geneid | 2743 |
---|---|
ensemblid | ENSG00000109738.11 |
hgncid | 4329 |
symbol | GLRB |
name | glycine receptor beta |
refseq_nuc | NM_000824.5 |
refseq_prot | NP_000815.1 |
ensembl_nuc | ENST00000264428.9 |
ensembl_prot | ENSP00000264428.4 |
mane_status | MANE Select |
chr | chr4 |
start | 157076150 |
end | 157172090 |
strand | + |
ver | v1.2 |
region | chr4:157076150-157172090 |
region5000 | chr4:157071150-157177090 |
regionname0 | GLRB_chr4_157076150_157172090 |
regionname5000 | GLRB_chr4_157071150_157177090 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 497 | 302 | 90 | 46 | 135 | 4 | 25 | 103 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0002 | 0/0 | 497 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0003 | 0/0 | 497 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0004 | 0/0 | 497 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0005 | 0/0 | 497 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1494 | 279 | 76 | 46 | 130 | 3 | 23 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
c0002 | 0/0 | 1494 | 14 | 7 | 0 | 4 | 1 | 2 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
c0003 | 1/0 | 1494 | 7 | 6 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
c0004 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
c0005 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
c0006 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
c0007 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
c0008 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
c0009 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1540 | 98 | 14 | 21 | 48 | 2 | 11 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0002 | 0/0 | 1540 | 66 | 8 | 7 | 41 | 1 | 9 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0003 | 0/0 | 1540 | 45 | 29 | 10 | 3 | 0 | 3 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0004 | 0/0 | 1540 | 24 | 0 | 0 | 24 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0005 | 0/0 | 1540 | 15 | 7 | 0 | 7 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0006 | 0/0 | 1540 | 14 | 6 | 1 | 4 | 0 | 3 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0007 | 0/0 | 1540 | 7 | 5 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0008 | 0/0 | 1540 | 6 | 6 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0009 | 0/0 | 1540 | 5 | 0 | 0 | 4 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0010 | 0/0 | 1540 | 3 | 3 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0011 | 0/0 | 1540 | 3 | 0 | 0 | 3 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0012 | 0/0 | 1540 | 3 | 1 | 1 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0013 | 0/0 | 1540 | 3 | 3 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0014 | 0/0 | 1540 | 2 | 1 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0015 | 0/0 | 1540 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0016 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0017 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0018 | 0/0 | 1540 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0019 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0020 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0021 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0022 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0023 | 0/0 | 1540 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0024 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
t0025 | 0/0 | 1540 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1494 | 279 | 76 | 46 | 130 | 3 | 23 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0002 | 0/0 | 1494 | 14 | 7 | 0 | 4 | 1 | 2 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0003 | 1/0 | 1494 | 7 | 6 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0007 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0008 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0002c0004 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0003c0009 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0004c0006 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0005c0005 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3033 | 92 | 9 | 21 | 48 | 2 | 11 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0002 | 0/0 | 3033 | 63 | 8 | 7 | 39 | 1 | 8 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0003 | 0/0 | 3033 | 45 | 29 | 10 | 3 | 0 | 3 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0004 | 0/0 | 3033 | 24 | 0 | 0 | 24 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0005 | 0/0 | 3033 | 15 | 7 | 0 | 7 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0006 | 0/0 | 3033 | 7 | 6 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0007 | 0/0 | 3033 | 7 | 5 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0009 | 0/0 | 3033 | 4 | 0 | 0 | 4 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0010 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0011 | 0/0 | 3033 | 3 | 0 | 0 | 3 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0012 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0013 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0014 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0015 | 0/0 | 3033 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0016 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0017 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0018 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0019 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0020 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0021 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0022 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0023 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0001t0025 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0002t0006 | 0/0 | 3033 | 6 | 0 | 0 | 4 | 0 | 2 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0002t0008 | 0/0 | 3033 | 6 | 6 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0002t0012 | 0/0 | 3033 | 2 | 1 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0003t0001 | 1/0 | 3033 | 6 | 5 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0003t0014 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0007t0002 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0001c0008t0024 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0002c0004t0002 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0003c0009t0009 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0004c0006t0002 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
