geneid | 2782 |
---|---|
ensemblid | ENSG00000078369.19 |
hgncid | 4396 |
symbol | GNB1 |
name | G protein subunit beta 1 |
refseq_nuc | NM_002074.5 |
refseq_prot | NP_002065.1 |
ensembl_nuc | ENST00000378609.9 |
ensembl_prot | ENSP00000367872.3 |
mane_status | MANE Select |
chr | chr1 |
start | 1785286 |
end | 1891087 |
strand | - |
ver | v1.2 |
region | chr1:1785286-1891087 |
region5000 | chr1:1780286-1896087 |
regionname0 | GNB1_chr1_1785286_1891087 |
regionname5000 | GNB1_chr1_1780286_1896087 |
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 | 340 | 336 | 90 | 48 | 146 | 14 | 36 | 106 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
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 | 1023 | 330 | 86 | 47 | 145 | 14 | 36 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
c0002 | 0/0 | 1023 | 5 | 4 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
c0003 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
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 | 2141 | 305 | 71 | 45 | 137 | 14 | 36 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0002 | 0/0 | 2141 | 8 | 8 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0003 | 0/0 | 2140 | 5 | 5 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0004 | 0/0 | 2143 | 2 | 2 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0005 | 0/0 | 2141 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0006 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0007 | 0/0 | 2141 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0008 | 0/0 | 2141 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0009 | 0/0 | 2141 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0010 | 0/0 | 2141 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0011 | 0/0 | 2141 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0012 | 0/0 | 2141 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0013 | 0/0 | 2141 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0014 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0015 | 0/0 | 2141 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0016 | 0/0 | 2141 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0017 | 0/0 | 2141 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0018 | 0/0 | 2141 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0019 | 0/0 | 2141 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
t0020 | 0/0 | 2141 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
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 | 1023 | 330 | 86 | 47 | 145 | 14 | 36 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0002 | 0/0 | 1023 | 5 | 4 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0003 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3163 | 299 | 67 | 44 | 136 | 14 | 36 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0002 | 0/0 | 3163 | 8 | 8 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0003 | 0/0 | 3162 | 5 | 5 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0004 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0005 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0006 | 0/0 | 3166 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0007 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0008 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0009 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0010 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0011 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0012 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0013 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0014 | 0/0 | 3162 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0015 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0016 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0017 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0018 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0019 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0001t0020 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0002t0001 | 0/0 | 3163 | 5 | 4 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
a0001c0003t0001 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | copy fasta | chr1 | 1780286 | 1896087 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0006g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0008g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0010g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0011g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0013g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0014g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0015g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0016g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0017g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0018g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0019g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0001t0020g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | PUR | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01433 | hp2 | a0001 | c0001 | t0009 | g0040 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02027 | hp1 | a0001 | c0001 | t0016 | g0311 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02451 | hp2 | a0001 | c0001 | t0012 | g0120 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0322 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0196 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | STU | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | STU | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18974 | hp2 | a0001 | c0001 | t0014 | g0185 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0249 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18982 | hp2 | a0001 | c0001 | t0011 | g0178 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18994 | hp2 | a0001 | c0001 | t0017 | g0031 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | LWK | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19065 | hp1 | a0001 | c0001 | t0019 | g0332 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19067 | hp2 | a0001 | c0001 | t0015 | g0258 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19077 | hp1 | a0001 | c0001 | t0020 | g0333 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | YRI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG01123 | hp2 | a0001 | c0001 | t0018 | g0314 | AMR | CLM | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | MSL | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | USA | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | USA | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | USA | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0235 | REF | REF | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0179 | REF | REF | GNB1_chr1_1780286_1896087 | GNB1 | chr1 | 1780286 | 1896087 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:1793280
|
G | A | 1 | a0001c0002 | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
synonymous_variant | LOW | c.462C>T | p.Asp154Asp | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/12 | 825/3163 | 462/1023 | 154/340 | chr1 | 1793280 | ||
chr1:1804549
|
G | T | 1 | a0001c0003 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.300C>A | p.Val100Val | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/12 | 663/3163 | 300/1023 | 100/340 | chr1 | 1804549 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:1785579
|
G | A | 1 | a0001c0001t0013 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1484C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 1752 | chr1 | 1785579 | |||||
chr1:1785803
|
CT | C | 3 | a0001c0001t0003a0001c0001t0004a0001c0001t0014 | 8 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1259delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 1527 | chr1 | 1785803 | |||||
chr1:1785854
|
A | G | 1 | a0001c0001t0012 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1209T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 1477 | chr1 | 1785854 | |||||
chr1:1785908
|
G | A | 1 | a0001c0001t0010 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1155C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 1423 | chr1 | 1785908 | |||||
chr1:1786279
|
C | T | 1 | a0001c0001t0011 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*784G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 1052 | chr1 | 1786279 | |||||
chr1:1786297
|
T | C | 1 | a0001c0001t0015 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*766A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 1034 | chr1 | 1786297 | |||||
chr1:1786326
|
G | C | 1 | a0001c0001t0016 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*737C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 1005 | chr1 | 1786326 | |||||
chr1:1786409
|
G | T | 2 | a0001c0001t0002a0001c0001t0010 | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*654C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 922 | chr1 | 1786409 | |||||
chr1:1786460
|
C | T | 2 | a0001c0001t0003a0001c0001t0004 | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*603G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 871 | chr1 | 1786460 | |||||
chr1:1786691
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 640 | chr1 | 1786691 | |||||
chr1:1786692
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 639 | chr1 | 1786692 | |||||
chr1:1786694
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*369G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 637 | chr1 | 1786694 | |||||
chr1:1786696
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 635 | chr1 | 1786696 | |||||
chr1:1786697
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*366T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 634 | chr1 | 1786697 | |||||
chr1:1786698
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 633 | chr1 | 1786698 | |||||
chr1:1786702
|
C | A | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*361G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 629 | chr1 | 1786702 | |||||
chr1:1786703
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 628 | chr1 | 1786703 | |||||
chr1:1786704
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*359T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 627 | chr1 | 1786704 | |||||
chr1:1786705
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*358T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 626 | chr1 | 1786705 | |||||
chr1:1786708
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*355G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 623 | chr1 | 1786708 | |||||
chr1:1786710
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 621 | chr1 | 1786710 | |||||
chr1:1786712
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 619 | chr1 | 1786712 | |||||
chr1:1786713
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*350C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 618 | chr1 | 1786713 | |||||
chr1:1786715
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 616 | chr1 | 1786715 | |||||
chr1:1786716
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*347C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 615 | chr1 | 1786716 | |||||
chr1:1786717
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*346T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 614 | chr1 | 1786717 | |||||
chr1:1786718
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*345T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 613 | chr1 | 1786718 | |||||
chr1:1786719
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 612 | chr1 | 1786719 | |||||
chr1:1786721
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*342C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 610 | chr1 | 1786721 | |||||
chr1:1786723
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*340C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 608 | chr1 | 1786723 | |||||
chr1:1786725
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*338C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 606 | chr1 | 1786725 | |||||
chr1:1786727
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 604 | chr1 | 1786727 | |||||
chr1:1786729
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*334C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 602 | chr1 | 1786729 | |||||
chr1:1786731
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 600 | chr1 | 1786731 | |||||
chr1:1786735
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 596 | chr1 | 1786735 | |||||
chr1:1786736
|
A | G | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*327T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 595 | chr1 | 1786736 | |||||
chr1:1786737
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 594 | chr1 | 1786737 | |||||
chr1:1786740
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*323T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 591 | chr1 | 1786740 | |||||
chr1:1786741
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 590 | chr1 | 1786741 | |||||
chr1:1786742
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 589 | chr1 | 1786742 | |||||
chr1:1786743
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*320G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 588 | chr1 | 1786743 | |||||
chr1:1786745
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 586 | chr1 | 1786745 | |||||
chr1:1786747
|
A | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 584 | chr1 | 1786747 | |||||
chr1:1786749
|
T | C | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*314A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 582 | chr1 | 1786749 | |||||
chr1:1786752
|
A | G | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 579 | chr1 | 1786752 | |||||
chr1:1786753
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*310G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 578 | chr1 | 1786753 | |||||
chr1:1786754
|
C | G | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 577 | chr1 | 1786754 | |||||
chr1:1786756
|
T | G | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 575 | chr1 | 1786756 | |||||
chr1:1786757
|
C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*306G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 574 | chr1 | 1786757 | |||||
chr1:1786760
|
G | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 571 | chr1 | 1786760 | |||||
chr1:1786762
|
T | G | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 569 | chr1 | 1786762 | |||||
chr1:1786765
|
C | G | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*298G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 566 | chr1 | 1786765 | |||||
chr1:1786767
|
T | G | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 564 | chr1 | 1786767 | |||||
chr1:1786768
|
T | A | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 563 | chr1 | 1786768 | |||||
chr1:1786832
|
G | A | 1 | a0001c0001t0018 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*231C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 499 | chr1 | 1786832 | |||||
chr1:1786996
|
C | G | 1 | a0001c0001t0009 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 12/12 | 335 | chr1 | 1786996 | |||||
chr1:1890894
|
G | T | 1 | a0001c0001t0008 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-170C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65441 | chr1 | 1890894 | |||||
chr1:1890900
|
C | A | 1 | a0001c0001t0019 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-176G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65447 | chr1 | 1890900 | |||||
chr1:1890952
|
A | C | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-228T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65499 | chr1 | 1890952 | |||||
chr1:1890954
|
T | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-230A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65501 | chr1 | 1890954 | |||||
chr1:1890955
|
C | T | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-231G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65502 | chr1 | 1890955 | |||||
chr1:1890956
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-232G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65503 | chr1 | 1890956 | |||||
chr1:1890957
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-233G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65504 | chr1 | 1890957 | |||||
chr1:1890958
|
G | C | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-234C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65505 | chr1 | 1890958 | |||||
chr1:1890959
|
C | T | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-235G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65506 | chr1 | 1890959 | |||||
chr1:1890960
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-236G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65507 | chr1 | 1890960 | |||||
chr1:1890962
|
C | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-238G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65509 | chr1 | 1890962 | |||||
chr1:1890967
|
G | T | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-243C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65514 | chr1 | 1890967 | |||||
chr1:1890971
|
C | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-247G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65518 | chr1 | 1890971 | |||||
chr1:1890972
|
T | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-248A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65519 | chr1 | 1890972 | |||||
chr1:1890973
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-249G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65520 | chr1 | 1890973 | |||||
chr1:1890974
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-250G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65521 | chr1 | 1890974 | |||||
chr1:1890975
|
A | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-251T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65522 | chr1 | 1890975 | |||||
chr1:1890977
|
T | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-253A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65524 | chr1 | 1890977 | |||||
chr1:1890978
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-254G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65525 | chr1 | 1890978 | |||||
chr1:1890979
|
C | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-255G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65526 | chr1 | 1890979 | |||||
chr1:1890983
|
C | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-259G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65530 | chr1 | 1890983 | |||||
chr1:1890984
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-260G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65531 | chr1 | 1890984 | |||||
chr1:1890985
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-261G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65532 | chr1 | 1890985 | |||||
chr1:1890996
|
T | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-272A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65543 | chr1 | 1890996 | |||||
chr1:1890999
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-275G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65546 | chr1 | 1890999 | |||||
chr1:1891002
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-278G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65549 | chr1 | 1891002 | |||||
chr1:1891004
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-280G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65551 | chr1 | 1891004 | |||||
chr1:1891007
|
T | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-283A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65554 | chr1 | 1891007 | |||||
chr1:1891008
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-284G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65555 | chr1 | 1891008 | |||||
chr1:1891010
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-286G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65557 | chr1 | 1891010 | |||||
chr1:1891010
|
C | T | 1 | a0001c0001t0007 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-286G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65557 | chr1 | 1891010 | |||||
chr1:1891012
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-288G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65559 | chr1 | 1891012 | |||||
chr1:1891013
|
T | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-289A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65560 | chr1 | 1891013 | |||||
chr1:1891014
|
C | CCCG | 2 | a0001c0001t0004a0001c0001t0006 | 3 | HG02129.hp2 HG02895.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-293_-291dupCGG | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65562 | chr1 | 1891014 | |||||
chr1:1891014
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-290G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65561 | chr1 | 1891014 | |||||
chr1:1891016
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-292G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65563 | chr1 | 1891016 | |||||
chr1:1891018
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-294G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65565 | chr1 | 1891018 | |||||
chr1:1891019
|
C | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-295G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | chr1 | 1891019 | ||||||
chr1:1891022
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-298G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65569 | chr1 | 1891022 | |||||
chr1:1891024
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-300G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65571 | chr1 | 1891024 | |||||
chr1:1891027
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-303G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65574 | chr1 | 1891027 | |||||
chr1:1891030
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-306G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65577 | chr1 | 1891030 | |||||
chr1:1891033
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-309G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65580 | chr1 | 1891033 | |||||
chr1:1891034
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-310G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65581 | chr1 | 1891034 | |||||
chr1:1891035
|
T | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-311A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65582 | chr1 | 1891035 | |||||
chr1:1891039
|
T | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-315A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65586 | chr1 | 1891039 | |||||
chr1:1891040
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-316G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65587 | chr1 | 1891040 | |||||
chr1:1891041
|
C | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-317G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | chr1 | 1891041 | ||||||
chr1:1891043
|
C | T | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-319G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65590 | chr1 | 1891043 | |||||
chr1:1891044
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-320G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65591 | chr1 | 1891044 | |||||
chr1:1891045
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-321G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65592 | chr1 | 1891045 | |||||
chr1:1891046
|
C | A | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-322G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | chr1 | 1891046 | ||||||
chr1:1891047
|
T | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-323A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65594 | chr1 | 1891047 | |||||
chr1:1891051
|
A | C | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-327T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65598 | chr1 | 1891051 | |||||
chr1:1891056
|
T | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-332A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65603 | chr1 | 1891056 | |||||
chr1:1891058
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-334G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65605 | chr1 | 1891058 | |||||
chr1:1891059
|
A | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-335T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65606 | chr1 | 1891059 | |||||
chr1:1891060
|
G | C | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-336C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65607 | chr1 | 1891060 | |||||
chr1:1891061
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-337G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65608 | chr1 | 1891061 | |||||
chr1:1891062
|
C | G | 1 | a0001c0001t0005 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-338G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65609 | chr1 | 1891062 | |||||
chr1:1891067
|
G | A | 1 | a0001c0001t0020 | 1 | NA19077.hp1 | 5_prime_UTR_variant | MODIFIER | c.-343C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/12 | 65614 | chr1 | 1891067 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:1787079
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*10-26A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 11/11 | chr1 | 1787079 | ||||||
chr1:1787203
|
C | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01934.hp2 HG02300.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.*9+119G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 11/11 | chr1 | 1787203 | ||||||
chr1:1787572
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.917-135C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1787572 | ||||||
chr1:1787640
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.917-203C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1787640 | ||||||
chr1:1787755
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.917-318C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1787755 | ||||||
chr1:1788015
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0163 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.917-578G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788015 | ||||||
chr1:1788028
|
C | CA | 13 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0054others(10): Show | 13 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.917-592dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788028 | ||||||
chr1:1788028
|
CA | C | 9 | a0001c0001t0001g0186a0001c0001t0001g0263a0001c0001t0003g0290others(6): Show | 9 | HG02109.hp1 HG02602.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.917-592delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788028 | ||||||
chr1:1788551
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0104others(1): Show | 4 | NA18980.hp1 NA18994.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.916+502G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788551 | ||||||
chr1:1788683
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0181 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.916+370C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788683 | ||||||
chr1:1788773
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.916+280G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788773 | ||||||
chr1:1788782
|
G | C | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.916+271C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788782 | ||||||
chr1:1788842
|
G | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.916+211C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788842 | ||||||
chr1:1788918
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0013g0196 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.916+135C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788918 | ||||||
chr1:1788997
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.916+56A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1788997 | ||||||
chr1:1789048
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.916+5G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 10/11 | chr1 | 1789048 | ||||||
chr1:1789558
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-289C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789558 | ||||||
chr1:1789564
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.700-295G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789564 | ||||||
chr1:1789605
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-336G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789605 | ||||||
chr1:1789624
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.700-355C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789624 | ||||||
chr1:1789695
|
CA | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.700-427delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789695 | ||||||
chr1:1789711
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0013g0196 | 2 | HG02293.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.700-442T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789711 | ||||||
chr1:1789714
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.700-445C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789714 | ||||||
chr1:1789715
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.700-446A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789715 | ||||||
chr1:1789842
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.699+553A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789842 | ||||||
chr1:1789930
|
G | A | 1 | a0001c0001t0007g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.699+465C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1789930 | ||||||
chr1:1790040
|
C | T | 100 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.699+355G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1790040 | ||||||
chr1:1790042
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.699+353G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1790042 | ||||||
chr1:1790074
|
G | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.699+321C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1790074 | ||||||
chr1:1790110
|
G | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG03225.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.699+285C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1790110 | ||||||
chr1:1790234
|
AGAAGTTT others(7): Show |
A | 1 | a0001c0001t0001g0114 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.699+147_699+160del others(14): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1790234 | ||||||
chr1:1790368
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.699+27G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 9/11 | chr1 | 1790368 | ||||||
chr1:1790609
|
C | T | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-13G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1790609 | ||||||
chr1:1790627
|
C | G | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.498-31G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1790627 | ||||||
chr1:1790895
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.498-299G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1790895 | ||||||
