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647814 | |||||||
| chr1:145647814 | TTCGTCGT others(21): Show |
T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0088 others(16): Show |
20 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.909+550_909+577del others(28): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647814 | ||||||
| chr1:145647814 | TTCGTCGT others(24): Show |
T | 1 | a0001c0001t0001g0173 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.909+550_909+580del others(31): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647814 | ||||||
| chr1:145647814 | TTCGTCGT others(27): Show |
T | 1 | a0001c0001t0001g0114 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.909+550_909+583del others(34): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647814 | ||||||
| chr1:145647814 | TTCGTCGT others(29): Show |
T | 3 | a0001c0002t0001g0025 a0001c0002t0001g0029 a0001c0002t0002g0135 |
3 | HG02717.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.909+548_909+583del others(36): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647814 | |||||||
| chr1:145647815 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.909+548T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647815 | |||||||
| chr1:145647816 | CGTCGTCG others(4): Show |
C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
69 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.909+550_909+560del others(11): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647816 | |||||||
| chr1:145647817 | G | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(50): Show |
54 | HG00280.hp1 HG00733.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.909+550G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647817 | |||||||
| chr1:145647817 | G | T | 2 | a0001c0002t0001g0021 a0001c0002t0001g0022 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.909+550G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647817 | |||||||
| chr1:145647818 | T | C | 2 | a0001c0002t0001g0021 a0001c0002t0001g0022 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.909+551T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647818 | |||||||
| chr1:145647819 | CGTCGTCG | C | 9 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0145 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.909+553_909+559del others(7): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647819 | |||||||
| chr1:145647819 | CGTCGTCG others(3): Show |
C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0200 |
3 | HG01074.hp2 HG01168.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.909+553_909+562del others(10): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647819 | |||||||
| chr1:145647819 | CGTCGTCG others(5): Show |
C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0166 |
2 | HG01433.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.909+553_909+564del others(12): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647819 | |||||||
| chr1:145647819 | CGTCGTCG others(7): Show |
C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0143 others(3): Show |
6 | HG02145.hp2 HG03831.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+553_909+566del others(14): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647819 | |||||||
| chr1:145647819 | CGTCGTCG others(9): Show |
C | 1 | a0001c0003t0001g0113 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.909+553_909+568del others(16): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647819 | |||||||
| chr1:145647819 | CGTCGTCG others(20): Show |
C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0030 others(18): Show |
22 | HG00733.hp2 HG01167.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.909+553_909+579del others(27): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647819 | |||||||
| chr1:145647819 | CGTCGTCG others(23): Show |
C | 8 | a0001c0001t0001g0084 a0001c0001t0001g0096 a0001c0001t0001g0155 others(5): Show |
8 | HG00280.hp1 HG01884.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+553_909+582del others(30): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647819 | |||||||
| chr1:145647820 | G | C | 2 | a0001c0002t0001g0021 a0001c0002t0001g0022 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.909+553G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647820 | |||||||
| chr1:145647823 | G | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.909+556G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647823 | |||||||
| chr1:145647826 | G | C | 2 | a0001c0002t0001g0021 a0001c0002t0001g0022 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.909+559G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647826 | |||||||
| chr1:145647827 | A | C | 9 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0145 others(6): Show |
9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.909+560A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647827 | |||||||
| chr1:145647827 | A | T | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+560A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647827 | |||||||
| chr1:145647829 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.909+562T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647829 | |||||||
| chr1:145647831 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.909+564T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647831 | |||||||
| chr1:145647833 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(64): Show |
71 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.909+566T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647833 | |||||||
| chr1:145647835 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(35): Show |
43 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.909+568T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647835 | |||||||
| chr1:145647837 | T | C | 24 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0033 others(21): Show |
25 | HG00621.hp1 HG00621.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.909+570T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647837 | |||||||
| chr1:145647843 | T | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0088 others(16): Show |
20 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.909+576T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647843 | |||||||
| chr1:145647843 | TCCTCCTC | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.909+578_909+584del others(7): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647843 | ||||||
| chr1:145647844 | C | CT | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+577_909+578ins others(1): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647844 | |||||||
| chr1:145647844 | CCTCCT | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0049 others(8): Show |
11 | HG01074.hp1 HG01099.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+579_909+583del others(5): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647844 | ||||||
| chr1:145647846 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.909+579T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647846 | |||||||
| chr1:145647848 | C | T | 3 | a0001c0001t0001g0129 a0001c0002t0001g0019 a0001c0002t0001g0021 |
3 | HG02922.hp1 HG03225.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.909+581C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647848 | |||||||
| chr1:145647849 | T | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0088 others(20): Show |
24 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.909+582T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647849 | |||||||
| chr1:145647850 | C | CT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0030 others(20): Show |
24 | HG00733.hp2 HG01167.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.909+583_909+584ins others(1): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647850 | |||||||
| chr1:145647850 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(31): Show |
35 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.909+583C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647850 | |||||||
| chr1:145647854 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.909+587T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647854 | |||||||
| chr1:145647865 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.909+598C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647865 | |||||||
| chr1:145647869 | C | A | 1 | a0001c0001t0001g0049 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.909+602C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647869 | |||||||
| chr1:145647871 | C | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0081 |