a0005c0005t0006 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | copy fasta | chr4 | 157071150 | 157177090 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0007g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0011g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0011g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0011g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0012g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0013g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0014g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0015g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0015g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0016g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0017g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0018g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0019g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0020g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0021g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0022g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0023g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0001t0025g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0012g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0002t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0003t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0003t0014g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0007t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0001c0008t0024g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0002c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0003c0009t0009g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0004c0006t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
a0005c0005t0006g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0002 | g0194 | EUR | FIN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00544 | hp2 | a0001 | c0002 | t0006 | g0189 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00639 | hp2 | a0001 | c0001 | t0012 | g0092 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0220 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01255 | hp1 | a0001 | c0001 | t0014 | g0254 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01496 | hp2 | a0001 | c0001 | t0025 | g0121 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01515 | hp1 | a0001 | c0002 | t0012 | g0108 | EUR | IBS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01952 | hp2 | a0001 | c0001 | t0015 | g0187 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0289 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0193 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02015 | hp1 | a0001 | c0002 | t0006 | g0180 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02080 | hp2 | a0001 | c0002 | t0006 | g0181 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02258 | hp2 | a0001 | c0008 | t0024 | g0287 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02280 | hp1 | a0001 | c0002 | t0008 | g0164 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02293 | hp2 | a0001 | c0001 | t0015 | g0240 | AMR | PEL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0116 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0162 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0250 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0256 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02683 | hp1 | a0005 | c0005 | t0006 | g0205 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0168 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02735 | hp1 | a0001 | c0002 | t0006 | g0177 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02809 | hp2 | a0001 | c0001 | t0016 | g0176 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0219 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02895 | hp1 | a0001 | c0001 | t0019 | g0241 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0087 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0260 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0262 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0243 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03139 | hp1 | a0001 | c0002 | t0008 | g0163 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0251 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03195 | hp1 | a0001 | c0002 | t0008 | g0024 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03195 | hp2 | a0001 | c0001 | t0021 | g0253 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03225 | hp1 | a0001 | c0002 | t0008 | g0157 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0258 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03486 | hp2 | a0001 | c0001 | t0022 | g0143 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03492 | hp2 | a0003 | c0009 | t0009 | g0107 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0218 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | GWD | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03579 | hp1 | a0001 | c0002 | t0012 | g0154 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03927 | hp1 | a0002 | c0004 | t0002 | g0245 | SAS | BEB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG04115 | hp2 | a0001 | c0002 | t0006 | g0178 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | STU | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18522 | hp1 | a0001 | c0003 | t0014 | g0257 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | CHB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0038 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18939 | hp2 | a0001 | c0001 | t0011 | g0265 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18952 | hp1 | a0001 | c0007 | t0002 | g0186 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18957 | hp2 | a0001 | c0001 | t0011 | g0279 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18971 | hp1 | a0001 | c0001 | t0011 | g0266 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18985 | hp2 | a0001 | c0001 | t0009 | g0075 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18998 | hp2 | a0001 | c0001 | t0023 | g0273 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19030 | hp1 | a0001 | c0002 | t0008 | g0014 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19056 | hp1 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19070 | hp1 | a0001 | c0001 | t0018 | g0235 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19081 | hp2 | a0001 | c0001 | t0009 | g0094 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19082 | hp1 | a0001 | c0002 | t0006 | g0179 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19084 | hp2 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19085 | hp2 | a0004 | c0006 | t0002 | g0200 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | YRI | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | ASW | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0259 | AFR | ASW | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | GIH | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | GIH | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02109 | hp1 | a0001 | c0001 | t0020 | g0175 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02109 | hp2 | a0001 | c0001 | t0017 | g0020 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0169 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG03471 | hp2 | a0001 | c0002 | t0008 | g0023 | AFR | MSL | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
HG06807 | hp2 | a0001 | c0001 | t0013 | g0017 | AFR | USA | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | LWK | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0059 | REF | REF | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0067 | REF | REF | GLRB_chr4_157071150_157177090 | GLRB | chr4 | 157071150 | 157177090 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:157136671
|
G | A | 1 | a0002 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.500G>A | p.Arg167His | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 5/10 | 677/3033 | 500/1494 | 167/497 | chr4 | 157136671 | ||
chr4:157136883
|