chr1:1790976
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.498-380C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1790976 | ||||||
chr1:1791146
|
C | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0210a0001c0003t0001g0249 | 3 | HG00609.hp1 NA18980.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.498-550G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791146 | ||||||
chr1:1791172
|
A | AT | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.498-577dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791172 | ||||||
chr1:1791172
|
A | ATT | 13 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0077others(10): Show | 13 | HG01175.hp1 HG01433.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-578_498-577dup others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791172 | ||||||
chr1:1791172
|
A | ATTT | 7 | a0001c0001t0001g0161a0001c0001t0003g0290a0001c0001t0003g0291others(4): Show | 7 | HG01099.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-579_498-577dup others(3): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791172 | ||||||
chr1:1791246
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.498-650T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791246 | ||||||
chr1:1791389
|
G | A | 59 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.498-793C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791389 | ||||||
chr1:1791394
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0197 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.498-798G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791394 | ||||||
chr1:1791417
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.498-821G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791417 | ||||||
chr1:1791445
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.498-849C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791445 | ||||||
chr1:1791493
|
C | T | 100 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.498-897G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791493 | ||||||
chr1:1791592
|
G | A | 100 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.498-996C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791592 | ||||||
chr1:1791825
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-1229T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1791825 | ||||||
chr1:1792009
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.497+1236G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792009 | ||||||
chr1:1792166
|
T | C | 1 | a0001c0002t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.497+1079A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792166 | ||||||
chr1:1792189
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.497+1056C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792189 | ||||||
chr1:1792229
|
T | C | 1 | a0001c0001t0007g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.497+1016A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792229 | ||||||
chr1:1792462
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0055others(1): Show | 4 | NA18961.hp1 NA18962.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+783G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792462 | ||||||
chr1:1792466
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0134 | 3 | HG03491.hp2 HG03492.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.497+779G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792466 | ||||||
chr1:1792578
|
T | A | 1 | a0001c0003t0001g0249 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.497+667A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792578 | ||||||
chr1:1792647
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0329 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.497+598C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792647 | ||||||
chr1:1792696
|
C | CA | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(141): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.497+548dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792696 | ||||||
chr1:1792696
|
C | CAA | 8 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0058others(5): Show | 8 | HG00609.hp2 HG02074.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.497+547_497+548dup others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792696 | ||||||
chr1:1792696
|
CAA | C | 12 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+547_497+548del others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792696 | ||||||
chr1:1792707
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497+538T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792707 | ||||||
chr1:1792715
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.497+530T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792715 | ||||||
chr1:1792841
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.497+404T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792841 | ||||||
chr1:1792843
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.497+402C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792843 | ||||||
chr1:1792927
|
G | A | 100 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.497+318C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1792927 | ||||||
chr1:1793064
|
C | CA | 93 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.497+180dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1793064 | ||||||
chr1:1793172
|
T | C | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.497+73A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 8/11 | chr1 | 1793172 | ||||||
chr1:1793401
|
G | A | 1 | a0001c0001t0003g0291 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431-90C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1793401 | ||||||
chr1:1793577
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0138others(6): Show | 9 | NA18943.hp2 NA18962.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-266C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1793577 | ||||||
chr1:1793637
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-326C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1793637 | ||||||
chr1:1793822
|
A | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.431-511T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1793822 | ||||||
chr1:1793969
|
G | A | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-658C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1793969 | ||||||
chr1:1794130
|
C | T | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.431-819G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794130 | ||||||
chr1:1794156
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.431-845G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794156 | ||||||
chr1:1794187
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(54): Show | 59 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.431-876G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794187 | ||||||
chr1:1794258
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.431-947C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794258 | ||||||
chr1:1794321
|
C | T | 77 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.431-1010G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794321 | ||||||
chr1:1794398
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.431-1087C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794398 | ||||||
chr1:1794411
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.431-1100A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794411 | ||||||
chr1:1794433
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-1122C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794433 | ||||||
chr1:1794444
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-1133T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794444 | ||||||
chr1:1794750
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.431-1439T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794750 | ||||||
chr1:1794751
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.431-1440A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794751 | ||||||
chr1:1794767
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.431-1456G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794767 | ||||||
chr1:1794967
|
C | A | 3 | a0001c0001t0001g0230a0001c0001t0001g0259a0001c0001t0001g0264 | 3 | HG00558.hp2 HG02080.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.431-1656G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1794967 | ||||||
chr1:1795012
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.431-1701C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795012 | ||||||
chr1:1795061
|
T | G | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.431-1750A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795061 | ||||||
chr1:1795067
|
C | A | 1 | a0001c0001t0001g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.431-1756G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795067 | ||||||
chr1:1795095
|
G | A | 1 | a0001c0001t0003g0291 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431-1784C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795095 | ||||||
chr1:1795214
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0318 | 2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.431-1903C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795214 | ||||||
chr1:1795234
|
C | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-1923G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795234 | ||||||
chr1:1795388
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-2077T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795388 | ||||||
chr1:1795413
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.431-2102G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795413 | ||||||
chr1:1795493
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02572.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-2182G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795493 | ||||||
chr1:1795613
|
T | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(9): Show | 12 | HG01258.hp2 HG02293.hp1 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.431-2302A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795613 | ||||||
chr1:1795751
|
T | TCAAAAAA others(1): Show |
263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.431-2448_431-2441d others(10): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795751 | ||||||
chr1:1795781
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.431-2470A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795781 | ||||||
chr1:1795952
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-2641C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795952 | ||||||
chr1:1795960
|
G | A | 1 | a0001c0002t0001g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.431-2649C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1795960 | ||||||
chr1:1796074
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-2763C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1796074 | ||||||
chr1:1796151
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.431-2840T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1796151 | ||||||
chr1:1796207
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0013g0196 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.431-2896C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1796207 | ||||||
chr1:1796250
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.431-2939T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1796250 | ||||||
chr1:1796562
|
T | C | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02615.hp2 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.431-3251A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1796562 | ||||||
chr1:1797161
|
T | C | 1 | a0001c0001t0015g0258 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.431-3850A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797161 | ||||||
chr1:1797215
|
A | C | 1 | a0001c0001t0018g0314 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.431-3904T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797215 | ||||||
chr1:1797248
|
C | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.431-3937G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797248 | ||||||
chr1:1797299
|
G | C | 5 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01192.hp2 HG02647.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-3988C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797299 | ||||||
chr1:1797367
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.431-4056T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797367 | ||||||
chr1:1797456
|
T | G | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.431-4145A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797456 | ||||||
chr1:1797530
|
C | A | 97 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.431-4219G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797530 | ||||||
chr1:1797551
|
C | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-4240G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797551 | ||||||
chr1:1797569
|
C | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0160 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.431-4258G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797569 | ||||||
chr1:1797575
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0008g0009 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.431-4264G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797575 | ||||||
chr1:1797611
|
T | C | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.431-4300A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797611 | ||||||
chr1:1797783
|
C | T | 5 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-4472G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797783 | ||||||
chr1:1797876
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.431-4565C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1797876 | ||||||
chr1:1798387
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431-5076A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798387 | ||||||
chr1:1798460
|
C | T | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-5149G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798460 | ||||||
chr1:1798545
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-5234A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798545 | ||||||
chr1:1798733
|
G | A | 6 | a0001c0001t0001g0201a0001c0002t0001g0287a0001c0002t0001g0288others(3): Show | 6 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-5422C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798733 | ||||||
chr1:1798786
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.431-5475A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798786 | ||||||
chr1:1798827
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.431-5516C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798827 | ||||||
chr1:1798925
|
C | CT | 66 | a0001c0001t0001g0039a0001c0001t0001g0118a0001c0001t0001g0119others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.430+5493dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798925 | ||||||
chr1:1798925
|
C | CTT | 44 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0191others(41): Show | 44 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+5492_430+5493d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798925 | ||||||
chr1:1798954
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.430+5465G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798954 | ||||||
chr1:1798971
|
G | A | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+5448C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798971 | ||||||
chr1:1798974
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(54): Show | 59 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.430+5445G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1798974 | ||||||
chr1:1799076
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.430+5343A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1799076 | ||||||
chr1:1799133
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.430+5286C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1799133 | ||||||
chr1:1799218
|
C | A | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+5201G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1799218 | ||||||
chr1:1799675
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+4744C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1799675 | ||||||
chr1:1799799
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0013g0196 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.430+4620T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1799799 | ||||||
chr1:1800029
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.430+4390A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800029 | ||||||
chr1:1800082
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0166 | 3 | HG02145.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.430+4337G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800082 | ||||||
chr1:1800201
|
C | T | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430+4218G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800201 | ||||||
chr1:1800752
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+3667A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800752 | ||||||
chr1:1800753
|
T | TA | 13 | a0001c0001t0001g0053a0001c0001t0001g0140a0001c0001t0001g0252others(10): Show | 13 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+3665dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800753 | ||||||
chr1:1800753
|
TA | T | 16 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0069others(13): Show | 16 | HG00733.hp2 HG01243.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.430+3665delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800753 | ||||||
chr1:1800754
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.430+3665T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800754 | ||||||
chr1:1800768
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.430+3651T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800768 | ||||||
chr1:1800942
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+3477G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800942 | ||||||
chr1:1800963
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.430+3456G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1800963 | ||||||
chr1:1801096
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.430+3323A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1801096 | ||||||
chr1:1801188
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0068others(80): Show | 85 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.430+3231A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1801188 | ||||||
chr1:1801380
|
G | C | 1 | a0001c0001t0018g0314 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.430+3039C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1801380 | ||||||
chr1:1801552
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+2867A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1801552 | ||||||
chr1:1801625
|
A | C | 1 | a0001c0002t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.430+2794T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1801625 | ||||||
chr1:1801780
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0021others(169): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.430+2639T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1801780 | ||||||
chr1:1802238
|
A | G | 1 | a0001c0001t0001g0310 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.430+2181T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802238 | ||||||
chr1:1802404
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0156others(1): Show | 5 | NA18964.hp2 NA18974.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+2015T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802404 | ||||||
chr1:1802419
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.430+2000T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802419 | ||||||
chr1:1802521
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0190others(1): Show | 4 | HG01192.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1898G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802521 | ||||||
chr1:1802763
|
T | TA | 7 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0117others(4): Show | 7 | HG00738.hp1 HG02451.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+1655dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802763 | ||||||
chr1:1802763
|
T | TAA | 81 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.430+1654_430+1655d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802763 | ||||||
chr1:1802763
|
T | TAAA | 13 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0050others(10): Show | 13 | HG02145.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+1653_430+1655d others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802763 | ||||||
chr1:1802801
|
G | A | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430+1618C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802801 | ||||||
chr1:1802898
|
T | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(18): Show | 21 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+1521A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802898 | ||||||
chr1:1802929
|
T | A | 1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.430+1490A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1802929 | ||||||
chr1:1803041
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.430+1378G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803041 | ||||||
chr1:1803093
|
T | C | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.430+1326A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803093 | ||||||
chr1:1803119
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.430+1300A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803119 | ||||||
chr1:1803205
|
A | G | 4 | a0001c0001t0001g0130a0001c0001t0001g0208a0001c0001t0001g0250others(1): Show | 4 | HG02056.hp1 NA18947.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+1214T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803205 | ||||||
chr1:1803408
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+1011A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803408 | ||||||
chr1:1803441
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.430+978C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803441 | ||||||
chr1:1803531
|
C | T | 89 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.430+888G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803531 | ||||||
chr1:1803537
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.430+882G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803537 | ||||||
chr1:1803557
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0013g0196 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.430+862G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803557 | ||||||
chr1:1803664
|
G | A | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.430+755C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803664 | ||||||
chr1:1803827
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.430+592G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803827 | ||||||
chr1:1803843
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0064others(1): Show | 4 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+576C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803843 | ||||||
chr1:1803850
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0265 | 2 | HG02165.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.430+569G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803850 | ||||||
chr1:1803851
|
G | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0166 | 3 | HG02145.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.430+568C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803851 | ||||||
chr1:1803896
|
C | T | 1 | a0001c0001t0013g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.430+523G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803896 | ||||||
chr1:1803979
|
CT | C | 4 | a0001c0001t0003g0290a0001c0001t0003g0292a0001c0001t0003g0293others(1): Show | 4 | HG02109.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+439delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803979 | ||||||
chr1:1803982
|
T | A | 2 | a0001c0001t0003g0291a0001c0001t0003g0294 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.430+437A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803982 | ||||||
chr1:1803982
|
T | TA | 13 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0058others(10): Show | 13 | HG02055.hp2 HG02056.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+436dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803982 | ||||||
chr1:1803992
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.430+427T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803992 | ||||||
chr1:1803999
|
AAAAAG | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0068others(3): Show | 6 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+415_430+419del others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1803999 | ||||||
chr1:1804002
|
AAG | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0088others(127): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+415_430+416del others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1804002 | ||||||
chr1:1804003
|
AG | A | 113 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.430+415delC | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1804003 | ||||||
chr1:1804004
|
G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0016others(71): Show | 75 | HG00544.hp1 HG00673.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.430+415C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1804004 | ||||||
chr1:1804214
|
G | A | 1 | a0001c0001t0013g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.430+205C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1804214 | ||||||
chr1:1804231
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.430+188C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1804231 | ||||||
chr1:1804368
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.430+51G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 7/11 | chr1 | 1804368 | ||||||
chr1:1804836
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.268-255C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1804836 | ||||||
chr1:1805086
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0104others(1): Show | 4 | NA18980.hp1 NA18994.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-505G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805086 | ||||||
chr1:1805087
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.268-506C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805087 | ||||||
chr1:1805214
|
T | G | 79 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.268-633A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805214 | ||||||
chr1:1805416
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.268-835T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805416 | ||||||
chr1:1805517
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.268-936T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805517 | ||||||
chr1:1805570
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0330 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.267+905G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805570 | ||||||
chr1:1805713
|
T | G | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+762A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805713 | ||||||
chr1:1805830
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.267+645G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805830 | ||||||
chr1:1805880
|
T | A | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+595A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1805880 | ||||||
chr1:1806009
|
C | A | 1 | a0001c0001t0001g0271 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.267+466G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1806009 | ||||||
chr1:1806103
|
A | T | 6 | a0001c0001t0002g0308a0001c0001t0002g0323a0001c0001t0002g0324others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.267+372T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1806103 | ||||||
chr1:1806255
|
C | T | 1 | a0001c0001t0002g0327 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.267+220G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1806255 | ||||||
chr1:1806435
|
T | C | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.267+40A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1806435 | ||||||
chr1:1806456
|
G | A | 7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0204others(4): Show | 7 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+19C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1806456 | ||||||
chr1:1806461
|
C | T | 14 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0204others(11): Show | 14 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.267+14G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 6/11 | chr1 | 1806461 | ||||||
chr1:1806745
|
G | A | 1 | a0001c0002t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.204-207C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1806745 | ||||||
chr1:1806830
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0015g0258 | 2 | NA18906.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.204-292G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1806830 | ||||||
chr1:1806932
|
C | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0041others(5): Show | 8 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.204-394G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1806932 | ||||||
chr1:1807231
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0190others(1): Show | 4 | HG01192.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-693C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807231 | ||||||
chr1:1807289
|
C | T | 5 | a0001c0001t0001g0146a0001c0001t0001g0158a0001c0001t0001g0160others(2): Show | 5 | HG01099.hp1 HG02257.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-751G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807289 | ||||||
chr1:1807301
|
A | G | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-763T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807301 | ||||||
chr1:1807451
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.204-913C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807451 | ||||||
chr1:1807462
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0087 | 2 | HG03942.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.204-924A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807462 | ||||||
chr1:1807463
|
G | GA | 92 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0016others(89): Show | 92 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.204-926dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