2 | NA18947.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.909+604C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647871 | |||||||
| chr1:145647873 | C | A | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0075 others(4): Show |
7 | HG02630.hp2 HG03688.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+606C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647873 | |||||||
| chr1:145647875 | C | A | 14 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0050 others(11): Show |
14 | HG02027.hp1 HG02055.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.909+608C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647875 | |||||||
| chr1:145647877 | C | A | 26 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0044 others(23): Show |
26 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.909+610C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647877 | |||||||
| chr1:145647879 | C | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0035 others(45): Show |
51 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.909+612C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647879 | |||||||
| chr1:145647879 | CTATA | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
39 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.909+641_909+644del others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647879 | ||||||
| chr1:145647879 | CTATATA | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0018 others(30): Show |
35 | HG00323.hp1 HG00609.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.909+639_909+644del others(6): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647879 | ||||||
| chr1:145647879 | CTATATAT others(1): Show |
C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0057 others(19): Show |
24 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.909+637_909+644del others(8): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647879 | ||||||
| chr1:145647879 | CTATATAT others(3): Show |
C | 10 | a0001c0001t0001g0098 a0001c0001t0001g0161 a0001c0001t0001g0171 others(7): Show |
10 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.909+635_909+644del others(10): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145647879 | ||||||
| chr1:145647881 | A | C | 63 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(60): Show |
67 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.909+614A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647881 | |||||||
| chr1:145647883 | A | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0064 a0001c0001t0001g0079 others(25): Show |
29 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.909+616A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647883 | |||||||
| chr1:145647885 | A | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0084 a0001c0001t0001g0096 others(15): Show |
19 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+618A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647885 | |||||||
| chr1:145647886 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.909+619T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647886 | |||||||
| chr1:145647887 | A | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0085 a0001c0001t0001g0145 others(8): Show |
12 | HG00323.hp1 HG01099.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+620A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647887 | |||||||
| chr1:145647889 | A | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0085 a0001c0001t0001g0142 others(6): Show |
9 | HG00280.hp1 HG01099.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.909+622A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647889 | |||||||
| chr1:145647891 | A | C | 3 | a0001c0001t0001g0161 a0001c0002t0002g0135 a0001c0004t0001g0082 |
3 | HG01884.hp2 HG02717.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.909+624A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647891 | |||||||
| chr1:145647893 | A | C | 1 | a0001c0002t0002g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.909+626A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647893 | |||||||
| chr1:145647922 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.909+655A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647922 | |||||||
| chr1:145648389 | G | T | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1122G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648389 | |||||||
| chr1:145648487 | C | CTTTT | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+1228_909+1231d others(6): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145648487 | ||||||
| chr1:145648512 | T | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+1245T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648512 | |||||||
| chr1:145648588 | T | C | 2 | a0001c0001t0001g0241 a0002c0005t0001g0242 |
2 | HG00609.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.909+1321T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648588 | |||||||
| chr1:145648641 | A | G | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+1374A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648641 | |||||||
| chr1:145648795 | G | GTC | 24 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0062 others(21): Show |
24 | HG00738.hp2 HG01175.hp2 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+1529_909+1530i others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145648795 | ||||||
| chr1:145648796 | T | TC | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.909+1529_909+1530i others(3): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648796 | |||||||
| chr1:145648817 | G | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.909+1550G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648817 | |||||||
| chr1:145648825 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.909+1558C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648825 | |||||||
| chr1:145648916 | TG | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+1650delG | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648916 | |||||||
| chr1:145648918 | C | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+1651C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648918 | |||||||
| chr1:145649047 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG02300.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.909+1780G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145649047 | |||||||
| chr1:145649223 | G | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | NA18990.hp2 NA18999.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.909+1956G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145649223 | |||||||
| chr1:145649316 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.909+2049C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145649316 | |||||||
| chr1:145649405 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.909+2138C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145649405 | |||||||
| chr1:145649552 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.909+2285A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145649552 | |||||||
| chr1:145649672 | G | T | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.909+2405G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145649672 | |||||||
| chr1:145650041 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.909+2774T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145650041 | |||||||
| chr1:145650070 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0205 |
2 | NA18978.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.909+2803C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145650070 | |||||||
| chr1:145650227 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.909+2960C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145650227 | |||||||
| chr1:145650306 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0216 |
2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.909+3039G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145650306 | |||||||
| chr1:145650597 | C | A | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+3330C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145650597 | |||||||
| chr1:145650637 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+3370G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145650637 | |||||||
| chr1:145650870 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+3603T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145650870 | |||||||
| chr1:145650879 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+3612G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145650879 | |||||||
| chr1:145651539 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+4272A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145651539 | |||||||