A | G | 1 | a0003 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.607A>G | p.Ser203Gly | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/10 | 784/3033 | 607/1494 | 203/497 | chr4 | 157136883 | ||
chr4:157138811
|
G | A | 1 | a0005 | 1 | HG02683.hp1 | missense_variant&splice_region_variant | MODERATE | c.613G>A | p.Gly205Ser | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/10 | 790/3033 | 613/1494 | 205/497 | chr4 | 157138811 | ||
chr4:157170619
|
C | G | 1 | a0004 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1385C>G | p.Ala462Gly | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 1562/3033 | 1385/1494 | 462/497 | chr4 | 157170619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:157143820
|
C | T | 1 | a0001c0008 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.765C>T | p.Cys255Cys | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/10 | 942/3033 | 765/1494 | 255/497 | chr4 | 157143820 | ||
chr4:157143886
|
T | C | 8 | a0001c0001a0001c0002a0001c0007others(5): Show | 299 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(296): Show |
synonymous_variant | LOW | c.831T>C | p.Thr277Thr | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/10 | 1008/3033 | 831/1494 | 277/497 | chr4 | 157143886 | ||
chr4:157152761
|
T | C | 1 | a0001c0002 | 14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
synonymous_variant | LOW | c.948T>C | p.Leu316Leu | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/10 | 1125/3033 | 948/1494 | 316/497 | chr4 | 157152761 | ||
chr4:157152857
|
A | G | 1 | a0001c0007 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1044A>G | p.Ala348Ala | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/10 | 1221/3033 | 1044/1494 | 348/497 | chr4 | 157152857 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:157076225
|
T | C | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(23): Show | 196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-102T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/10 | 1800 | chr4 | 157076225 | |||||
chr4:157076258
|
C | T | 4 | a0001c0001t0004a0001c0001t0011a0001c0001t0023others(1): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/10 | 1767 | chr4 | 157076258 | |||||
chr4:157076270
|
C | T | 1 | a0001c0008t0024 | 1 | HG02258.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/10 | chr4 | 157076270 | ||||||
chr4:157077999
|
G | T | 1 | a0001c0001t0015 | 2 | HG01952.hp2 HG02293.hp2 |
5_prime_UTR_variant | MODIFIER | c.-26G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/10 | 26 | chr4 | 157077999 | |||||
chr4:157078009
|
A | T | 5 | a0001c0001t0010a0001c0001t0014a0001c0001t0021others(2): Show | 7 | HG01255.hp1 HG02647.hp1 HG03195.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-16A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/10 | 16 | chr4 | 157078009 | |||||
chr4:157170761
|
C | T | 1 | a0001c0001t0020 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 33 | chr4 | 157170761 | |||||
chr4:157170851
|
T | C | 1 | a0001c0008t0024 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 123 | chr4 | 157170851 | |||||
chr4:157170888
|
G | A | 5 | a0001c0001t0006a0001c0001t0012a0001c0002t0006others(2): Show | 17 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*160G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 160 | chr4 | 157170888 | |||||
chr4:157170979
|
A | G | 1 | a0001c0001t0025 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 251 | chr4 | 157170979 | |||||
chr4:157171233
|
T | A | 4 | a0001c0001t0010a0001c0001t0016a0001c0001t0017others(1): Show | 6 | HG02109.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*505T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 505 | chr4 | 157171233 | |||||
chr4:157171270
|
T | A | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(23): Show | 188 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*542T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 542 | chr4 | 157171270 | |||||
chr4:157171303
|
T | C | 1 | a0001c0001t0007 | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*575T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 575 | chr4 | 157171303 | |||||
chr4:157171310
|
G | A | 1 | a0001c0001t0018 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 582 | chr4 | 157171310 | |||||
chr4:157171581
|
T | C | 6 | a0001c0001t0006a0001c0001t0012a0001c0002t0006others(3): Show | 23 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*853T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 853 | chr4 | 157171581 | |||||
chr4:157171631
|
T | C | 2 | a0001c0001t0010a0001c0001t0016 | 4 | HG02647.hp1 HG02809.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*903T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 903 | chr4 | 157171631 | |||||
chr4:157171635
|
T | A | 1 | a0001c0008t0024 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*907T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 907 | chr4 | 157171635 | |||||
chr4:157171691
|
T | C | 1 | a0001c0001t0019 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 963 | chr4 | 157171691 | |||||
chr4:157171768
|
A | G | 6 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(3): Show | 58 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1040A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 1040 | chr4 | 157171768 | |||||
chr4:157171909
|
C | T | 6 | a0001c0001t0006a0001c0001t0012a0001c0002t0006others(3): Show | 23 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1181C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 1181 | chr4 | 157171909 | |||||
chr4:157172073
|
A | G | 1 | a0001c0001t0011 | 3 | NA18939.hp2 NA18957.hp2 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1345A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 10/10 | 1345 | chr4 | 157172073 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:157076333
|
G | T | 2 | a0001c0001t0003g0289a0001c0001t0003g0290 | 2 | HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-30+36G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076333 | ||||||
chr4:157076334
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-30+37C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076334 | ||||||
chr4:157076346
|
G | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+49G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076346 | ||||||
chr4:157076392
|
G | A | 1 | a0001c0002t0008g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-30+95G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076392 | ||||||
chr4:157076408
|
G | T | 3 | a0001c0001t0006g0260a0001c0001t0006g0261a0001c0001t0006g0262 | 3 | HG02895.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-30+111G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076408 | ||||||
chr4:157076437
|
C | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+140C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076437 | ||||||
chr4:157076438
|
C | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+141C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076438 | ||||||
chr4:157076458
|
TGCGCGGG others(6): Show |
T | 7 | a0001c0001t0003g0255a0001c0001t0010g0256a0001c0001t0010g0258others(4): Show | 7 | HG01255.hp1 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+169_-30+181del others(13): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076458 | |||||
chr4:157076542