G | GAA | 17 | a0001c0001t0001g0073a0001c0001t0001g0149a0001c0001t0001g0150others(14): Show | 17 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.204-927_204-926dup others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
G | GAAA | 9 | a0001c0001t0001g0119a0001c0001t0001g0154a0001c0001t0001g0252others(6): Show | 9 | HG01123.hp2 HG01192.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.204-928_204-926dup others(3): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
G | GAAAAAAA others(3): Show |
1 | a0001c0002t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.204-935_204-926dup others(10): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
G | GAAAAAAA others(18): Show |
1 | a0001c0001t0007g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.204-950_204-926dup others(25): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
G | GAAAAAAA others(21): Show |
1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.204-953_204-926dup others(28): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
GA | G | 22 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0020others(19): Show | 22 | HG00408.hp1 HG00733.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.204-926delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
GAAAAAAA others(1): Show |
G | 9 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG00642.hp2 HG04115.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.204-933_204-926del others(8): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
GAAAAAAA others(2): Show |
G | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(38): Show | 43 | HG00558.hp1 HG00733.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.204-934_204-926del others(9): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0096a0001c0001t0001g0213 | 2 | HG02155.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.204-935_204-926del others(10): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
GAAAAAAA others(4): Show |
G | 3 | a0001c0001t0001g0018a0001c0001t0001g0269a0001c0001t0013g0196 | 3 | HG00673.hp2 HG02895.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.204-936_204-926del others(11): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807463
|
GAAAAAAA others(5): Show |
G | 1 | a0001c0001t0001g0022 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.204-937_204-926del others(12): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807463 | ||||||
chr1:1807464
|
A | G | 1 | a0001c0001t0015g0258 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.204-926T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807464 | ||||||
chr1:1807466
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.204-928T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807466 | ||||||
chr1:1807494
|
C | A | 1 | a0001c0001t0002g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.204-956G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807494 | ||||||
chr1:1807545
|
C | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | NA18943.hp1 NA18994.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-1007G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807545 | ||||||
chr1:1807627
|
C | T | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.204-1089G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807627 | ||||||
chr1:1807832
|
C | T | 6 | a0001c0001t0001g0189a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.204-1294G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807832 | ||||||
chr1:1807989
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.204-1451C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1807989 | ||||||
chr1:1808004
|
C | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(14): Show | 17 | HG00423.hp2 HG00673.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.204-1466G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808004 | ||||||
chr1:1808384
|
AC | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0041others(4): Show | 7 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.204-1847delG | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808384 | ||||||
chr1:1808498
|
C | G | 1 | a0001c0001t0008g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.204-1960G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808498 | ||||||
chr1:1808563
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.204-2025G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808563 | ||||||
chr1:1808608
|
T | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.204-2070A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808608 | ||||||
chr1:1808642
|
TTTTG | T | 77 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.204-2108_204-2105d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808642 | ||||||
chr1:1808816
|
G | T | 100 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.204-2278C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808816 | ||||||
chr1:1808891
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.204-2353T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808891 | ||||||
chr1:1808964
|
A | G | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.204-2426T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1808964 | ||||||
chr1:1809072
|
A | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0279 | 2 | NA18944.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.204-2534T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809072 | ||||||
chr1:1809189
|
AT | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.204-2652delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809189 | ||||||
chr1:1809189
|
ATT | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0113others(6): Show | 9 | HG01516.hp2 HG02523.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.204-2653_204-2652d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809189 | ||||||
chr1:1809288
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.204-2750G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809288 | ||||||
chr1:1809537
|
C | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.204-2999G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809537 | ||||||
chr1:1809588
|
C | T | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02615.hp2 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.204-3050G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809588 | ||||||
chr1:1809707
|
AAGCTGTC others(20): Show |
A | 1 | a0001c0001t0001g0054 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.204-3196_204-3170d others(29): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809707 | ||||||
chr1:1809715
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-3177G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809715 | ||||||
chr1:1809759
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0045 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.204-3221C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809759 | ||||||
chr1:1809991
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.204-3453C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1809991 | ||||||
chr1:1810077
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(191): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.204-3539A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810077 | ||||||
chr1:1810079
|
T | A | 6 | a0001c0001t0001g0136a0001c0001t0001g0248a0001c0001t0001g0255others(3): Show | 6 | HG01243.hp2 HG02735.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.204-3541A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810079 | ||||||
chr1:1810086
|
A | G | 37 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.204-3548T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810086 | ||||||
chr1:1810114
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.204-3576A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810114 | ||||||
chr1:1810449
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0060others(4): Show | 7 | HG00423.hp2 HG02155.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.204-3911A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810449 | ||||||
chr1:1810535
|
CA | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.204-3998delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810535 | ||||||
chr1:1810535
|
CAA | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0127a0001c0001t0001g0136others(4): Show | 7 | HG02280.hp1 HG02523.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.204-3999_204-3998d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810535 | ||||||
chr1:1810535
|
CAAA | C | 9 | a0001c0001t0001g0197a0001c0001t0003g0290a0001c0001t0003g0291others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.204-4000_204-3998d others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810535 | ||||||
chr1:1810708
|
C | T | 1 | a0001c0001t0013g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.204-4170G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810708 | ||||||
chr1:1810882
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.204-4344C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810882 | ||||||
chr1:1810947
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0002t0001g0296 | 3 | HG02559.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.204-4409G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1810947 | ||||||
chr1:1811033
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.204-4495G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811033 | ||||||
chr1:1811050
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.204-4512A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811050 | ||||||
chr1:1811070
|
C | CAT | 18 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0042others(15): Show | 18 | HG01255.hp1 HG01258.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.204-4534_204-4533d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811070 | ||||||
chr1:1811079
|
A | AT | 4 | a0001c0001t0001g0146a0001c0001t0001g0161a0001c0001t0001g0284others(1): Show | 4 | HG01099.hp1 HG02615.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-4542dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811079 | ||||||
chr1:1811081
|
A | AT | 53 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(50): Show | 54 | HG00544.hp1 HG01123.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.204-4544dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811081 | ||||||
chr1:1811081
|
A | T | 6 | a0001c0001t0001g0146a0001c0001t0001g0161a0001c0001t0001g0183others(3): Show | 6 | HG01099.hp1 HG02615.hp2 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.204-4543T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811081 | ||||||
chr1:1811081
|
AT | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(48): Show | 53 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-4544delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811081 | ||||||
chr1:1811082
|
T | TA | 178 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.204-4545_204-4544i others(3): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811082 | ||||||
chr1:1811082
|
T | TATA | 3 | a0001c0001t0001g0127a0001c0001t0001g0202a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.204-4545_204-4544i others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811082 | ||||||
chr1:1811083
|
T | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0042others(15): Show | 18 | HG01258.hp2 HG01433.hp1 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.204-4545A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811083 | ||||||
chr1:1811084
|
T | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.204-4546A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811084 | ||||||
chr1:1811085
|
T | A | 7 | a0001c0001t0001g0117a0001c0001t0001g0203a0001c0001t0001g0224others(4): Show | 7 | HG01433.hp1 HG02602.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.204-4547A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811085 | ||||||
chr1:1811086
|
T | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0113others(17): Show | 21 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.204-4548A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811086 | ||||||
chr1:1811239
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01934.hp2 HG02300.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+4517G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811239 | ||||||
chr1:1811476
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.203+4280G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811476 | ||||||
chr1:1811536
|
G | GACA | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+4217_203+4219d others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811536 | ||||||
chr1:1811634
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.203+4122A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811634 | ||||||
chr1:1811761
|
C | T | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.203+3995G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811761 | ||||||
chr1:1811774
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+3982C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811774 | ||||||
chr1:1811885
|
G | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+3871C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1811885 | ||||||
chr1:1812011
|
A | G | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.203+3745T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812011 | ||||||
chr1:1812038
|
G | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.203+3718C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812038 | ||||||
chr1:1812065
|
C | CA | 10 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0058others(7): Show | 10 | HG02074.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.203+3690dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812065 | ||||||
chr1:1812068
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0003g0291 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.203+3687_203+3688i others(16): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812068 | ||||||
chr1:1812068
|
A | AAAAAAAA others(6): Show |
6 | a0001c0001t0003g0290a0001c0001t0003g0292a0001c0001t0003g0293others(3): Show | 6 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.203+3687_203+3688i others(15): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812068 | ||||||
chr1:1812077
|
C | A | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.203+3679G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812077 | ||||||
chr1:1812080
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.203+3676T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812080 | ||||||
chr1:1812203
|
T | TG | 7 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+3552dupC | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812203 | ||||||
chr1:1812239
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.203+3517G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812239 | ||||||
chr1:1812256
|
T | C | 1 | a0001c0001t0002g0327 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203+3500A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812256 | ||||||
chr1:1812393
|
TACACACA others(5): Show |
T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+3351_203+3362d others(14): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812393 | ||||||
chr1:1812407
|
T | TAC | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.203+3347_203+3348d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812407 | ||||||
chr1:1812407
|
T | TACAC | 6 | a0001c0001t0001g0139a0001c0001t0001g0255a0001c0001t0001g0277others(3): Show | 6 | HG01433.hp2 NA18951.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.203+3345_203+3348d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812407 | ||||||
chr1:1812419
|
C | T | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+3337G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812419 | ||||||
chr1:1812509
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.203+3247C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812509 | ||||||
chr1:1812698
|
C | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+3058G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812698 | ||||||
chr1:1812721
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.203+3035G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812721 | ||||||
chr1:1812962
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+2794A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1812962 | ||||||
chr1:1813304
|
C | T | 5 | a0001c0001t0001g0215a0001c0001t0001g0235a0001c0001t0001g0240others(2): Show | 5 | HG00280.hp1 HG00741.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+2452G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1813304 | ||||||
chr1:1813373
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.203+2383T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1813373 | ||||||
chr1:1813394
|
C | T | 8 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.203+2362G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1813394 | ||||||
chr1:1813451
|
A | G | 12 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0223others(9): Show | 12 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.203+2305T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1813451 | ||||||
chr1:1813618
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.203+2138C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1813618 | ||||||
chr1:1813634
|
G | C | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+2122C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1813634 | ||||||
chr1:1813745
|
C | T | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+2011G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1813745 | ||||||
chr1:1814279
|
C | T | 1 | a0001c0001t0007g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.203+1477G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814279 | ||||||
chr1:1814287
|
G | A | 42 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0191others(39): Show | 42 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.203+1469C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814287 | ||||||
chr1:1814408
|
AG | A | 5 | a0001c0001t0001g0238a0001c0001t0001g0248a0001c0001t0001g0256others(2): Show | 5 | HG02300.hp1 NA18612.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+1347delC | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814408 | ||||||
chr1:1814411
|
C | A | 5 | a0001c0001t0001g0238a0001c0001t0001g0248a0001c0001t0001g0256others(2): Show | 5 | HG02300.hp1 NA18612.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+1345G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814411 | ||||||
chr1:1814650
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.203+1106T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814650 | ||||||
chr1:1814677
|
C | T | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+1079G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814677 | ||||||
chr1:1814717
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.203+1039T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814717 | ||||||
chr1:1814797
|
C | CA | 77 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.203+958dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814797 | ||||||
chr1:1814797
|
C | CAA | 16 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0027others(13): Show | 16 | HG00639.hp1 HG01243.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.203+957_203+958dup others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814797 | ||||||
chr1:1814797
|
CAAAAAAA others(2): Show |
C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(53): Show | 58 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.203+950_203+958del others(9): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814797 | ||||||
chr1:1814814
|
A | G | 4 | a0001c0001t0001g0146a0001c0001t0001g0158a0001c0001t0001g0160others(1): Show | 4 | HG02257.hp1 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+942T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814814 | ||||||
chr1:1814815
|
A | AG | 96 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.203+940_203+941ins others(1): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814815 | ||||||
chr1:1814815
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.203+941T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814815 | ||||||
chr1:1814839
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.203+917C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814839 | ||||||
chr1:1814884
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.203+872C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814884 | ||||||
chr1:1814970
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+786T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814970 | ||||||
chr1:1814972
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+784A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1814972 | ||||||
chr1:1815004
|
A | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+752T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815004 | ||||||
chr1:1815011
|
G | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+745C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815011 | ||||||
chr1:1815036
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+720G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815036 | ||||||
chr1:1815037
|
G | A | 1 | a0001c0001t0011g0178 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.203+719C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815037 | ||||||
chr1:1815061
|
G | A | 5 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+695C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815061 | ||||||
chr1:1815065
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+691A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815065 | ||||||
chr1:1815094
|
A | G | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+662T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815094 | ||||||
chr1:1815112
|
TA | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0055a0001c0001t0001g0072others(7): Show | 10 | HG01081.hp1 HG01256.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.203+643delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815112 | ||||||
chr1:1815113
|
A | T | 6 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.203+643T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815113 | ||||||
chr1:1815114
|
A | T | 1 | a0001c0001t0004g0006 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.203+642T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815114 | ||||||
chr1:1815169
|
T | C | 5 | a0001c0001t0001g0146a0001c0001t0001g0158a0001c0001t0001g0160others(2): Show | 5 | HG01099.hp1 HG02257.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+587A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815169 | ||||||
chr1:1815255
|
G | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(47): Show | 52 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.203+501C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815255 | ||||||
chr1:1815264
|
G | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.203+492C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815264 | ||||||
chr1:1815360
|
C | A | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.203+396G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815360 | ||||||
chr1:1815620
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.203+136G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 5/11 | chr1 | 1815620 | ||||||
chr1:1815879
|
T | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0223others(5): Show | 8 | HG00408.hp2 HG00597.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-17A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1815879 | ||||||
chr1:1815937
|
G | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-75C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1815937 | ||||||
chr1:1815938
|
C | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-76G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1815938 | ||||||
chr1:1815985
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-123A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1815985 | ||||||
chr1:1816107
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.97-245A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816107 | ||||||
chr1:1816201
|
T | G | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-339A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816201 | ||||||
chr1:1816209
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.97-347G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816209 | ||||||
chr1:1816242
|
C | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-380G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816242 | ||||||
chr1:1816519
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.97-657G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816519 | ||||||
chr1:1816644
|
C | CT | 14 | a0001c0001t0001g0053a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.97-783dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816644 | ||||||
chr1:1816644
|
C | CTT | 6 | a0001c0001t0001g0149a0001c0001t0003g0290a0001c0001t0003g0292others(3): Show | 6 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-784_97-783dupAA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816644 | ||||||
chr1:1816644
|
CT | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(153): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.97-783delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816644 | ||||||
chr1:1816644
|
CTT | C | 9 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0134others(6): Show | 9 | HG01517.hp1 HG03491.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-784_97-783delAA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816644 | ||||||
chr1:1816760
|
T | C | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-898A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816760 | ||||||
chr1:1816809
|
T | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0111 | 2 | NA18973.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.97-947A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816809 | ||||||
chr1:1816827
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.97-965A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816827 | ||||||
chr1:1816922
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0231 | 2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.96+915C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1816922 | ||||||
chr1:1817037
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.96+800A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817037 | ||||||
chr1:1817169
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.96+668C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817169 | ||||||
chr1:1817186
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.96+651C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817186 | ||||||
chr1:1817213
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.96+624A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817213 | ||||||
chr1:1817277
|
C | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+560G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817277 | ||||||
chr1:1817295
|
T | C | 100 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.96+542A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817295 | ||||||
chr1:1817655
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+182A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817655 | ||||||
chr1:1817763
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+74G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817763 | ||||||
chr1:1817785
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.96+52C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 4/11 | chr1 | 1817785 | ||||||
chr1:1818095
|
C | A | 1 | a0001c0001t0003g0290 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-220G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818095 | ||||||
chr1:1818305
|
T | TA | 93 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0072others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.58-431dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818305 | ||||||
chr1:1818305
|
T | TAA | 6 | a0001c0001t0001g0128a0001c0001t0001g0193a0001c0001t0001g0209others(3): Show | 6 | HG01175.hp1 HG02738.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-432_58-431dupTT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818305 | ||||||
chr1:1818305
|
TA | T | 16 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0055others(13): Show | 16 | HG02280.hp2 HG02523.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.58-431delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818305 | ||||||
chr1:1818305
|
TAAAAAAA | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(53): Show | 58 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.58-437_58-431delTT others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818305 | ||||||
chr1:1818305
|
TAAAAAAA others(6): Show |
T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG03225.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.58-443_58-431delTT others(11): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818305 | ||||||
chr1:1818620
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0163 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58-745A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818620 | ||||||
chr1:1818661
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-786T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818661 | ||||||
chr1:1818663
|
G | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-788C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818663 | ||||||
chr1:1818691
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.58-816G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818691 | ||||||
chr1:1818741
|
T | C | 1 | a0001c0001t0001g0235 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.58-866A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818741 | ||||||
chr1:1818761
|
G | T | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-886C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1818761 | ||||||
chr1:1819253
|
T | C | 7 | a0001c0001t0001g0205a0001c0001t0001g0217a0001c0001t0001g0219others(4): Show | 7 | NA18942.hp1 NA18952.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-1378A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819253 | ||||||
chr1:1819254
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.58-1379G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819254 | ||||||
chr1:1819298
|
C | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0008g0009 | 3 | HG01243.hp1 HG01255.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-1423G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819298 | ||||||