| chr1:145651614 | C | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+4347C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145651614 | |||||||
| chr1:145651847 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0055 |
2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.909+4580T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145651847 | |||||||
| chr1:145651889 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.909+4622C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145651889 | |||||||
| chr1:145651903 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0060 a0001c0001t0001g0063 |
3 | NA18944.hp1 NA18990.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.909+4636C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145651903 | |||||||
| chr1:145652146 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.909+4879C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652146 | |||||||
| chr1:145652203 | G | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0093 |
3 | HG01123.hp2 HG04199.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.909+4936G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652203 | |||||||
| chr1:145652208 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.909+4941G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652208 | |||||||
| chr1:145652254 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.909+4987C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652254 | |||||||
| chr1:145652301 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0055 |
2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.909+5034C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652301 | |||||||
| chr1:145652334 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0055 |
2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.909+5067T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652334 | |||||||
| chr1:145652338 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0055 |
2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.909+5071C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652338 | |||||||
| chr1:145652356 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+5089G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652356 | |||||||
| chr1:145652583 | C | CT | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+5317dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145652583 | ||||||
| chr1:145652585 | C | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+5318C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652585 | |||||||
| chr1:145652744 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.909+5477T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652744 | |||||||
| chr1:145652871 | C | CTTCTT | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+5605_909+5609d others(7): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145652871 | ||||||
| chr1:145652942 | AT | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0108 a0001c0001t0001g0109 |
4 | HG03041.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+5682delT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145652942 | ||||||
| chr1:145652955 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0220 |
3 | HG02109.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.909+5688G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652955 | |||||||
| chr1:145652964 | G | GT | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
153 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.909+5697_909+5698i others(3): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145652964 | |||||||
| chr1:145653022 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+5755G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653022 | |||||||
| chr1:145653285 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0086 |
2 | NA18982.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.909+6018T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653285 | |||||||
| chr1:145653390 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.909+6123G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653390 | |||||||
| chr1:145653612 | C | T | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+6345C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653612 | |||||||
| chr1:145653635 | T | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+6368T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653635 | |||||||
| chr1:145653648 | G | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.909+6381G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653648 | |||||||
| chr1:145653746 | C | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+6479C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653746 | |||||||
| chr1:145653953 | G | A | 44 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(41): Show |
45 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.909+6686G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653953 | |||||||
| chr1:145653954 | C | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+6687C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145653954 | |||||||
| chr1:145654182 | GA | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0179 a0001c0001t0001g0185 others(1): Show |
5 | HG01070.hp2 HG01074.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+6919delA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145654182 | ||||||
| chr1:145654194 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.909+6927A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654194 | |||||||
| chr1:145654417 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0114 |
3 | HG00423.hp1 HG00735.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.909+7150G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654417 | |||||||
| chr1:145654451 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.909+7184G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654451 | |||||||
| chr1:145654544 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.909+7277A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654544 | |||||||
| chr1:145654551 | T | TCA | 4 | a0001c0001t0001g0017 a0001c0001t0001g0078 a0001c0001t0001g0098 others(1): Show |
4 | HG01167.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+7284_909+7285i others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654551 | |||||||
| chr1:145654551 | T | TCAAA | 18 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0040 others(15): Show |
18 | HG00609.hp2 HG00673.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.909+7284_909+7285i others(6): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654551 | |||||||
| chr1:145654551 | T | TCAAAA | 8 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(5): Show |
8 | HG02055.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+7284_909+7285i others(7): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654551 | |||||||
| chr1:145654572 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.909+7305C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654572 | |||||||
| chr1:145654574 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.909+7307G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654574 | |||||||
| chr1:145654757 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.909+7490G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654757 | |||||||
| chr1:145654914 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+7647G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654914 | |||||||
| chr1:145655484 | G | T | 1 | a0001c0002t0002g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.910-7845G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145655484 | |||||||
| chr1:145655578 | C | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0001t0001g0108 others(13): Show |
17 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-7751C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145655578 | |||||||
| chr1:145655702 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0093 |
3 | HG01123.hp2 HG04199.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.910-7627C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145655702 | |||||||
| chr1:145656065 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.910-7264G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145656065 | |||||||
| chr1:145656133 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.910-7196A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145656133 | |||||||
| chr1:145656136 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-7193G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145656136 | |||||||
