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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 455 | 273 | 74 | 46 | 111 | 10 | 30 | 82 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0002 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1368 | 253 | 57 | 46 | 108 | 10 | 30 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
c0002 | 0/0 | 1368 | 16 | 16 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
c0003 | 0/0 | 1368 | 3 | 0 | 0 | 3 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
c0004 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
c0005 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 757 | 264 | 66 | 46 | 110 | 10 | 30 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
t0002 | 0/0 | 757 | 4 | 4 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
t0003 | 0/0 | 757 | 3 | 3 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
t0004 | 0/0 | 757 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
t0005 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
t0006 | 0/0 | 757 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1368 | 253 | 57 | 46 | 108 | 10 | 30 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0002 | 0/0 | 1368 | 16 | 16 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0003 | 0/0 | 1368 | 3 | 0 | 0 | 3 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0004 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0002c0005 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | 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 | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0001t0003 | 0/0 | 2124 | 3 | 3 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0001t0004 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0001t0006 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0002t0001 | 0/0 | 2124 | 11 | 11 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0002t0002 | 0/0 | 2124 | 4 | 4 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0002t0005 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0003t0001 | 0/0 | 2124 | 3 | 0 | 0 | 3 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0001c0004t0001 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
a0002c0005t0001 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | copy fasta | chr1 | 145602988 | 145675650 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | 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 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1/0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0242 | 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 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0001t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
a0002c0005t0001g0255 | 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 | g0045 | EUR | GBR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | FIN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00609 | hp1 | a0002 | c0005 | t0001 | g0255 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0181 | 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 | g0012 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0072 | 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 | g0188 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0190 | 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 | g0198 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0089 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0143 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0223 | 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 | g0224 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0144 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0141 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0024 | 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 | g0170 | EAS | CHB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18985 | hp1 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19030 | hp1 | a0001 | c0002 | t0005 | g0025 | AFR | LWK | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19058 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | YRI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ASW | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ASW | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | USA | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0063 | REF | REF | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0149 | REF | REF | GPR89A_chr1_145602988_145675650 | GPR89A | chr1 | 145602988 | 145675650 |
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 |
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 |
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 |
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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0257 | 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 | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 153 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(150): 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 | a0001c0002t0001g0145a0001c0002t0002g0141a0001c0002t0002g0142others(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 | a0001c0001t0001g0139a0001c0001t0001g0140 | 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 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(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 | a0001c0002t0001g0145a0001c0002t0002g0141a0001c0002t0002g0142others(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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0137 | 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 | 20 | a0001c0001t0001g0013a0001c0001t0001g0233a0001c0001t0001g0234others(17): 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 | a0001c0002t0001g0145a0001c0002t0002g0141a0001c0002t0002g0142others(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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | a0001c0001t0001g0232 | 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 | a0001c0002t0001g0145a0001c0002t0002g0141a0001c0002t0002g0142others(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 | a0001c0001t0001g0136 | 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 | a0001c0002t0001g0145a0001c0002t0002g0141a0001c0002t0002g0142others(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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0125others(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 | a0001c0002t0002g0141a0001c0002t0002g0142a0001c0002t0002g0143others(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 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(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 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120 | 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 | a0001c0002t0001g0145a0001c0002t0002g0141a0001c0002t0002g0142others(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 | a0001c0001t0001g0146a0001c0001t0001g0147 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0116 | 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 | a0001c0001t0001g0114 | 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 | 13 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0104others(10): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 141 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(138): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | ||||||
chr1:145611686
|
A | AT | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.42+3521dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 145611686 | |||||
chr1:145611762
|
G | A | 12 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0228 | 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 | a0001c0003t0001g0119a0001c0003t0001g0120 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0029a0001c0001t0001g0030 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0150 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0145 | 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 | a0002c0005t0001g0255 | 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 | a0001c0001t0001g0258 | 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 | a0001c0002t0002g0141a0001c0002t0002g0142a0001c0002t0002g0143others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0100 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0151 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.43-747G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | chr1 | 145615487 | ||||||
chr1:145615634
|
C | CT | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.43-592dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 145615634 | |||||
chr1:145615662
|
A | G | 1 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0138 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0099 | 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 | a0001c0001t0001g0226 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0136 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0002t0001g0020others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0113 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.103-25C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 2/13 | chr1 | 145618295 | ||||||