chr1:1819335
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.58-1460C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819335 | ||||||
chr1:1819357
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-1482T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819357 | ||||||
chr1:1819370
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.58-1495C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819370 | ||||||
chr1:1819506
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.58-1631G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819506 | ||||||
chr1:1819522
|
C | CT | 6 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0086others(3): Show | 6 | HG02074.hp1 HG02109.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-1648dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819522 | ||||||
chr1:1819572
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0320 | 2 | HG00544.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.58-1697A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819572 | ||||||
chr1:1819610
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.58-1735G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819610 | ||||||
chr1:1819633
|
G | A | 1 | a0001c0001t0006g0005 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.58-1758C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819633 | ||||||
chr1:1819703
|
TA | T | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-1829delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819703 | ||||||
chr1:1819705
|
AT | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(216): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.58-1831delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819705 | ||||||
chr1:1819739
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.58-1864C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819739 | ||||||
chr1:1819825
|
G | A | 101 | a0001c0001t0001g0075a0001c0001t0001g0119a0001c0001t0001g0121others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.58-1950C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819825 | ||||||
chr1:1819828
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-1953A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1819828 | ||||||
chr1:1820114
|
C | T | 8 | a0001c0001t0001g0127a0001c0001t0003g0290a0001c0001t0003g0291others(5): Show | 8 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-2239G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820114 | ||||||
chr1:1820140
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0134 | 3 | HG03491.hp2 HG03492.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.58-2265A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820140 | ||||||
chr1:1820178
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.58-2303C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820178 | ||||||
chr1:1820247
|
T | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01256.hp1 HG01496.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.58-2372A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820247 | ||||||
chr1:1820249
|
T | C | 8 | a0001c0001t0001g0127a0001c0001t0003g0290a0001c0001t0003g0291others(5): Show | 8 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-2374A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820249 | ||||||
chr1:1820337
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(146): Show | 151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.58-2462T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820337 | ||||||
chr1:1820348
|
ACT | A | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-2475_58-2474del others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820348 | ||||||
chr1:1820356
|
T | TA | 36 | a0001c0001t0001g0058a0001c0001t0001g0119a0001c0001t0001g0121others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.58-2482dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820356 | ||||||
chr1:1820356
|
TA | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(128): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.58-2482delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820356 | ||||||
chr1:1820356
|
TAA | T | 8 | a0001c0001t0001g0055a0001c0001t0001g0072a0001c0001t0001g0080others(5): Show | 8 | HG00733.hp1 HG01256.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-2483_58-2482del others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820356 | ||||||
chr1:1820356
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0126 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.58-2493_58-2482del others(12): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820356 | ||||||
chr1:1820812
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.58-2937T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1820812 | ||||||
chr1:1821193
|
G | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.58-3318C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1821193 | ||||||
chr1:1821255
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02572.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-3380G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1821255 | ||||||
chr1:1821431
|
C | T | 1 | a0001c0001t0018g0314 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.58-3556G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1821431 | ||||||
chr1:1821516
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.58-3641G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1821516 | ||||||
chr1:1821518
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-3643A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1821518 | ||||||
chr1:1821700
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+3697G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1821700 | ||||||
chr1:1821701
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57+3696G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1821701 | ||||||
chr1:1821925
|
T | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.57+3472A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1821925 | ||||||
chr1:1822240
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.57+3157C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822240 | ||||||
chr1:1822242
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+3155T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822242 | ||||||
chr1:1822247
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(55): Show | 60 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.57+3150T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822247 | ||||||
chr1:1822300
|
C | CT | 8 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0057others(5): Show | 8 | HG01175.hp2 HG02074.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+3096dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822300 | ||||||
chr1:1822300
|
CT | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.57+3096delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822300 | ||||||
chr1:1822352
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+3045T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822352 | ||||||
chr1:1822447
|
C | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0080 | 3 | HG03540.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.57+2950G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822447 | ||||||
chr1:1822570
|
C | T | 12 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0223others(9): Show | 12 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+2827G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822570 | ||||||
chr1:1822606
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+2791G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822606 | ||||||
chr1:1822699
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.57+2698C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822699 | ||||||
chr1:1822747
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+2650T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822747 | ||||||
chr1:1822959
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+2438A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822959 | ||||||
chr1:1822987
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0070 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.57+2410T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822987 | ||||||
chr1:1822999
|
T | C | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+2398A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1822999 | ||||||
chr1:1823018
|
G | A | 9 | a0001c0001t0001g0197a0001c0001t0003g0290a0001c0001t0003g0291others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+2379C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1823018 | ||||||
chr1:1823242
|
G | GA | 57 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 57 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.57+2154dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1823242 | ||||||
chr1:1823242
|
GA | G | 15 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0097others(12): Show | 15 | HG00639.hp2 HG01496.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.57+2154delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1823242 | ||||||
chr1:1823242
|
GAAAAAAA others(4): Show |
G | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.57+2144_57+2154del others(11): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1823242 | ||||||
chr1:1823374
|
C | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+2023G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1823374 | ||||||
chr1:1823818
|
T | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+1579A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1823818 | ||||||
chr1:1823820
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+1577T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1823820 | ||||||
chr1:1823938
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+1459A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1823938 | ||||||
chr1:1824495
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.57+902C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1824495 | ||||||
chr1:1824496
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.57+901C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1824496 | ||||||
chr1:1824984
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.57+413C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1824984 | ||||||
chr1:1825020
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+377G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1825020 | ||||||
chr1:1825201
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0023 | 2 | HG01258.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.57+196A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 3/11 | chr1 | 1825201 | ||||||
chr1:1825697
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-46-198A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1825697 | ||||||
chr1:1825782
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0108a0001c0001t0001g0146others(44): Show | 48 | HG00544.hp1 HG00738.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.-46-283C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1825782 | ||||||
chr1:1825864
|
C | CA | 12 | a0001c0001t0001g0030a0001c0001t0001g0275a0001c0001t0001g0276others(9): Show | 12 | HG02145.hp1 HG02280.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46-366dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1825864 | ||||||
chr1:1825898
|
G | A | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0159others(5): Show | 8 | HG01192.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46-399C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1825898 | ||||||
chr1:1826011
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-46-512T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1826011 | ||||||
chr1:1826044
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-545A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1826044 | ||||||
chr1:1826129
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0330 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-46-630G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1826129 | ||||||
chr1:1826511
|
C | T | 1 | a0001c0003t0001g0249 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-46-1012G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1826511 | ||||||
chr1:1826627
|
G | C | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-46-1128C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1826627 | ||||||
chr1:1826921
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-46-1422C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1826921 | ||||||
chr1:1827114
|
T | A | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-1615A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827114 | ||||||
chr1:1827127
|
A | C | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-1628T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827127 | ||||||
chr1:1827150
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-46-1651G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827150 | ||||||
chr1:1827245
|
C | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-1746G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827245 | ||||||
chr1:1827381
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-1882A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827381 | ||||||
chr1:1827543
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0165 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-46-2044C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827543 | ||||||
chr1:1827587
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-46-2088A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827587 | ||||||
chr1:1827615
|
G | A | 66 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-46-2116C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827615 | ||||||
chr1:1827699
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-46-2200C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827699 | ||||||
chr1:1827703
|
C | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-2204G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827703 | ||||||
chr1:1827774
|
A | G | 100 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-46-2275T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827774 | ||||||
chr1:1827790
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-46-2291C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827790 | ||||||
chr1:1827913
|
A | C | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-2414T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1827913 | ||||||
chr1:1828038
|
C | T | 1 | a0001c0001t0009g0040 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-46-2539G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828038 | ||||||
chr1:1828041
|
C | T | 1 | a0001c0001t0020g0333 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-46-2542G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828041 | ||||||
chr1:1828042
|
T | G | 1 | a0001c0001t0020g0333 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-46-2543A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828042 | ||||||
chr1:1828045
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-46-2546C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828045 | ||||||
chr1:1828048
|
C | G | 1 | a0001c0001t0020g0333 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-46-2549G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828048 | ||||||
chr1:1828049
|
G | C | 1 | a0001c0001t0020g0333 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-46-2550C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828049 | ||||||
chr1:1828308
|
C | T | 22 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(19): Show | 22 | HG00558.hp1 HG02080.hp2 NA18747.hp1 others(19): Show |
intron_variant | MODIFIER | c.-46-2809G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828308 | ||||||
chr1:1828544
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-46-3045C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828544 | ||||||
chr1:1828545
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-46-3046G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828545 | ||||||
chr1:1828687
|
C | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0166 | 3 | HG02145.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-46-3188G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828687 | ||||||
chr1:1828833
|
G | A | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-46-3334C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828833 | ||||||
chr1:1828894
|
T | TAC | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-46-3397_-46-3396d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828894 | ||||||
chr1:1828979
|
A | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0165 | 2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-46-3480T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1828979 | ||||||
chr1:1829013
|
T | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0111a0001c0001t0001g0329 | 3 | HG03209.hp2 NA18973.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-46-3514A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829013 | ||||||
chr1:1829065
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-46-3566A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829065 | ||||||
chr1:1829129
|
T | C | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02615.hp2 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-46-3630A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829129 | ||||||
chr1:1829288
|
T | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0041others(4): Show | 7 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-3789A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829288 | ||||||
chr1:1829288
|
T | G | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-3789A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829288 | ||||||
chr1:1829352
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-46-3853C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829352 | ||||||
chr1:1829498
|
G | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0223others(5): Show | 8 | HG00408.hp2 HG00597.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46-3999C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829498 | ||||||
chr1:1829550
|
A | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-46-4051T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829550 | ||||||
chr1:1829654
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-46-4155C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829654 | ||||||
chr1:1829706
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-4207C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829706 | ||||||
chr1:1829727
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-46-4228C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829727 | ||||||
chr1:1829762
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-46-4263C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829762 | ||||||
chr1:1829897
|
A | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-46-4398T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1829897 | ||||||
chr1:1830255
|
A | ATAAGT | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-4757_-46-4756i others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830255 | ||||||
chr1:1830265
|
AT | A | 9 | a0001c0001t0001g0197a0001c0001t0001g0329a0001c0001t0003g0290others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-4767delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830265 | ||||||
chr1:1830291
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-4792A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830291 | ||||||
chr1:1830321
|
C | T | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02615.hp2 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-46-4822G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830321 | ||||||
chr1:1830419
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-46-4920C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830419 | ||||||
chr1:1830496
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-46-4997C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830496 | ||||||
chr1:1830538
|
C | T | 1 | a0001c0001t0007g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-46-5039G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830538 | ||||||
chr1:1830566
|
A | T | 89 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-46-5067T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830566 | ||||||
chr1:1830575
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-46-5076A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830575 | ||||||
chr1:1830735
|
C | T | 9 | a0001c0001t0001g0155a0001c0001t0001g0165a0001c0001t0003g0290others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-5236G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830735 | ||||||
chr1:1830792
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-46-5293G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830792 | ||||||
chr1:1830799
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0008g0009 | 3 | HG01243.hp1 HG01255.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-5300C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1830799 | ||||||
chr1:1831000
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0203 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-46-5501G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831000 | ||||||
chr1:1831070
|
T | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18977.hp2 NA19066.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-46-5571A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831070 | ||||||
chr1:1831078
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-5579G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831078 | ||||||
chr1:1831258
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-46-5759C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831258 | ||||||
chr1:1831259
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.-46-5760A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831259 | ||||||
chr1:1831318
|
C | T | 100 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-46-5819G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831318 | ||||||
chr1:1831337
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-5838A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831337 | ||||||
chr1:1831367
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-5868A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831367 | ||||||
chr1:1831509
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-46-6010G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831509 | ||||||
chr1:1831522
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-46-6023G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831522 | ||||||
chr1:1831767
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-46-6268T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1831767 | ||||||
chr1:1832005
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-46-6506C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832005 | ||||||
chr1:1832032
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-46-6533A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832032 | ||||||
chr1:1832063
|
C | CA | 93 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-46-6565dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832063 | ||||||
chr1:1832063
|
C | CAA | 10 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0197others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46-6566_-46-6565d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832063 | ||||||
chr1:1832063
|
CA | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0165a0001c0002t0001g0287others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-6565delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832063 | ||||||
chr1:1832120
|
A | C | 1 | a0001c0002t0001g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-46-6621T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832120 | ||||||
chr1:1832257
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-6758G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832257 | ||||||
chr1:1832335
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0041others(4): Show | 7 | HG00280.hp2 HG00735.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-6836C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832335 | ||||||
chr1:1832487
|
TGAGA | T | 12 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0223others(9): Show | 12 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.-47+6699_-47+6702d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832487 | ||||||
chr1:1832559
|
G | C | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-47+6631C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832559 | ||||||
chr1:1832791
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-47+6399A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832791 | ||||||
chr1:1832934
|
AC | A | 6 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+6255delG | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1832934 | ||||||
chr1:1833196
|
C | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+5994G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1833196 | ||||||
chr1:1833205
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-47+5985T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1833205 | ||||||
chr1:1833388
|
GAA | G | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG03225.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-47+5800_-47+5801d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1833388 | ||||||
chr1:1833630
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02572.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+5560C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1833630 | ||||||
chr1:1834144
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-47+5046A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834144 | ||||||
chr1:1834321
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-47+4869G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834321 | ||||||
chr1:1834444
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-47+4746T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834444 | ||||||
chr1:1834453
|
C | A | 2 | a0001c0001t0001g0197a0001c0001t0013g0196 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-47+4737G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834453 | ||||||
chr1:1834655
|
A | C | 79 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-47+4535T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834655 | ||||||
chr1:1834667
|
C | CT | 112 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(109): Show | 112 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-47+4522dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834667 | ||||||
chr1:1834667
|
C | CTT | 7 | a0001c0001t0001g0128a0001c0001t0001g0206a0001c0001t0001g0211others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+4521_-47+4522d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834667 | ||||||
chr1:1834667
|
CT | C | 8 | a0001c0001t0001g0190a0001c0001t0001g0283a0001c0001t0001g0303others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+4522delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834667 | ||||||
chr1:1834734
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-47+4456A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834734 | ||||||
chr1:1834744
|
G | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+4446C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834744 | ||||||
chr1:1834762
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-47+4428C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834762 | ||||||
chr1:1834814
|
G | A | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-47+4376C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834814 | ||||||
chr1:1834859
|
G | A | 2 | a0001c0001t0001g0191a0001c0003t0001g0249 | 2 | NA18980.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-47+4331C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834859 | ||||||
chr1:1834920
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-47+4270T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1834920 | ||||||
chr1:1835417
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0112 | 2 | HG00642.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.-47+3773T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835417 | ||||||
chr1:1835499
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47+3691G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835499 | ||||||
chr1:1835680
|
T | C | 1 | a0001c0001t0001g0310 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-47+3510A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835680 | ||||||
chr1:1835683
|
A | G | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-47+3507T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835683 | ||||||
chr1:1835735
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-47+3455C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835735 | ||||||
chr1:1835774
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47+3416T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835774 | ||||||
chr1:1835833
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+3357C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835833 | ||||||
chr1:1835893
|
G | A | 6 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+3297C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835893 | ||||||
chr1:1835922
|
G | GA | 87 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0023others(84): Show | 88 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-47+3267dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835922 | ||||||
chr1:1835922
|
G | GAA | 86 | a0001c0001t0001g0035a0001c0001t0001g0119a0001c0001t0001g0121others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-47+3266_-47+3267d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835922 | ||||||
chr1:1835922
|
G | GAAA | 10 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0145others(7): Show | 10 | HG00544.hp2 HG00639.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+3265_-47+3267d others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835922 | ||||||
chr1:1835922
|
GA | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0056a0001c0001t0001g0086others(46): Show | 50 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.-47+3267delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835922 | ||||||
chr1:1835929
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0055others(1): Show | 4 | NA18961.hp1 NA18962.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+3261T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1835929 | ||||||
chr1:1836016
|
G | C | 2 | a0001c0001t0001g0197a0001c0001t0013g0196 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-47+3174C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836016 | ||||||