| chr1:145656336 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.910-6993C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145656336 | |||||||
| chr1:145656378 | C | G | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.910-6951C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145656378 | |||||||
| chr1:145656629 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.910-6700G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145656629 | |||||||
| chr1:145656808 | T | TTTCA | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-6519_910-6518i others(6): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145656808 | ||||||
| chr1:145657073 | G | T | 1 | a0001c0001t0001g0014 | 2 | HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.910-6256G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145657073 | |||||||
| chr1:145657093 | T | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0121 others(11): Show |
16 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.910-6236T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145657093 | |||||||
| chr1:145657191 | T | C | 44 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0046 others(41): Show |
44 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.910-6138T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145657191 | |||||||
| chr1:145657211 | T | C | 29 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
32 | HG00609.hp1 HG01175.hp2 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.910-6118T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145657211 | |||||||
| chr1:145657348 | A | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0066 others(33): Show |
39 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.910-5981A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145657348 | |||||||
| chr1:145657606 | C | T | 2 | a0001c0002t0001g0026 a0001c0002t0001g0027 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.910-5723C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145657606 | |||||||
| chr1:145657636 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.910-5693G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145657636 | |||||||
| chr1:145657784 | C | T | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-5545C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145657784 | |||||||
| chr1:145658479 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.910-4850T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145658479 | |||||||
| chr1:145658550 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.910-4779G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145658550 | |||||||
| chr1:145658566 | C | G | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.910-4763C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145658566 | |||||||
| chr1:145659224 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0147 a0001c0001t0001g0193 others(1): Show |
4 | HG02074.hp2 NA18973.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-4105G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145659224 | |||||||
| chr1:145659481 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.910-3848G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145659481 | |||||||
| chr1:145659562 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.910-3767C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145659562 | |||||||
| chr1:145659928 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.910-3401G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145659928 | |||||||
| chr1:145659987 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-3342A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145659987 | |||||||
| chr1:145660033 | A | G | 1 | a0001c0002t0001g0023 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.910-3296A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660033 | |||||||
| chr1:145660297 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0092 |
3 | HG02027.hp1 HG02135.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.910-3032T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660297 | |||||||
| chr1:145660324 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.910-3005C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660324 | |||||||
| chr1:145660470 | T | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-2859T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660470 | |||||||
| chr1:145660626 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.910-2703C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660626 | |||||||
| chr1:145660640 | G | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.910-2689G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660640 | |||||||
| chr1:145660641 | C | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.910-2688C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660641 | |||||||
| chr1:145660642 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0240 |
2 | NA18969.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.910-2687G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660642 | |||||||
| chr1:145660676 | T | A | 7 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(4): Show |
7 | HG02922.hp2 HG03195.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-2653T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660676 | |||||||
| chr1:145660683 | C | A | 7 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(4): Show |
7 | HG02922.hp2 HG03195.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-2646C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660683 | |||||||
| chr1:145660783 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2546A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660783 | |||||||
| chr1:145660820 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2509G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660820 | |||||||
| chr1:145660833 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2496C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660833 | |||||||
| chr1:145660879 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2450C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660879 | |||||||
| chr1:145660904 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2425T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660904 | |||||||
| chr1:145660919 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2410C>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660919 | |||||||
| chr1:145660955 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2374G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660955 | |||||||
| chr1:145660972 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2357C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660972 | |||||||
| chr1:145660983 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2346G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660983 | |||||||
| chr1:145660995 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.910-2334A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145660995 | |||||||
| chr1:145661004 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2325C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661004 | |||||||
| chr1:145661007 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2322G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661007 | |||||||
| chr1:145661029 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2300G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661029 | |||||||
| chr1:145661070 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2259T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661070 | |||||||
| chr1:145661071 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2258G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661071 | |||||||
| chr1:145661092 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.910-2237G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661092 | |||||||
| chr1:145661125 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2204C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661125 | |||||||
| chr1:145661126 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2203A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661126 | |||||||
| chr1:145661158 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2171G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661158 | |||||||
| chr1:145661171 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.910-2158T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661171 | |||||||
| chr1:145661202 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-2127A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661202 | |||||||