chr1:145618506
|
G | GA | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.206+93dupA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 145618506 | |||||
chr1:145618633
|
C | T | 1 | a0001c0001t0001g0136 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0034a0001c0001t0001g0035 | 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 | a0001c0001t0001g0224a0001c0001t0001g0228 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.206+894G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145619317 | ||||||
chr1:145619318
|
A | AAG | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(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 | a0001c0001t0001g0223 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0092a0001c0001t0001g0250 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0250a0001c0002t0001g0145 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0224a0001c0001t0001g0228 | 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 | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(151): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0152a0001c0001t0001g0153 | 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 | a0001c0001t0001g0034 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0036 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.207-1534T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | chr1 | 145621520 | ||||||
chr1:145621908
|
C | CA | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.207-1136dupA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 145621908 | |||||
chr1:145622353
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 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 | a0001c0001t0001g0031 | 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 | a0001c0002t0001g0023a0001c0002t0001g0024 | 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 | a0001c0001t0001g0235 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0090 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0117 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0010a0001c0001t0001g0148a0001c0001t0001g0151others(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 | a0001c0001t0001g0155 | 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 | a0001c0002t0001g0145 | 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 | 11 | a0001c0001t0001g0011a0001c0001t0001g0146a0001c0001t0001g0147others(8): 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 | ||||||
chr1:145625343
|
C | CTT | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.415+1639_415+1640d others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 145625343 | |||||
chr1:145625500
|
C | T | 1 | a0001c0004t0001g0089 | 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 | a0001c0001t0001g0111 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0088 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0016 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0111 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0014a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0001g0010a0001c0001t0001g0148a0001c0001t0001g0156others(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 | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0001g0031a0001c0001t0001g0105a0001c0001t0004g0041 | 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 | a0001c0001t0001g0034a0001c0001t0001g0249a0001c0002t0001g0020others(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 | ||||||
chr1:145626949
|
C | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.415+3235C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 5/13 | chr1 | 145626949 | ||||||
chr1:145626962
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0116 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0136 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0042 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0187 | 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 | a0001c0002t0002g0141a0001c0002t0002g0142a0001c0002t0002g0143others(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 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0100 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0156 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0139a0001c0001t0001g0140 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(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 | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 135 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(132): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18945.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.617+244C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145631988 | ||||||
chr1:145632021
|
T | TA | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.617+282dupA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145632021 | |||||
chr1:145632027
|
T | A | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | a0001c0001t0001g0219 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0084others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | 9 | a0001c0001t0001g0011a0001c0001t0001g0146a0001c0001t0001g0147others(6): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): 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 | a0001c0001t0001g0081 | 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 | 9 | a0001c0001t0001g0013a0001c0001t0001g0243a0001c0001t0001g0244others(6): 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 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0184a0001c0002t0001g0020a0001c0002t0001g0021others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0214 | 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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0145 | 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 | GAT | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 153 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.617+2337_617+2338i others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145634081 | ||||||
chr1:145634081
|
G | GTT | 108 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(105): 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 | a0001c0001t0001g0191a0001c0001t0001g0192 | 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 | a0001c0001t0001g0191a0001c0001t0001g0192 | 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 | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0033 | 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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0039others(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 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0216 | 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 | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | 7 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0105others(4): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | a0001c0001t0003g0098 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.617+4568A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145636312 | ||||||
chr1:145636334
|
A | AT | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.617+4597dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145636334 | |||||
chr1:145636644
|
C | G | 12 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0111 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0104 | 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 | 15 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(12): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0110a0001c0001t0001g0258a0001c0002t0001g0020others(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 | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0001g0110a0001c0002t0001g0020a0001c0002t0001g0021others(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 | a0001c0001t0001g0110a0001c0002t0001g0020a0001c0002t0001g0021others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0110 | 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 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0002t0001g0020others(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 | a0001c0002t0002g0141a0001c0002t0002g0142a0001c0002t0002g0143others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0012a0001c0001t0001g0154a0001c0001t0001g0199others(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 | a0001c0001t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-3756A>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640113 | ||||||
chr1:145640216
|
C | CA | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.618-3642dupA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145640216 | |||||
chr1:145640272
|
G | GA | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0110 | 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 | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.618-3177delA | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145640691 | ||||||
chr1:145640692
|