chr1:1836125
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-47+3065T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836125 | ||||||
chr1:1836126
|
C | A | 111 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-47+3064G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836126 | ||||||
chr1:1836203
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-47+2987G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836203 | ||||||
chr1:1836387
|
CT | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(127): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-47+2802delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836387 | ||||||
chr1:1836387
|
CTT | C | 98 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0075others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-47+2801_-47+2802d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836387 | ||||||
chr1:1836387
|
CTTTT | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+2799_-47+2802d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836387 | ||||||
chr1:1836565
|
T | A | 1 | a0001c0001t0018g0314 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-47+2625A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836565 | ||||||
chr1:1836656
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-47+2534A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836656 | ||||||
chr1:1836856
|
C | CT | 10 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0225others(7): Show | 10 | HG01081.hp1 HG01243.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+2333dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836856 | ||||||
chr1:1836856
|
CT | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(117): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-47+2333delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836856 | ||||||
chr1:1836856
|
CTTTTT | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+2329_-47+2333d others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836856 | ||||||
chr1:1836889
|
G | T | 2 | a0001c0001t0004g0006a0001c0001t0004g0007 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-47+2301C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1836889 | ||||||
chr1:1837006
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47+2184A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837006 | ||||||
chr1:1837182
|
CTG | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+2006_-47+2007d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837182 | ||||||
chr1:1837221
|
C | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-47+1969G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837221 | ||||||
chr1:1837227
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-47+1963T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837227 | ||||||
chr1:1837255
|
A | AT | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0021others(57): Show | 62 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-47+1934dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837255 | ||||||
chr1:1837255
|
AT | A | 10 | a0001c0001t0001g0127a0001c0001t0001g0268a0001c0001t0001g0318others(7): Show | 10 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+1934delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837255 | ||||||
chr1:1837340
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(56): Show | 61 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-47+1850G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837340 | ||||||
chr1:1837371
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+1819A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837371 | ||||||
chr1:1837455
|
C | T | 66 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-47+1735G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837455 | ||||||
chr1:1837545
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-47+1645A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837545 | ||||||
chr1:1837733
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+1457G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837733 | ||||||
chr1:1837911
|
C | T | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+1279G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1837911 | ||||||
chr1:1838109
|
A | G | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47+1081T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838109 | ||||||
chr1:1838235
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-47+955G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838235 | ||||||
chr1:1838346
|
C | G | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47+844G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838346 | ||||||
chr1:1838388
|
A | C | 1 | a0001c0001t0008g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-47+802T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838388 | ||||||
chr1:1838428
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-47+762G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838428 | ||||||
chr1:1838435
|
CT | C | 9 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+754delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838435 | ||||||
chr1:1838449
|
C | CT | 78 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.-47+740dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838449 | ||||||
chr1:1838543
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-47+647G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838543 | ||||||
chr1:1838545
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-47+645G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838545 | ||||||
chr1:1838619
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-47+571A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838619 | ||||||
chr1:1838739
|
C | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+451G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838739 | ||||||
chr1:1838942
|
T | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0133a0001c0001t0001g0136others(1): Show | 4 | HG01261.hp1 HG02698.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+248A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838942 | ||||||
chr1:1838967
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0060others(4): Show | 7 | HG00423.hp2 HG02155.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+223C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838967 | ||||||
chr1:1838990
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+200C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 2/11 | chr1 | 1838990 | ||||||
chr1:1839260
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-22C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839260 | ||||||
chr1:1839298
|
A | G | 8 | a0001c0001t0001g0289a0001c0001t0003g0290a0001c0001t0003g0291others(5): Show | 8 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-60T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839298 | ||||||
chr1:1839322
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0318 | 2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-95-84C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839322 | ||||||
chr1:1839349
|
C | G | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-95-111G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839349 | ||||||
chr1:1839350
|
T | A | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-95-112A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839350 | ||||||
chr1:1839508
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-270G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839508 | ||||||
chr1:1839515
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-277A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839515 | ||||||
chr1:1839519
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-281T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839519 | ||||||
chr1:1839663
|
A | G | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-425T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839663 | ||||||
chr1:1839727
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-95-489C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839727 | ||||||
chr1:1839845
|
A | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-607T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839845 | ||||||
chr1:1839953
|
G | A | 1 | a0001c0002t0001g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-95-715C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1839953 | ||||||
chr1:1840043
|
T | TA | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0063others(58): Show | 63 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.-95-806dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840043 | ||||||
chr1:1840054
|
A | C | 1 | a0001c0001t0001g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-95-816T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840054 | ||||||
chr1:1840233
|
GA | G | 78 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.-95-996delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840233 | ||||||
chr1:1840277
|
C | G | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-1039G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840277 | ||||||
chr1:1840285
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-95-1047A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840285 | ||||||
chr1:1840400
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-95-1162G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840400 | ||||||
chr1:1840454
|
G | A | 1 | a0001c0002t0001g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-95-1216C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840454 | ||||||
chr1:1840914
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-95-1676G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840914 | ||||||
chr1:1840954
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-1716A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840954 | ||||||
chr1:1840971
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-1733T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1840971 | ||||||
chr1:1841049
|
T | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-95-1811A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1841049 | ||||||
chr1:1841065
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-95-1827A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1841065 | ||||||
chr1:1841230
|
C | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0306 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-95-1992G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1841230 | ||||||
chr1:1841296
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-95-2058A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1841296 | ||||||
chr1:1841637
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-95-2399A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1841637 | ||||||
chr1:1841754
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-95-2516G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1841754 | ||||||
chr1:1841995
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-95-2757A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1841995 | ||||||
chr1:1842179
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-2941G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842179 | ||||||
chr1:1842213
|
A | G | 93 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-95-2975T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842213 | ||||||
chr1:1842221
|
C | G | 92 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-95-2983G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842221 | ||||||
chr1:1842226
|
T | C | 91 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-95-2988A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842226 | ||||||
chr1:1842235
|
C | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.-95-2997G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842235 | ||||||
chr1:1842237
|
T | C | 91 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-95-2999A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842237 | ||||||
chr1:1842282
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-95-3044A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842282 | ||||||
chr1:1842333
|
G | A | 90 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-95-3095C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842333 | ||||||
chr1:1842390
|
CCTGCACT others(1758): Show |
C | 1 | a0001c0001t0001g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-95-4917_-95-3153d others(2): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842390 | ||||||
chr1:1842403
|
C | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.-95-3165G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842403 | ||||||
chr1:1842434
|
CA | C | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0003g0290others(6): Show | 9 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-95-3197delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842434 | ||||||
chr1:1842467
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-95-3229G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842467 | ||||||
chr1:1842553
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-3315T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1842553 | ||||||
chr1:1843087
|
T | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG03225.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-95-3849A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843087 | ||||||
chr1:1843338
|
G | A | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-4100C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843338 | ||||||
chr1:1843381
|
A | T | 98 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-95-4143T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843381 | ||||||
chr1:1843600
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 5 | HG02040.hp1 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-95-4362G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843600 | ||||||
chr1:1843691
|
C | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0166 | 3 | HG02145.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-4453G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843691 | ||||||
chr1:1843736
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-95-4498T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843736 | ||||||
chr1:1843766
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-95-4528T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843766 | ||||||
chr1:1843782
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-95-4544T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843782 | ||||||
chr1:1843783
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-95-4545T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843783 | ||||||
chr1:1843986
|
G | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-4748C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1843986 | ||||||
chr1:1844141
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | NA18947.hp1 NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-95-4903C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844141 | ||||||
chr1:1844253
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-95-5015G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844253 | ||||||
chr1:1844367
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-95-5129C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844367 | ||||||
chr1:1844387
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-95-5149A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844387 | ||||||
chr1:1844391
|
CA | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-95-5154delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844391 | ||||||
chr1:1844391
|
CAA | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-5155_-95-5154d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844391 | ||||||
chr1:1844586
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-95-5348G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844586 | ||||||
chr1:1844598
|
A | T | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95-5360T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844598 | ||||||
chr1:1844830
|
C | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(136): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-95-5592G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844830 | ||||||
chr1:1844881
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0008g0009 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-95-5643C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844881 | ||||||
chr1:1844896
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01934.hp2 HG02300.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95-5658G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1844896 | ||||||
chr1:1845139
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-95-5901G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845139 | ||||||
chr1:1845161
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-95-5923G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845161 | ||||||
chr1:1845176
|
A | G | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-95-5938T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845176 | ||||||
chr1:1845299
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-95-6061A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845299 | ||||||
chr1:1845301
|
C | A | 35 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG00423.hp2 HG00673.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-6063G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845301 | ||||||
chr1:1845378
|
C | A | 1 | a0001c0001t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-95-6140G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845378 | ||||||
chr1:1845397
|
C | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0118a0001c0001t0001g0330 | 3 | HG02165.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-95-6159G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845397 | ||||||
chr1:1845400
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-95-6162G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845400 | ||||||
chr1:1845446
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-6208C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845446 | ||||||
chr1:1845551
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0181 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-95-6313A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845551 | ||||||
chr1:1845552
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-95-6314C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845552 | ||||||
chr1:1845568
|
G | A | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-95-6330C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845568 | ||||||
chr1:1845600
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-95-6362T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845600 | ||||||
chr1:1845638
|
T | C | 4 | a0001c0001t0001g0224a0001c0001t0001g0254a0001c0001t0001g0257others(1): Show | 4 | HG01175.hp1 HG01433.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-6400A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845638 | ||||||
chr1:1845812
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-95-6574A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845812 | ||||||
chr1:1845824
|
T | TAC | 23 | a0001c0001t0001g0121a0001c0001t0001g0130a0001c0001t0001g0146others(20): Show | 23 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.-95-6588_-95-6587d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
T | TACAC | 27 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0147others(24): Show | 28 | HG00738.hp1 HG01175.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.-95-6590_-95-6587d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
T | TACACAC | 15 | a0001c0001t0001g0038a0001c0001t0001g0148a0001c0001t0001g0149others(12): Show | 15 | HG02145.hp2 HG02165.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.-95-6592_-95-6587d others(8): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0166a0001c0001t0013g0196 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-95-6596_-95-6587d others(12): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
T | TACACACA others(7): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0039 | 2 | NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-95-6600_-95-6587d others(16): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
TAC | T | 35 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0126others(32): Show | 35 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-6588_-95-6587d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
TACAC | T | 20 | a0001c0001t0001g0123a0001c0001t0001g0128a0001c0001t0001g0129others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.-95-6590_-95-6587d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
TACACAC | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(56): Show | 61 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-95-6592_-95-6587d others(8): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
TACACACA others(3): Show |
T | 1 | a0001c0002t0001g0288 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-95-6596_-95-6587d others(12): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0197a0001c0002t0001g0287 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-95-6598_-95-6587d others(14): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0203a0001c0001t0018g0314 | 2 | HG01123.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-95-6600_-95-6587d others(16): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0044 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-95-6614_-95-6587d others(30): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845824
|
TACACACA others(23): Show |
T | 84 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-95-6616_-95-6587d others(32): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845824 | ||||||
chr1:1845838
|
C | G | 2 | a0001c0001t0001g0194a0001c0001t0007g0008 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-95-6600G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845838 | ||||||
chr1:1845840
|
C | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(53): Show | 58 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-95-6602G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845840 | ||||||
chr1:1845848
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-95-6610G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845848 | ||||||
chr1:1845872
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-95-6634G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845872 | ||||||
chr1:1845957
|
A | G | 1 | a0001c0002t0001g0288 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-95-6719T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1845957 | ||||||
chr1:1846009
|
A | AT | 99 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-95-6772_-95-6771i others(3): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846009 | ||||||
chr1:1846010
|
G | C | 99 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-95-6772C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846010 | ||||||
chr1:1846011
|
G | C | 99 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-95-6773C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846011 | ||||||
chr1:1846151
|
A | G | 1 | a0001c0003t0001g0249 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-95-6913T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846151 | ||||||
chr1:1846428
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-95-7190C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846428 | ||||||
chr1:1846430
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0286 | 2 | HG00738.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-95-7192C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846430 | ||||||
chr1:1846630
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-95-7392G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846630 | ||||||
chr1:1846651
|
T | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(56): Show | 61 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-95-7413A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846651 | ||||||
chr1:1846742
|
T | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95-7504A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846742 | ||||||
chr1:1846922
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-95-7684C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1846922 | ||||||
chr1:1847030
|
A | G | 99 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-95-7792T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847030 | ||||||
chr1:1847144
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | NA18943.hp1 NA18994.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.-95-7906G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847144 | ||||||
chr1:1847293
|
A | ACAACAAA others(10): Show |
6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0204others(3): Show | 6 | HG00735.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.-95-8072_-95-8056d others(19): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847293 | ||||||
chr1:1847597
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-95-8359A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847597 | ||||||
chr1:1847737
|
G | A | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-8499C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847737 | ||||||
chr1:1847748
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-95-8510C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847748 | ||||||
chr1:1847791
|
G | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0023others(9): Show | 12 | HG01258.hp2 HG02293.hp1 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.-95-8553C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847791 | ||||||
chr1:1847792
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-95-8554C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847792 | ||||||
chr1:1847829
|
A | T | 1 | a0001c0001t0007g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-95-8591T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1847829 | ||||||
chr1:1848037
|
C | CTA | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(136): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-95-8801_-95-8800d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848037 | ||||||
chr1:1848090
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-95-8852T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848090 | ||||||
chr1:1848102
|
G | A | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-95-8864C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848102 | ||||||
chr1:1848179
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-95-8941T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848179 | ||||||
chr1:1848221
|
T | TAA | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-8985_-95-8984d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848221 | ||||||
chr1:1848235
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-95-8997G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848235 | ||||||
chr1:1848356
|
GC | G | 63 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.-95-9119delG | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848356 | ||||||
chr1:1848357
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0053 | 2 | NA18961.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-95-9119G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848357 | ||||||
chr1:1848357
|
C | CA | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0156others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-9120dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848357 | ||||||
chr1:1848357
|
C | CAAAA | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-9123_-95-9120d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848357 | ||||||
chr1:1848357
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-95-9119G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848357 | ||||||
chr1:1848357
|
CA | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0087others(165): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-95-9120delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848357 | ||||||
chr1:1848358
|
A | T | 63 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.-95-9120T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848358 | ||||||
chr1:1848388
|
T | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0158 | 2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-95-9150A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848388 | ||||||
chr1:1848405
|
A | T | 1 | a0001c0001t0001g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-95-9167T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848405 | ||||||
chr1:1848475
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-95-9237G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848475 | ||||||
chr1:1848827
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-95-9589A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848827 | ||||||
chr1:1848917
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-95-9679T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1848917 | ||||||
chr1:1849036
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-95-9798A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849036 | ||||||
chr1:1849260
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-95-10022A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849260 | ||||||
chr1:1849278
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-95-10040A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849278 | ||||||
chr1:1849322
|
G | A | 5 | a0001c0001t0001g0205a0001c0001t0001g0217a0001c0001t0001g0226others(2): Show | 5 | NA18942.hp1 NA18952.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-10084C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849322 | ||||||
chr1:1849439
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-95-10201A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849439 | ||||||
chr1:1849555
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-10317C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849555 | ||||||
chr1:1849662
|
A | C | 1 | a0001c0001t0015g0258 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-95-10424T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849662 | ||||||
chr1:1849781
|
T | C | 44 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-95-10543A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849781 | ||||||
chr1:1849906
|
G | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(301): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-95-10668C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849906 | ||||||
chr1:1849992
|