| chr1:145661260 | A | G | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-2069A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661260 | |||||||
| chr1:145661319 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.910-2010G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661319 | |||||||
| chr1:145661324 | G | T | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.910-2005G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661324 | |||||||
| chr1:145661449 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.910-1880A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661449 | |||||||
| chr1:145661756 | G | C | 1 | a0001c0001t0001g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.910-1573G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661756 | |||||||
| chr1:145661775 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-1554G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661775 | |||||||
| chr1:145661802 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-1527G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145661802 | |||||||
| chr1:145662130 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.910-1199T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145662130 | |||||||
| chr1:145662132 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.910-1197C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145662132 | |||||||
| chr1:145662172 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.910-1157T>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145662172 | |||||||
| chr1:145662190 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0195 |
2 | HG03492.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.910-1139G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145662190 | |||||||
| chr1:145663165 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
134 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.910-164A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145663165 | |||||||
| chr1:145663242 | C | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-87C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145663242 | |||||||
| chr1:145664277 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1005+853A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145664277 | |||||||
| chr1:145664323 | ATCTTT | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0211 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+904_1005+908d others(7): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 145664323 | ||||||
| chr1:145664504 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1006-1058G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145664504 | |||||||
| chr1:145664574 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1006-988G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145664574 | |||||||
| chr1:145664591 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1006-971A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145664591 | |||||||
| chr1:145664836 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
12 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006-726G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145664836 | |||||||
| chr1:145664876 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1006-686T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145664876 | |||||||
| chr1:145664945 | G | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0065 |
3 | HG01081.hp1 HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1006-617G>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145664945 | |||||||
| chr1:145665267 | G | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0115 |
2 | HG00735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1006-295G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145665267 | |||||||
| chr1:145665360 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG00099.hp2 HG00733.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1006-202G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145665360 | |||||||
| chr1:145665393 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1006-169G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 11/13 | chr1 | 145665393 | |||||||
| chr1:145665926 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1095+275A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145665926 | |||||||
| chr1:145665940 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1095+289A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145665940 | |||||||
| chr1:145666371 | A | C | 1 | a0001c0002t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1095+720A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145666371 | |||||||
| chr1:145666488 | A | G | 1 | a0001c0004t0001g0082 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1095+837A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145666488 | |||||||
| chr1:145666509 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(8): Show |
11 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1095+858G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145666509 | |||||||
| chr1:145666565 | A | T | 13 | a0001c0001t0001g0224 a0001c0002t0001g0023 a0001c0002t0001g0024 others(10): Show |
13 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1095+914A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145666565 | |||||||
| chr1:145666822 | C | T | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1095+1171C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145666822 | |||||||
| chr1:145666873 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1095+1222G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145666873 | |||||||
| chr1:145666895 | G | A | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1095+1244G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145666895 | |||||||
| chr1:145666943 | C | T | 1 | a0001c0002t0002g0137 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1095+1292C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145666943 | |||||||
| chr1:145667155 | T | C | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1095+1504T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145667155 | |||||||
| chr1:145667231 | A | C | 4 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+1580A>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145667231 | |||||||
| chr1:145667517 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0148 others(9): Show |
13 | HG00438.hp2 HG00673.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1095+1866A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145667517 | |||||||
| chr1:145667619 | C | T | 2 | a0001c0001t0001g0071 a0001c0002t0001g0138 |
2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1095+1968C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145667619 | |||||||
| chr1:145667981 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1096-1644A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145667981 | |||||||
| chr1:145668146 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1096-1479A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145668146 | |||||||
| chr1:145668183 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1096-1442T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145668183 | |||||||
| chr1:145668613 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1096-1012A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145668613 | |||||||
| chr1:145668629 | A | T | 1 | a0001c0002t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1096-996A>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145668629 | |||||||
| chr1:145668741 | G | A | 3 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0091 |
3 | HG02257.hp1 HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1096-884G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145668741 | |||||||
| chr1:145668895 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1096-730C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145668895 | |||||||
| chr1:145668955 | C | T | 1 | a0001c0001t0001g0008 | 2 | NA18965.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1096-670C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145668955 | |||||||
| chr1:145669604 | C | T | 12 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(9): Show |
12 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096-21C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 12/13 | chr1 | 145669604 | |||||||
| chr1:145669718 | T | G | 1 | a0001c0001t0001g0015 | 2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1161+28T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 13/13 | chr1 | 145669718 |