A | C | 2 | a0001c0001t0001g0077a0001c0002t0001g0145 | 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 | a0001c0001t0001g0077a0001c0002t0001g0145 | 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 | a0001c0001t0001g0077a0001c0002t0001g0145 | 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 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0040others(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 | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): 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 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0154others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110a0001c0002t0001g0145 | 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 | a0001c0001t0001g0110a0001c0002t0001g0020a0001c0002t0001g0021others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0110 | 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 | 7 | a0001c0001t0001g0013a0001c0001t0001g0244a0001c0001t0001g0245others(4): 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 | a0001c0001t0001g0110a0001c0002t0001g0020a0001c0002t0001g0021others(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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0081 | 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 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0116 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110a0001c0001t0001g0252a0001c0001t0001g0254others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.618-884G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | chr1 | 145642985 | ||||||
chr1:145643053
|
A | AT | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.618-808dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 145643053 | |||||
chr1:145643136
|
A | C | 1 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0081 | 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 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 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 | a0001c0001t0001g0110a0001c0002t0001g0020a0001c0002t0001g0021others(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 | a0001c0002t0002g0141a0001c0002t0002g0142a0001c0002t0002g0143others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0043a0001c0001t0001g0044 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0043a0001c0001t0001g0044 | 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 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0185 | 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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0224a0001c0001t0001g0228 | 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 | a0001c0001t0001g0110 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0082others(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 | a0001c0001t0001g0045a0001c0001t0001g0046 | 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 | a0001c0001t0001g0250 | 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 | a0001c0002t0005g0025 | 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 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0024 | 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 | 46 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(43): Show | 49 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(46): 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 | a0001c0001t0001g0010a0001c0001t0001g0095a0001c0001t0001g0111others(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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0121 | 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 | a0001c0002t0001g0022a0001c0002t0001g0026a0001c0002t0002g0141 | 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 | 119 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(116): 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 | 66 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(63): 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 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0027others(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 | a0001c0002t0001g0018a0001c0002t0001g0019 | 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 | a0001c0002t0001g0018a0001c0002t0001g0019 | 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 | a0001c0001t0001g0042a0001c0001t0001g0092a0001c0001t0001g0152others(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 | a0001c0001t0001g0046a0001c0001t0001g0190a0001c0001t0001g0213 | 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 | a0001c0001t0001g0147a0001c0001t0001g0174 | 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 | a0001c0001t0001g0013a0001c0001t0001g0081a0001c0001t0001g0151others(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 | a0001c0003t0001g0120 | 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 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0033others(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 | a0001c0001t0001g0091a0001c0001t0001g0103a0001c0001t0001g0161others(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 | a0001c0002t0001g0018a0001c0002t0001g0019 | 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 | a0001c0002t0001g0016a0001c0002t0001g0017 | 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 | a0001c0002t0001g0018a0001c0002t0001g0019 | 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 | a0001c0001t0001g0042a0001c0001t0001g0092a0001c0001t0001g0152others(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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | 42 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(39): Show | 45 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.909+562T>C | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145647829 | ||||||
chr1:145647831
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): 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 | 68 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(65): Show | 72 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(69): 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0010a0001c0001t0001g0095a0001c0001t0001g0111others(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 | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): 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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0019others(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 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0054others(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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0136a0001c0002t0001g0016a0001c0002t0001g0019 | 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 | a0001c0001t0001g0010a0001c0001t0001g0095a0001c0001t0001g0111others(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 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0033others(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 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0048others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0048a0001c0001t0001g0088 | 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 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0082others(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 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0054others(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 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0048others(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 | 50 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(47): 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 | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(33): 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(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 | 23 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0067others(20): 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 | a0001c0001t0001g0104a0001c0001t0001g0171a0001c0001t0001g0181others(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 | 65 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0031others(62): 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 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0086others(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 | a0001c0001t0001g0006a0001c0001t0001g0091a0001c0001t0001g0103others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0009a0001c0001t0001g0092a0001c0001t0001g0152others(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 | a0001c0001t0001g0014a0001c0001t0001g0092a0001c0001t0001g0150others(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 | a0001c0001t0001g0171a0001c0002t0002g0141a0001c0004t0001g0089 | 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 | a0001c0002t0002g0141 | 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 | a0001c0001t0001g0117 | 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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | CTT | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.909+1230_909+1231d others(4): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145648487 | |||||
chr1:145648487
|