T | TG | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0025others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-95-10755dupC | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1849992 | ||||||
chr1:1850000
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-10762G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850000 | ||||||
chr1:1850017
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-95-10779C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850017 | ||||||
chr1:1850017
|
G | T | 99 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-95-10779C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850017 | ||||||
chr1:1850082
|
C | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0166 | 3 | HG02145.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-10844G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850082 | ||||||
chr1:1850486
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-95-11248A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850486 | ||||||
chr1:1850530
|
G | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-95-11292C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850530 | ||||||
chr1:1850754
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-95-11516A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850754 | ||||||
chr1:1850794
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-95-11556T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850794 | ||||||
chr1:1850837
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0131 | 2 | HG02300.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-95-11599A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850837 | ||||||
chr1:1850866
|
C | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-11628G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850866 | ||||||
chr1:1850979
|
A | G | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-11741T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850979 | ||||||
chr1:1850996
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-95-11758C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1850996 | ||||||
chr1:1851126
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-11888C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851126 | ||||||
chr1:1851171
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-95-11933C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851171 | ||||||
chr1:1851181
|
C | T | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-95-11943G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851181 | ||||||
chr1:1851324
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-95-12086G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851324 | ||||||
chr1:1851336
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-12098C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851336 | ||||||
chr1:1851414
|
G | GA | 9 | a0001c0001t0001g0151a0001c0001t0001g0286a0001c0001t0003g0290others(6): Show | 9 | HG00738.hp1 HG01175.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-12177dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851414 | ||||||
chr1:1851414
|
GA | G | 105 | a0001c0001t0001g0021a0001c0001t0001g0077a0001c0001t0001g0095others(102): Show | 105 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-95-12177delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851414 | ||||||
chr1:1851762
|
G | A | 66 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-95-12524C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851762 | ||||||
chr1:1851781
|
C | T | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-12543G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851781 | ||||||
chr1:1851983
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0013g0196 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-95-12745G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851983 | ||||||
chr1:1851999
|
C | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.-95-12761G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1851999 | ||||||
chr1:1852137
|
A | ATATATAA others(27): Show |
7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-12900_-95-1289 others(38): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852137 | ||||||
chr1:1852145
|
G | A | 66 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-95-12907C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852145 | ||||||
chr1:1852156
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-12918G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852156 | ||||||
chr1:1852251
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-13013G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852251 | ||||||
chr1:1852255
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-13017T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852255 | ||||||
chr1:1852289
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-95-13051G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852289 | ||||||
chr1:1852297
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-95-13059G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852297 | ||||||
chr1:1852386
|
G | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-13148C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852386 | ||||||
chr1:1852427
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-13189A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852427 | ||||||
chr1:1852521
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0166 | 3 | HG02145.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-13283G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852521 | ||||||
chr1:1852544
|
A | T | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-95-13306T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852544 | ||||||
chr1:1852686
|
G | GAAA | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-13451_-95-1344 others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852686 | ||||||
chr1:1852707
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-95-13469C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852707 | ||||||
chr1:1852813
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-95-13575G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1852813 | ||||||
chr1:1853906
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0008g0009 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-95-14668A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1853906 | ||||||
chr1:1854127
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0075 | 2 | NA18992.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-95-14889G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1854127 | ||||||
chr1:1854267
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-95-15029G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1854267 | ||||||
chr1:1854378
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-95-15140T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1854378 | ||||||
chr1:1854694
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-95-15456G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1854694 | ||||||
chr1:1854733
|
G | A | 11 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(8): Show | 11 | HG01243.hp2 HG02258.hp1 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.-95-15495C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1854733 | ||||||
chr1:1854787
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-95-15549G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1854787 | ||||||
chr1:1854876
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-15638A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1854876 | ||||||
chr1:1854898
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-95-15660G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1854898 | ||||||
chr1:1855046
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-95-15808G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855046 | ||||||
chr1:1855138
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-15900T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855138 | ||||||
chr1:1855158
|
C | CA | 35 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG00423.hp2 HG00673.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-15921dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855158 | ||||||
chr1:1855158
|
CA | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-95-15921delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855158 | ||||||
chr1:1855158
|
CAA | C | 8 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(5): Show | 8 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-15922_-95-1592 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855158 | ||||||
chr1:1855245
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(50): Show | 55 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-95-16007C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855245 | ||||||
chr1:1855289
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-95-16051A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855289 | ||||||
chr1:1855321
|
C | CA | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-95-16084dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855321 | ||||||
chr1:1855321
|
C | CAA | 9 | a0001c0001t0001g0039a0001c0001t0002g0308a0001c0001t0002g0321others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-95-16085_-95-1608 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855321 | ||||||
chr1:1855332
|
A | G | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-95-16094T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855332 | ||||||
chr1:1855439
|
C | T | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-16201G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855439 | ||||||
chr1:1855506
|
C | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-16268G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855506 | ||||||
chr1:1855606
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-95-16368G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855606 | ||||||
chr1:1855627
|
C | A | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-95-16389G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855627 | ||||||
chr1:1855670
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-95-16432G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855670 | ||||||
chr1:1855699
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-95-16461C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855699 | ||||||
chr1:1855939
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(50): Show | 55 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-95-16701C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1855939 | ||||||
chr1:1856045
|
G | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-95-16807C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856045 | ||||||
chr1:1856164
|
G | C | 6 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-16926C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856164 | ||||||
chr1:1856295
|
T | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0166 | 3 | HG02145.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-17057A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856295 | ||||||
chr1:1856321
|
G | C | 6 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-17083C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856321 | ||||||
chr1:1856365
|
C | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0204others(3): Show | 6 | HG00735.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.-95-17127G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856365 | ||||||
chr1:1856403
|
C | T | 1 | a0001c0001t0017g0031 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-95-17165G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856403 | ||||||
chr1:1856460
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0045 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-95-17222C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856460 | ||||||
chr1:1856530
|
T | C | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-17292A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856530 | ||||||
chr1:1856642
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02083.hp1 NA18612.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95-17404T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856642 | ||||||
chr1:1856671
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-95-17433G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856671 | ||||||
chr1:1856833
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0023 | 2 | HG01258.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-95-17595A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1856833 | ||||||
chr1:1857246
|
T | TAA | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(50): Show | 55 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-95-18010_-95-1800 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1857246 | ||||||
chr1:1857250
|
C | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(50): Show | 55 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-95-18012G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1857250 | ||||||
chr1:1857305
|
G | GGGCT | 52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(49): Show | 54 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-95-18071_-95-1806 others(8): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1857305 | ||||||
chr1:1857402
|
A | G | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-95-18164T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1857402 | ||||||
chr1:1857404
|
C | A | 1 | a0001c0001t0015g0258 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-95-18166G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1857404 | ||||||
chr1:1857627
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-95-18389T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1857627 | ||||||
chr1:1858116
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-95-18878T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1858116 | ||||||
chr1:1858152
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-95-18914T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1858152 | ||||||
chr1:1858249
|
A | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-19011T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1858249 | ||||||
chr1:1858498
|
TTTGATTC others(4): Show |
T | 1 | a0001c0001t0001g0313 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-95-19271_-95-1926 others(15): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1858498 | ||||||
chr1:1858626
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-95-19388A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1858626 | ||||||
chr1:1858769
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-95-19531C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1858769 | ||||||
chr1:1858828
|
T | G | 13 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(10): Show | 13 | HG01123.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-95-19590A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1858828 | ||||||
chr1:1859002
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-95-19764A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1859002 | ||||||
chr1:1859640
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-95-20402C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1859640 | ||||||
chr1:1859737
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-95-20499C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1859737 | ||||||
chr1:1859774
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-20536G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1859774 | ||||||
chr1:1859783
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-20545C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1859783 | ||||||
chr1:1859787
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-20549T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1859787 | ||||||
chr1:1859812
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-20574G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1859812 | ||||||
chr1:1859830
|
C | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0197a0001c0001t0013g0196 | 3 | HG02559.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-95-20592G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1859830 | ||||||
chr1:1860022
|
G | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0036 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-95-20784C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1860022 | ||||||
chr1:1860372
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-95-21134C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1860372 | ||||||
chr1:1860640
|
C | CA | 8 | a0001c0001t0001g0148a0001c0001t0003g0290a0001c0001t0003g0291others(5): Show | 8 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-21403dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1860640 | ||||||
chr1:1860675
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-21437G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1860675 | ||||||
chr1:1860688
|
G | C | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-95-21450C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1860688 | ||||||
chr1:1860718
|
A | C | 102 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-95-21480T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1860718 | ||||||
chr1:1860776
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01934.hp2 HG02300.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95-21538G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1860776 | ||||||
chr1:1860967
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-21729C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1860967 | ||||||
chr1:1861045
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-95-21807A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861045 | ||||||
chr1:1861056
|
C | T | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-21818G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861056 | ||||||
chr1:1861110
|
C | CA | 112 | a0001c0001t0001g0053a0001c0001t0001g0119a0001c0001t0001g0121others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-95-21873dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861110 | ||||||
chr1:1861110
|
C | CAA | 74 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.-95-21874_-95-2187 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861110 | ||||||
chr1:1861110
|
C | CAAA | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0030others(4): Show | 7 | HG00597.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-21875_-95-2187 others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861110 | ||||||
chr1:1861110
|
CA | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(50): Show | 55 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-95-21873delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861110 | ||||||
chr1:1861230
|
G | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-21992C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861230 | ||||||
chr1:1861269
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-95-22031G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861269 | ||||||
chr1:1861306
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-95-22068T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861306 | ||||||
chr1:1861478
|
T | TAAA | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-22243_-95-2224 others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861478 | ||||||
chr1:1861481
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-95-22243T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861481 | ||||||
chr1:1861563
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-95-22325G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861563 | ||||||
chr1:1861564
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-95-22326T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861564 | ||||||
chr1:1861632
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-95-22394T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861632 | ||||||
chr1:1861672
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-95-22434T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861672 | ||||||
chr1:1861773
|
G | A | 12 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-95-22535C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861773 | ||||||
chr1:1861959
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-95-22721C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1861959 | ||||||
chr1:1862045
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0037others(3): Show | 6 | NA18943.hp1 NA18994.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.-95-22807G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862045 | ||||||
chr1:1862058
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-22820G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862058 | ||||||
chr1:1862082
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-22844A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862082 | ||||||
chr1:1862093
|
A | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0158 | 2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-95-22855T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862093 | ||||||
chr1:1862189
|
T | G | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-22951A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862189 | ||||||
chr1:1862253
|
A | G | 6 | a0001c0001t0001g0130a0001c0001t0001g0208a0001c0001t0001g0218others(3): Show | 6 | HG00673.hp1 HG02056.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.-95-23015T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862253 | ||||||
chr1:1862283
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-95-23045A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862283 | ||||||
chr1:1862332
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-95-23094C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862332 | ||||||
chr1:1862347
|
A | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-95-23109T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862347 | ||||||
chr1:1862405
|
C | T | 8 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-23167G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862405 | ||||||
chr1:1862442
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-95-23204G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862442 | ||||||
chr1:1862471
|
A | ATT | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-23235_-95-2323 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862471 | ||||||
chr1:1862623
|
C | CCT | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-23386_-95-2338 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1862623 | ||||||
chr1:1863545
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0279 | 2 | NA18944.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-95-24307A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1863545 | ||||||
chr1:1863692
|
T | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-24454A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1863692 | ||||||
chr1:1863720
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-95-24482T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1863720 | ||||||
chr1:1863833
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-95-24595A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1863833 | ||||||
chr1:1863854
|
T | C | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02965.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-24616A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1863854 | ||||||
chr1:1863878
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-24640C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1863878 | ||||||
chr1:1863887
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-95-24649A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1863887 | ||||||
chr1:1863953
|
T | A | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-95-24715A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1863953 | ||||||
chr1:1864040
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-24802A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864040 | ||||||
chr1:1864048
|
A | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-95-24810T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864048 | ||||||
chr1:1864230
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-95-24992C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864230 | ||||||
chr1:1864314
|
C | CA | 12 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0156others(9): Show | 12 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-95-25077dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAA | 19 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0057others(16): Show | 19 | HG00735.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-95-25079_-95-2507 others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAA | 71 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-95-25080_-95-2507 others(8): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAA | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(52): Show | 57 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.-95-25081_-95-2507 others(9): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAA | 19 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(16): Show | 19 | HG01517.hp1 HG02080.hp2 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.-95-25082_-95-2507 others(10): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0193a0001c0001t0001g0222a0001c0001t0001g0259others(3): Show | 6 | HG02080.hp1 HG02165.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-25085_-95-2507 others(13): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(3): Show |
10 | a0001c0001t0001g0129a0001c0001t0001g0206a0001c0001t0001g0223others(7): Show | 10 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-95-25086_-95-2507 others(14): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(4): Show |
11 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0131others(8): Show | 11 | HG00408.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-95-25087_-95-2507 others(15): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0128a0001c0001t0001g0254a0001c0001t0001g0257others(3): Show | 6 | HG01175.hp1 HG02738.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-95-25088_-95-2507 others(16): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0244a0001c0001t0001g0263a0001c0001t0001g0318 | 3 | HG02602.hp1 NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-95-25089_-95-2507 others(17): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0278a0001c0001t0001g0309a0001c0002t0001g0295 | 3 | HG02976.hp1 NA18979.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-95-25090_-95-2507 others(18): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0123a0001c0001t0001g0212 | 2 | HG02698.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-95-25091_-95-2507 others(19): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0248a0001c0001t0001g0285a0001c0002t0001g0296 | 3 | HG03239.hp1 HG06807.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-95-25092_-95-2507 others(20): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0261 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-95-25093_-95-2507 others(21): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0208 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-95-25094_-95-2507 others(22): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0262 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-95-25096_-95-2507 others(24): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(14): Show |
4 | a0001c0001t0001g0260a0001c0001t0001g0272a0001c0001t0001g0320others(1): Show | 4 | HG00408.hp1 HG02300.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-25097_-95-2507 others(25): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0313 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-95-25098_-95-2507 others(26): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0250 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(27): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(29): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0216 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(30): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(20): Show |
4 | a0001c0001t0001g0225a0001c0001t0001g0234a0001c0001t0019g0332others(1): Show | 4 | HG01243.hp2 HG01255.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95-25077_-95-2507 others(31): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0210 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(34): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(24): Show |
2 | a0001c0001t0001g0241a0001c0001t0001g0280 | 2 | NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-95-25077_-95-2507 others(35): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0218 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(36): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0312 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(37): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(27): Show |
2 | a0001c0001t0001g0213a0001c0001t0016g0311 | 2 | HG02027.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-95-25077_-95-2507 others(38): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(42): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0252 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(43): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(37): Show |
1 | a0001c0001t0001g0256 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(48): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864314
|
C | CAAAAAAA others(46): Show |
1 | a0001c0001t0001g0214 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-95-25077_-95-2507 others(57): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864314 | ||||||
chr1:1864326
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0002t0001g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-95-25102_-95-2508 others(18): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864326 | ||||||
chr1:1864337
|
G | A | 97 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-95-25099C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864337 | ||||||
chr1:1864350
|
C | T | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-95-25112G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864350 | ||||||
chr1:1864452
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-95-25214G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864452 | ||||||
chr1:1864470
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-25232A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864470 | ||||||
chr1:1864687
|
G | GA | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-25450dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864687 | ||||||
chr1:1864771
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-95-25533T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864771 | ||||||
chr1:1864985
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-25747T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1864985 | ||||||
chr1:1865122
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-96+25698G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865122 | ||||||
chr1:1865177
|
G | A | 44 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-96+25643C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865177 | ||||||
chr1:1865218
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0034 | 2 | HG00099.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-96+25602G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865218 | ||||||
chr1:1865267
|
A | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0329 | 3 | HG01258.hp2 HG02293.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-96+25553T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865267 | ||||||
chr1:1865278
|
A | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(151): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-96+25542T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865278 | ||||||
chr1:1865278
|
ACAAAAAA others(4): Show |
A | 6 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+25531_-96+2554 others(15): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865278 | ||||||
chr1:1865279
|
C | A | 1 | a0001c0001t0001g0209 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-96+25541G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865279 | ||||||
chr1:1865289
|
C | A | 12 | a0001c0001t0001g0021a0001c0001t0001g0205a0001c0001t0001g0211others(9): Show | 12 | HG00140.hp1 HG01243.hp2 HG03486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-96+25531G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865289 | ||||||
chr1:1865290
|
C | CA | 11 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0090others(8): Show | 11 | HG02647.hp2 NA18747.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.-96+25529dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865290 | ||||||
chr1:1865291
|
A | C | 6 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+25529T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865291 | ||||||
chr1:1865345
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-96+25475C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865345 | ||||||
chr1:1865353
|
G | A | 8 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+25467C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865353 | ||||||
chr1:1865376
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-96+25444C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865376 | ||||||
chr1:1865459
|
A | G | 1 | a0001c0001t0002g0321 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-96+25361T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865459 | ||||||
chr1:1865731
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-96+25089G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865731 | ||||||
chr1:1865891
|
G | GTTTT | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+24925_-96+2492 others(8): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865891 | ||||||
chr1:1865901
|
T | G | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-96+24919A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865901 | ||||||
chr1:1865951
|
T | A | 68 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-96+24869A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865951 | ||||||
chr1:1865962
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-96+24858C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865962 | ||||||
chr1:1865999
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-96+24821G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1865999 | ||||||
chr1:1866115
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-96+24705A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866115 | ||||||
chr1:1866132
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+24688C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866132 | ||||||
chr1:1866232
|
G | A | 1 | a0001c0001t0002g0327 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-96+24588C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866232 | ||||||
chr1:1866241
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | NA18947.hp1 NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-96+24579C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866241 | ||||||
chr1:1866258
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-96+24562T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866258 | ||||||
chr1:1866508
|
A | G | 102 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-96+24312T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866508 | ||||||
chr1:1866635
|
T | TA | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(144): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-96+24184dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866635 | ||||||
chr1:1866635
|
T | TAA | 7 | a0001c0001t0001g0032a0001c0001t0001g0055a0001c0001t0001g0095others(4): Show | 7 | HG03688.hp2 HG03710.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+24183_-96+2418 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866635 | ||||||
chr1:1866635
|
T | TAAA | 99 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0123others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-96+24182_-96+2418 others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866635 | ||||||
chr1:1866717
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-96+24103C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1866717 | ||||||
chr1:1867088
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 6 | NA18939.hp1 NA18942.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+23732C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1867088 | ||||||
chr1:1867128
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+23692T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1867128 | ||||||
chr1:1867449
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0165 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-96+23371T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1867449 | ||||||
chr1:1867751
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+23069G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1867751 | ||||||
chr1:1867752
|
G | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-96+23068C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1867752 | ||||||
chr1:1867766
|
A | G | 5 | a0001c0001t0001g0234a0001c0001t0001g0248a0001c0001t0001g0256others(2): Show | 5 | HG01255.hp2 HG02300.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+23054T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1867766 | ||||||
chr1:1867838
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-96+22982A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1867838 | ||||||
chr1:1868261
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-96+22559A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868261 | ||||||
chr1:1868367
|
G | C | 1 | a0001c0001t0001g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-96+22453C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868367 | ||||||
chr1:1868412
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-96+22408C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868412 | ||||||
chr1:1868446
|
A | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+22374T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868446 | ||||||
chr1:1868514
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-96+22306A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868514 | ||||||
chr1:1868557
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-96+22263A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868557 | ||||||
chr1:1868610
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-96+22210C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868610 | ||||||
chr1:1868729
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+22091C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868729 | ||||||
chr1:1868864
|
T | C | 1 | a0001c0001t0002g0328 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-96+21956A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868864 | ||||||
chr1:1868925
|
C | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0229a0001c0001t0001g0233others(2): Show | 5 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+21895G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1868925 | ||||||
chr1:1869117
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-96+21703G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869117 | ||||||
chr1:1869185
|
C | CA | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0033others(81): Show | 86 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.-96+21634dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869185 | ||||||
chr1:1869185
|
C | CAA | 7 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0141others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+21633_-96+2163 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869185 | ||||||
chr1:1869185
|
CA | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 33 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+21634delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869185 | ||||||
chr1:1869327
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-96+21493A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869327 | ||||||
chr1:1869528
|
CCCTGCTT | C | 6 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 6 | NA18939.hp1 NA18942.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+21285_-96+2129 others(11): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869528 | ||||||
chr1:1869595
|
G | A | 62 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.-96+21225C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869595 | ||||||
chr1:1869753
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-96+21067T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869753 | ||||||
chr1:1869957
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-96+20863C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1869957 | ||||||
chr1:1870050
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-96+20770C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1870050 | ||||||
chr1:1870493
|
T | G | 1 | a0001c0002t0001g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-96+20327A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1870493 | ||||||
chr1:1870582
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-96+20238A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1870582 | ||||||
chr1:1870606
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-96+20214A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1870606 | ||||||
chr1:1870613
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-96+20207C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1870613 | ||||||
chr1:1870733
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-96+20087T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1870733 | ||||||
chr1:1870766
|
C | T | 1 | a0001c0001t0009g0040 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-96+20054G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1870766 | ||||||
chr1:1870799
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-96+20021C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1870799 | ||||||
chr1:1871038
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-96+19782G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871038 | ||||||
chr1:1871210
|
G | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(47): Show | 52 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.-96+19610C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871210 | ||||||
chr1:1871226
|
G | A | 2 | a0001c0002t0001g0295a0001c0002t0001g0296 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+19594C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871226 | ||||||
chr1:1871230
|
C | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0079 | 3 | HG02809.hp1 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-96+19590G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871230 | ||||||
chr1:1871277
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-96+19543A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871277 | ||||||
chr1:1871414
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-96+19406G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871414 | ||||||
chr1:1871469
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-96+19351G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871469 | ||||||
chr1:1871789
|
G | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG03225.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-96+19031C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871789 | ||||||
chr1:1871936
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-96+18884A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871936 | ||||||
chr1:1871952
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+18868G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1871952 | ||||||
chr1:1872332
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-96+18488C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1872332 | ||||||
chr1:1872341
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+18479G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1872341 | ||||||
chr1:1872405
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-96+18415C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1872405 | ||||||
chr1:1872528
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-96+18292A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1872528 | ||||||
chr1:1872544
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-96+18276G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1872544 | ||||||
chr1:1872863
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-96+17957G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1872863 | ||||||
chr1:1872987
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+17833G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1872987 | ||||||
chr1:1872990
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0060others(4): Show | 7 | HG00423.hp2 HG02155.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+17830A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1872990 | ||||||
chr1:1873080
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-96+17740C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1873080 | ||||||
chr1:1873144
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-96+17676G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1873144 | ||||||
chr1:1873213
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-96+17607T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1873213 | ||||||
chr1:1873340
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+17480A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1873340 | ||||||
chr1:1873627
|
G | A | 1 | a0001c0001t0008g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-96+17193C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1873627 | ||||||
chr1:1873782
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-96+17038G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1873782 | ||||||
chr1:1873911
|
T | C | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-96+16909A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1873911 | ||||||
chr1:1873952
|
G | A | 84 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-96+16868C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1873952 | ||||||
chr1:1874188
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-96+16632A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874188 | ||||||
chr1:1874257
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-96+16563G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874257 | ||||||
chr1:1874335
|
T | C | 8 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-96+16485A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874335 | ||||||
chr1:1874419
|
G | C | 7 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+16401C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874419 | ||||||
chr1:1874481
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-96+16339G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874481 | ||||||
chr1:1874605
|
T | TA | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(100): Show | 105 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-96+16214dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874605 | ||||||
chr1:1874605
|
T | TAA | 56 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0100others(53): Show | 56 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-96+16213_-96+1621 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874605 | ||||||
chr1:1874605
|
T | TAAA | 11 | a0001c0001t0001g0130a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG02080.hp1 HG02155.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.-96+16212_-96+1621 others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874605 | ||||||
chr1:1874605
|
TA | T | 86 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.-96+16214delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874605 | ||||||
chr1:1874681
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-96+16139G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874681 | ||||||
chr1:1874856
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+15964G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874856 | ||||||
chr1:1874867
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-96+15953T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874867 | ||||||
chr1:1874894
|
T | C | 1 | a0001c0001t0013g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-96+15926A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874894 | ||||||
chr1:1874912
|
T | G | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-96+15908A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874912 | ||||||
chr1:1874925
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-96+15895C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1874925 | ||||||
chr1:1875008
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-96+15812C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875008 | ||||||
chr1:1875010
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-96+15810C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875010 | ||||||
chr1:1875038
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02572.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+15782G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875038 | ||||||
chr1:1875109
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-96+15711G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875109 | ||||||
chr1:1875121
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0060others(4): Show | 7 | HG00423.hp2 HG02155.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+15699C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875121 | ||||||
chr1:1875130
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-96+15690C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875130 | ||||||
chr1:1875208
|
T | C | 101 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-96+15612A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875208 | ||||||
chr1:1875267
|
C | A | 2 | a0001c0002t0001g0295a0001c0002t0001g0296 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+15553G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875267 | ||||||
chr1:1875382
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-96+15438C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875382 | ||||||
chr1:1875435
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-96+15385G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875435 | ||||||
chr1:1875439
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-96+15381G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875439 | ||||||
chr1:1875651
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0277a0001c0001t0001g0318others(1): Show | 4 | NA18951.hp2 NA18960.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+15169C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875651 | ||||||
chr1:1875706
|
T | TTCAACCT others(3): Show |
1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+15104_-96+1511 others(14): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875706 | ||||||
chr1:1875837
|
TC | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(322): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-96+14982delG | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875837 | ||||||
chr1:1875846
|
C | G | 2 | a0001c0001t0001g0148a0001c0001t0008g0009 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-96+14974G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875846 | ||||||
chr1:1875856
|
T | C | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-96+14964A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875856 | ||||||
chr1:1875883
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+14937G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875883 | ||||||
chr1:1875889
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+14931A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875889 | ||||||
chr1:1875912
|
T | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-96+14908A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1875912 | ||||||
chr1:1876049
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-96+14771G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876049 | ||||||
chr1:1876237
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-96+14583A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876237 | ||||||
chr1:1876284
|
T | G | 14 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(11): Show | 14 | HG01123.hp2 HG02145.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+14536A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876284 | ||||||
chr1:1876381
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-96+14439C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876381 | ||||||
chr1:1876457
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-96+14363T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876457 | ||||||
chr1:1876492
|
C | CGA | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0088others(59): Show | 64 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-96+14326_-96+1432 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
C | CGAGA | 22 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(19): Show | 22 | HG00423.hp2 HG00673.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.-96+14324_-96+1432 others(8): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
C | CGAGAGA | 4 | a0001c0001t0001g0041a0001c0001t0001g0107a0001c0001t0001g0197others(1): Show | 4 | HG01081.hp1 HG02559.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+14322_-96+1432 others(10): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
C | CGAGAGAG others(1): Show |
52 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.-96+14320_-96+1432 others(12): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
C | CGAGAGAG others(3): Show |
3 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0009g0040 | 3 | HG01099.hp2 HG01433.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-96+14318_-96+1432 others(14): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
C | CGAGAGAG others(5): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0327 | 3 | HG01516.hp2 HG01517.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-96+14316_-96+1432 others(16): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
C | CGAGAGAG others(7): Show |
1 | a0001c0001t0002g0321 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-96+14314_-96+1432 others(18): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
C | CGAGAGAG others(11): Show |
5 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+14310_-96+1432 others(22): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
C | CGAGAGAG others(15): Show |
1 | a0001c0001t0002g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-96+14306_-96+1432 others(26): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876492
|
CGA | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0289others(1): Show | 4 | HG02451.hp2 HG02738.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+14326_-96+1432 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876492 | ||||||
chr1:1876514
|
A | AGAGAGAG others(9): Show |
1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-96+14305_-96+1430 others(20): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876514 | ||||||
chr1:1876516
|
C | CGT | 6 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(3): Show | 6 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+14303_-96+1430 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876516 | ||||||
chr1:1876516
|
C | T | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-96+14304G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876516 | ||||||
chr1:1876539
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG02572.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+14281C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876539 | ||||||
chr1:1876716
|
T | G | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-96+14104A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876716 | ||||||
chr1:1876930
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-96+13890T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876930 | ||||||
chr1:1876940
|
C | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+13880G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1876940 | ||||||
chr1:1877063
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+13757C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877063 | ||||||
chr1:1877280
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0330 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-96+13540T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877280 | ||||||
chr1:1877298
|
CA | C | 9 | a0001c0001t0001g0172a0001c0001t0001g0197a0001c0001t0001g0209others(6): Show | 9 | HG00438.hp1 HG02074.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.-96+13521delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877298 | ||||||
chr1:1877298
|
CAA | C | 7 | a0001c0001t0001g0212a0001c0001t0003g0290a0001c0001t0003g0291others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+13520_-96+1352 others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877298 | ||||||
chr1:1877310
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-96+13510T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877310 | ||||||
chr1:1877312
|
A | AT | 11 | a0001c0001t0001g0075a0001c0001t0001g0110a0001c0001t0001g0118others(8): Show | 11 | HG01192.hp2 HG02165.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-96+13507_-96+1350 others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877312 | ||||||
chr1:1877312
|
A | T | 52 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0017others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.-96+13508T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877312 | ||||||
chr1:1877314
|
A | AT | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(41): Show | 46 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.-96+13505_-96+1350 others(5): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877314 | ||||||
chr1:1877314
|
A | T | 120 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-96+13506T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877314 | ||||||
chr1:1877316
|
A | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(200): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-96+13504T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877316 | ||||||
chr1:1877328
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0253 | 2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-96+13492A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877328 | ||||||
chr1:1877330
|
T | C | 120 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-96+13490A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877330 | ||||||
chr1:1877344
|
G | C | 1 | a0001c0001t0001g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-96+13476C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877344 | ||||||
chr1:1877391
|
T | C | 1 | a0001c0001t0012g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-96+13429A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877391 | ||||||
chr1:1877465
|
T | A | 8 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0323others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+13355A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877465 | ||||||
chr1:1877684
|
G | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+13136C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1877684 | ||||||
chr1:1878070
|
C | T | 75 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.-96+12750G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878070 | ||||||
chr1:1878215
|
C | A | 7 | a0001c0001t0001g0145a0001c0001t0001g0262a0001c0001t0001g0310others(4): Show | 7 | HG00438.hp2 HG00544.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+12605G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878215 | ||||||
chr1:1878462
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-96+12358G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878462 | ||||||
chr1:1878476
|
A | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG03225.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-96+12344T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878476 | ||||||
chr1:1878620
|
T | C | 1 | a0001c0001t0013g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-96+12200A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878620 | ||||||
chr1:1878629
|
GGTAACAT others(4): Show |
G | 2 | a0001c0001t0001g0260a0001c0001t0001g0278 | 2 | NA19000.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-96+12180_-96+1219 others(15): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878629 | ||||||
chr1:1878641
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0278 | 2 | NA19000.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-96+12179G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878641 | ||||||
chr1:1878651
|
C | T | 84 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-96+12169G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878651 | ||||||
chr1:1878780
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-96+12040A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1878780 | ||||||
chr1:1879162
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-96+11658C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879162 | ||||||
chr1:1879182
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-96+11638G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879182 | ||||||