C | CTTTT | 11 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0254a0002c0005t0001g0255 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0057others(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 | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.909+1529_909+1530i others(3): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648796 | ||||||
chr1:145648798
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.909+1531C>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648798 | ||||||
chr1:145648817
|
G | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.909+1550G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648817 | ||||||
chr1:145648818
|
T | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.909+1551T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145648818 | ||||||
chr1:145648825
|
C | T | 1 | a0001c0001t0001g0178 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0034a0001c0001t0001g0035 | 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 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0152a0001c0001t0001g0153 | 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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.909+2405G>T | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145649672 | ||||||
chr1:145649980
|
A | AT | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.909+2722dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145649980 | |||||
chr1:145650041
|
T | C | 1 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0168a0001c0001t0001g0218 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0224a0001c0001t0001g0228 | 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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0131 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0027a0001c0001t0001g0047 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0057 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0100 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0027a0001c0001t0001g0047 | 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 | a0001c0001t0001g0027a0001c0001t0001g0047 | 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 | a0001c0001t0001g0027a0001c0001t0001g0047 | 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 | a0001c0001t0001g0131 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0231 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0116 | 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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0232 | 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 | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 154 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(151): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0076a0001c0001t0001g0094 | 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 | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0130a0001c0001t0001g0132 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0010a0001c0001t0001g0148a0001c0001t0001g0150others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(2): 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 | a0001c0001t0001g0051 | 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 | 4 | a0001c0001t0001g0063a0001c0001t0001g0090a0001c0001t0001g0092others(1): Show | 4 | HG00423.hp1 HG00735.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+7150G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654417 | ||||||
chr1:145654451
|
G | T | 1 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0014a0001c0001t0001g0085a0001c0001t0001g0104others(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 | TCAA | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.909+7284_909+7285i others(5): Show |
GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654551 | ||||||
chr1:145654551
|
T | TCAAA | 18 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0039others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | ||||||
chr1:145654553
|
C | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.909+7286C>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145654553 | ||||||
chr1:145654572
|
C | A | 1 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0195 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0002g0141 | 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 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0115others(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 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0100 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0082 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0073 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0106 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 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 | 15 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0128others(12): 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 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0045others(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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | 37 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0073others(34): 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 | a0001c0002t0001g0023a0001c0002t0001g0024 | 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 | a0001c0001t0001g0168 | 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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0049 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0150a0001c0001t0001g0155a0001c0001t0001g0205others(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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0187 | 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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020 | 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 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0099 | 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 | a0001c0001t0001g0257 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0114 | 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 | a0001c0002t0001g0016a0001c0002t0001g0017 | 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 | a0001c0002t0001g0016a0001c0002t0001g0017 | 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 | a0001c0001t0001g0203a0001c0001t0001g0253 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0110 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0080 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0256 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03492.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.910-1139G>A | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | chr1 | 145662190 | ||||||
chr1:145662853
|
C | CT | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.910-470dupT | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 145662853 | |||||
chr1:145663165
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 135 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(132): 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0223others(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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0216 | 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 | 11 | a0001c0001t0001g0011a0001c0001t0001g0146a0001c0001t0001g0147others(8): 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0071 | 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 | a0001c0001t0001g0059a0001c0001t0001g0122 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0181 | 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 | a0001c0002t0001g0022 | 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 | a0001c0004t0001g0089 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0236a0001c0002t0001g0020a0001c0002t0001g0021others(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 | a0001c0002t0001g0145 | 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 | a0001c0001t0001g0247 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0002g0143 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(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 | a0001c0001t0001g0010a0001c0001t0001g0148a0001c0001t0001g0156others(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 | a0001c0001t0001g0078a0001c0002t0001g0145 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0043a0001c0001t0001g0044 | 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 | a0001c0001t0001g0231 | 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 | a0001c0002t0001g0145 | 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 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098 | 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 | a0001c0001t0001g0012 | 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 | 2 | a0001c0001t0001g0061a0001c0001t0001g0068 | 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 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(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 | a0001c0001t0001g0012 | 2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1161+28T>G | GPR89A | ENSG00000117262.19 | transcript | ENST00000313835.14 | protein_coding | 13/13 | chr1 | 145669718 |