chr1:1879344
|
C | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0008g0009 | 3 | HG01243.hp1 HG01255.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-96+11476G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879344 | ||||||
chr1:1879403
|
T | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0277a0001c0001t0001g0318others(1): Show | 4 | NA18951.hp2 NA18960.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+11417A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879403 | ||||||
chr1:1879413
|
A | T | 1 | a0001c0001t0013g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-96+11407T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879413 | ||||||
chr1:1879450
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-96+11370A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879450 | ||||||
chr1:1879488
|
C | T | 8 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-96+11332G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879488 | ||||||
chr1:1879492
|
A | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+11328T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879492 | ||||||
chr1:1879548
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11272A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879548 | ||||||
chr1:1879552
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11268T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879552 | ||||||
chr1:1879553
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11267T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879553 | ||||||
chr1:1879554
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11266T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879554 | ||||||
chr1:1879560
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11260G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879560 | ||||||
chr1:1879566
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11254C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879566 | ||||||
chr1:1879567
|
T | C | 102 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-96+11253A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879567 | ||||||
chr1:1879570
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11250A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879570 | ||||||
chr1:1879580
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11240G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879580 | ||||||
chr1:1879587
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-96+11233G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879587 | ||||||
chr1:1879596
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11224A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879596 | ||||||
chr1:1879617
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11203T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879617 | ||||||
chr1:1879618
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11202A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879618 | ||||||
chr1:1879636
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+11184G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879636 | ||||||
chr1:1879651
|
G | C | 1 | a0001c0001t0001g0320 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-96+11169C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879651 | ||||||
chr1:1879659
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-96+11161G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879659 | ||||||
chr1:1879679
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-96+11141A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879679 | ||||||
chr1:1879682
|
G | A | 85 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.-96+11138C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879682 | ||||||
chr1:1879708
|
G | GA | 18 | a0001c0001t0001g0065a0001c0001t0001g0155a0001c0001t0001g0158others(15): Show | 18 | HG01109.hp2 HG01175.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.-96+11111dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879708 | ||||||
chr1:1879929
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+10891C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1879929 | ||||||
chr1:1880171
|
G | C | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | HG02615.hp2 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-96+10649C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880171 | ||||||
chr1:1880191
|
C | A | 2 | a0001c0002t0001g0295a0001c0002t0001g0296 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+10629G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880191 | ||||||
chr1:1880383
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-96+10437C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880383 | ||||||
chr1:1880503
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+10317C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880503 | ||||||
chr1:1880592
|
A | T | 2 | a0001c0001t0001g0135a0001c0001t0020g0333 | 2 | NA18981.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-96+10228T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880592 | ||||||
chr1:1880594
|
A | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(55): Show | 60 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-96+10226T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880594 | ||||||
chr1:1880596
|
T | A | 102 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-96+10224A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880596 | ||||||
chr1:1880889
|
T | C | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+9931A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880889 | ||||||
chr1:1880910
|
T | C | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG03490.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-96+9910A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880910 | ||||||
chr1:1880926
|
CA | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-96+9893delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1880926 | ||||||
chr1:1881006
|
GGA | G | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-96+9812_-96+9813d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881006 | ||||||
chr1:1881065
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(53): Show | 58 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-96+9755C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881065 | ||||||
chr1:1881082
|
C | T | 109 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.-96+9738G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881082 | ||||||
chr1:1881249
|
A | G | 102 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-96+9571T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881249 | ||||||
chr1:1881266
|
G | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-96+9554C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881266 | ||||||
chr1:1881389
|
G | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-96+9431C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881389 | ||||||
chr1:1881428
|
C | CT | 99 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-96+9391dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881428 | ||||||
chr1:1881428
|
C | T | 83 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-96+9392G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881428 | ||||||
chr1:1881552
|
C | T | 7 | a0001c0001t0001g0145a0001c0001t0001g0262a0001c0001t0001g0310others(4): Show | 7 | HG00438.hp2 HG00544.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+9268G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881552 | ||||||
chr1:1881646
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+9174G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881646 | ||||||
chr1:1881695
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 6 | HG01258.hp2 HG02293.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+9125G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881695 | ||||||
chr1:1881696
|
G | T | 1 | a0001c0001t0001g0261 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-96+9124C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881696 | ||||||
chr1:1881798
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(53): Show | 58 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-96+9022G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881798 | ||||||
chr1:1881924
|
A | T | 2 | a0001c0002t0001g0295a0001c0002t0001g0296 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+8896T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881924 | ||||||
chr1:1881984
|
T | C | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+8836A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1881984 | ||||||
chr1:1882054
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | NA19066.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-96+8766C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882054 | ||||||
chr1:1882163
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-96+8657A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882163 | ||||||
chr1:1882263
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-96+8557A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882263 | ||||||
chr1:1882284
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-96+8536A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882284 | ||||||
chr1:1882426
|
CA | C | 128 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-96+8393delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882426 | ||||||
chr1:1882426
|
CAA | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(49): Show | 54 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-96+8392_-96+8393d others(4): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882426 | ||||||
chr1:1882426
|
CAAAAA | C | 97 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-96+8389_-96+8393d others(7): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882426 | ||||||
chr1:1882438
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+8382T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882438 | ||||||
chr1:1882449
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(48): Show | 53 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.-96+8371T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882449 | ||||||
chr1:1882554
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-96+8266C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882554 | ||||||
chr1:1882556
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+8264G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882556 | ||||||
chr1:1882915
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(53): Show | 58 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-96+7905G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882915 | ||||||
chr1:1882920
|
C | CA | 7 | a0001c0001t0001g0020a0001c0001t0001g0088a0001c0001t0001g0108others(4): Show | 7 | HG00544.hp1 HG03041.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+7899dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1882920 | ||||||
chr1:1883086
|
T | G | 5 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0325others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-96+7734A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883086 | ||||||
chr1:1883089
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-96+7731C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883089 | ||||||
chr1:1883172
|
T | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0118a0001c0001t0001g0330 | 3 | HG02165.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-96+7648A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883172 | ||||||
chr1:1883248
|
C | A | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+7572G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883248 | ||||||
chr1:1883249
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+7571T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883249 | ||||||
chr1:1883250
|
G | C | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+7570C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883250 | ||||||
chr1:1883278
|
C | CA | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(55): Show | 60 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-96+7541dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883278 | ||||||
chr1:1883457
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-96+7363A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883457 | ||||||
chr1:1883470
|
A | G | 7 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | NA18939.hp1 NA18940.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+7350T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883470 | ||||||
chr1:1883833
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-96+6987G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883833 | ||||||
chr1:1883911
|
T | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+6909A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883911 | ||||||
chr1:1883967
|
C | CT | 21 | a0001c0001t0001g0121a0001c0001t0001g0127a0001c0001t0001g0128others(18): Show | 21 | HG01109.hp2 HG01891.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.-96+6852dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883967 | ||||||
chr1:1883967
|
CT | C | 6 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG00639.hp1 HG02965.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+6852delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1883967 | ||||||
chr1:1884112
|
T | C | 1 | a0001c0001t0002g0328 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-96+6708A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1884112 | ||||||
chr1:1884132
|
AT | A | 7 | a0001c0001t0001g0186a0001c0001t0001g0198a0001c0001t0001g0268others(4): Show | 7 | HG02145.hp1 HG02735.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+6687delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1884132 | ||||||
chr1:1884183
|
G | A | 84 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-96+6637C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1884183 | ||||||
chr1:1884611
|
C | G | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+6209G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1884611 | ||||||
chr1:1884685
|
CT | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0078a0001c0001t0001g0111others(3): Show | 6 | HG02129.hp1 HG03491.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+6134delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1884685 | ||||||
chr1:1884776
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-96+6044C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1884776 | ||||||
chr1:1884840
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-96+5980C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1884840 | ||||||
chr1:1884979
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0313 | 2 | HG00408.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-96+5841C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1884979 | ||||||
chr1:1885174
|
A | T | 2 | a0001c0001t0001g0197a0001c0001t0013g0196 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-96+5646T>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885174 | ||||||
chr1:1885178
|
G | C | 4 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG00408.hp1 HG02027.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+5642C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885178 | ||||||
chr1:1885179
|
G | C | 4 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG00408.hp1 HG02027.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+5641C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885179 | ||||||
chr1:1885187
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-96+5633G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885187 | ||||||
chr1:1885296
|
T | C | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+5524A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885296 | ||||||
chr1:1885339
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+5481C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885339 | ||||||
chr1:1885444
|
TTAGA | T | 77 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.-96+5372_-96+5375d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885444 | ||||||
chr1:1885523
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+5297G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885523 | ||||||
chr1:1885549
|
A | ATTTTTT | 5 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-96+5270_-96+5271i others(8): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885549 | ||||||
chr1:1885551
|
C | CT | 10 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(7): Show | 10 | HG00735.hp1 HG01175.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+5268dupA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885551 | ||||||
chr1:1885551
|
C | T | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+5269G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885551 | ||||||
chr1:1885551
|
CT | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-96+5268delA | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885551 | ||||||
chr1:1885588
|
G | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+5232C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885588 | ||||||
chr1:1885614
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-96+5206A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885614 | ||||||
chr1:1885731
|
G | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-96+5089C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885731 | ||||||
chr1:1885732
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-96+5088C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885732 | ||||||
chr1:1885761
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-96+5059A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885761 | ||||||
chr1:1885837
|
C | A | 1 | a0001c0001t0001g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-96+4983G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885837 | ||||||
chr1:1885884
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-96+4936G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885884 | ||||||
chr1:1885905
|
T | TAAAACAG others(308): Show |
1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-96+4914_-96+4915i others(317): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885905 | ||||||
chr1:1885905
|
T | TAAAACAG others(315): Show |
1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-96+4914_-96+4915i others(324): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885905 | ||||||
chr1:1885905
|
T | TAAAACAG others(319): Show |
1 | a0001c0001t0007g0008 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-96+4914_-96+4915i others(328): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885905 | ||||||
chr1:1885905
|
T | TAAAACAG others(320): Show |
1 | a0001c0001t0001g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-96+4914_-96+4915i others(329): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885905 | ||||||
chr1:1885905
|
T | TAAAACAG others(321): Show |
4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02970.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+4914_-96+4915i others(330): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885905 | ||||||
chr1:1885949
|
C | A | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+4871G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885949 | ||||||
chr1:1885950
|
A | C | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+4870T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885950 | ||||||
chr1:1885951
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+4869G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1885951 | ||||||
chr1:1886142
|
T | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0131 | 2 | HG02300.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-96+4678A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886142 | ||||||
chr1:1886174
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-96+4646G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886174 | ||||||
chr1:1886211
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG03490.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-96+4609C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886211 | ||||||
chr1:1886267
|
G | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-96+4553C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886267 | ||||||
chr1:1886269
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-96+4551C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886269 | ||||||
chr1:1886271
|
T | A | 1 | a0001c0001t0001g0114 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-96+4549A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886271 | ||||||
chr1:1886370
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-96+4450A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886370 | ||||||
chr1:1886396
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+4424T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886396 | ||||||
chr1:1886397
|
G | T | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+4423C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886397 | ||||||
chr1:1886490
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-96+4330T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886490 | ||||||
chr1:1886690
|
A | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(53): Show | 58 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-96+4130T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886690 | ||||||
chr1:1886745
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-96+4075G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886745 | ||||||
chr1:1886750
|
A | C | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+4070T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886750 | ||||||
chr1:1886751
|
G | A | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+4069C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886751 | ||||||
chr1:1886800
|
G | A | 102 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-96+4020C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886800 | ||||||
chr1:1886807
|
G | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+4013C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886807 | ||||||
chr1:1886830
|
T | A | 7 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+3990A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886830 | ||||||
chr1:1886852
|
C | T | 3 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297 | 3 | HG02258.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+3968G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886852 | ||||||
chr1:1886863
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-96+3957C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886863 | ||||||
chr1:1886879
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-96+3941C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886879 | ||||||
chr1:1886902
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-96+3918T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886902 | ||||||
chr1:1886971
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-96+3849G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886971 | ||||||
chr1:1886991
|
G | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0318 | 2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-96+3829C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1886991 | ||||||
chr1:1887032
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-96+3788A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887032 | ||||||
chr1:1887059
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-96+3761C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887059 | ||||||
chr1:1887206
|
T | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG01192.hp2 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+3614A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887206 | ||||||
chr1:1887257
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-96+3563G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887257 | ||||||
chr1:1887308
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0115 | 3 | HG03491.hp1 HG03492.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-96+3512A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887308 | ||||||
chr1:1887323
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-96+3497C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887323 | ||||||
chr1:1887361
|
T | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317 | 3 | HG03225.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-96+3459A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887361 | ||||||
chr1:1887579
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-96+3241C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887579 | ||||||
chr1:1887799
|
G | C | 1 | a0001c0001t0008g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-96+3021C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887799 | ||||||
chr1:1887939
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-96+2881A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1887939 | ||||||
chr1:1888321
|
G | C | 5 | a0001c0002t0001g0287a0001c0002t0001g0288a0001c0002t0001g0295others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-96+2499C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888321 | ||||||
chr1:1888367
|
C | CA | 9 | a0001c0001t0001g0084a0001c0001t0001g0278a0001c0001t0001g0279others(6): Show | 9 | HG01123.hp2 HG03225.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-96+2452dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888367 | ||||||
chr1:1888381
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+2439T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888381 | ||||||
chr1:1888382
|
A | AG | 52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(49): Show | 54 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-96+2437dupC | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888382 | ||||||
chr1:1888382
|
A | G | 12 | a0001c0001t0001g0092a0001c0001t0001g0132a0001c0001t0001g0319others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-96+2438T>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888382 | ||||||
chr1:1888384
|
G | C | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+2436C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888384 | ||||||
chr1:1888385
|
C | A | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+2435G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888385 | ||||||
chr1:1888444
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-96+2376C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888444 | ||||||
chr1:1888656
|
G | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+2164C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888656 | ||||||
chr1:1888657
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-96+2163C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888657 | ||||||
chr1:1888658
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-96+2162A>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888658 | ||||||
chr1:1888667
|
A | C | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-96+2153T>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888667 | ||||||
chr1:1888762
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+2058G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888762 | ||||||
chr1:1888806
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-96+2014A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888806 | ||||||
chr1:1888903
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-96+1917A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1888903 | ||||||
chr1:1889177
|
T | A | 1 | a0001c0001t0001g0319 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-96+1643A>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889177 | ||||||
chr1:1889227
|
C | A | 1 | a0001c0001t0001g0286 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-96+1593G>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889227 | ||||||
chr1:1889256
|
CTTAA | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG01934.hp2 HG02300.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+1560_-96+1563d others(6): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889256 | ||||||
chr1:1889376
|
G | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-96+1444C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889376 | ||||||
chr1:1889395
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-96+1425A>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889395 | ||||||
chr1:1889659
|
T | TA | 110 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-96+1160dupT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889659 | ||||||
chr1:1889659
|
TA | T | 11 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(8): Show | 11 | HG01069.hp2 HG01516.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-96+1160delT | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889659 | ||||||
chr1:1889921
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-96+899C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889921 | ||||||
chr1:1889952
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-96+868G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1889952 | ||||||
chr1:1890186
|
G | A | 85 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.-96+634C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890186 | ||||||
chr1:1890199
|
G | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0007 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-96+621C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890199 | ||||||
chr1:1890313
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-96+507C>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890313 | ||||||
chr1:1890454
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-96+366C>T | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890454 | ||||||
chr1:1890472
|
C | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0086others(33): Show | 38 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.-96+348G>C | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890472 | ||||||
chr1:1890675
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-96+145G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890675 | ||||||
chr1:1890729
|
G | C | 1 | a0001c0001t0001g0330 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-96+91C>G | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890729 | ||||||
chr1:1890760
|
CCAGGGCG others(29): Show |
C | 1 | a0001c0001t0001g0331 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-96+24_-96+59delCG others(34): Show |
GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890760 | ||||||
chr1:1890770
|
C | T | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-96+50G>A | GNB1 | ENSG00000078369.19 | transcript | ENST00000378609.9 | protein_coding | 1/11 | chr1 | 1890770 |