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+245A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076542 | ||||||
chr4:157076568
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+271A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076568 | ||||||
chr4:157076641
|
C | G | 4 | a0001c0001t0010g0256a0001c0001t0010g0258a0001c0001t0010g0259others(1): Show | 4 | HG02647.hp1 HG03486.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+344C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076641 | ||||||
chr4:157076677
|
G | T | 95 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(92): Show | 103 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-30+380G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076677 | ||||||
chr4:157076728
|
C | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+431C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076728 | ||||||
chr4:157076745
|
A | C | 13 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0006g0156others(10): Show | 13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30+448A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076745 | ||||||
chr4:157076757
|
T | TG | 27 | a0001c0001t0001g0155a0001c0001t0004g0001a0001c0001t0004g0263others(24): Show | 30 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-30+460_-30+461ins others(1): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076757 | ||||||
chr4:157076827
|
T | C | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+530T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076827 | ||||||
chr4:157076972
|
T | G | 1 | a0001c0001t0001g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-30+675T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076972 | ||||||
chr4:157076972
|
T | TG | 61 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(58): Show | 64 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-30+689dupG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | |||||
chr4:157076972
|
T | TGG | 68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0105others(65): Show | 74 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-30+688_-30+689dup others(2): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | |||||
chr4:157076972
|
T | TGGG | 23 | a0001c0001t0001g0007a0001c0001t0001g0144a0001c0001t0001g0145others(20): Show | 25 | HG00738.hp2 HG01109.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.-30+687_-30+689dup others(3): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | |||||
chr4:157076972
|
TG | T | 34 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0002g0184others(31): Show | 35 | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.-30+689delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | |||||
chr4:157076972
|
TGG | T | 50 | a0001c0001t0001g0016a0001c0001t0003g0003a0001c0001t0003g0019others(47): Show | 54 | HG00408.hp1 HG00558.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.-30+688_-30+689del others(2): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 157076972 | |||||
chr4:157076980
|
G | A | 14 | a0001c0001t0001g0016a0001c0001t0003g0158a0001c0001t0003g0161others(11): Show | 14 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+683G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076980 | ||||||
chr4:157076980
|
G | GC | 4 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(1): Show | 4 | HG01069.hp1 HG01993.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+683_-30+684ins others(1): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076980 | ||||||
chr4:157076980
|
G | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+683G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076980 | ||||||
chr4:157076985
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+688G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076985 | ||||||
chr4:157076986
|
G | A | 44 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(41): Show | 47 | HG00408.hp1 HG00558.hp1 HG02015.hp1 others(44): Show |
intron_variant | MODIFIER | c.-30+689G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076986 | ||||||
chr4:157076987
|
A | G | 1 | a0001c0001t0002g0221 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-30+690A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157076987 | ||||||
chr4:157077050
|
G | A | 2 | a0001c0001t0004g0263a0001c0001t0004g0264 | 2 | NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-30+753G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077050 | ||||||
chr4:157077067
|
G | T | 2 | a0001c0002t0008g0014a0001c0002t0008g0164 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-30+770G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077067 | ||||||
chr4:157077114
|
G | C | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-30+817G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077114 | ||||||
chr4:157077123
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30+826G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077123 | ||||||
chr4:157077248
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-29-748C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077248 | ||||||
chr4:157077278
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-29-718G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077278 | ||||||
chr4:157077369
|
G | T | 8 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-627G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077369 | ||||||
chr4:157077644
|
T | C | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-29-352T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077644 | ||||||
chr4:157077795
|
C | A | 1 | a0001c0001t0006g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-29-201C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077795 | ||||||
chr4:157077938
|
A | G | 8 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-58A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 1/9 | chr4 | 157077938 | ||||||
chr4:157078150
|
T | A | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
splice_region_variant&intron_variant | LOW | c.122+4T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078150 | ||||||
chr4:157078230
|
A | G | 6 | a0001c0001t0002g0184a0001c0001t0002g0190a0001c0001t0002g0191others(3): Show | 6 | HG01123.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+84A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078230 | ||||||
chr4:157078296
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+150G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078296 | ||||||
chr4:157078302
|
G | A | 3 | a0001c0001t0003g0046a0001c0002t0008g0023a0001c0002t0008g0024 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.122+156G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078302 | ||||||
chr4:157078376
|
T | C | 92 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0008others(89): Show | 99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.122+230T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078376 | ||||||
chr4:157078395
|
CTG | C | 19 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0021others(16): Show | 21 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+251_122+252del others(2): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157078395 | |||||
chr4:157078504
|
G | GT | 10 | a0001c0001t0002g0212a0001c0001t0005g0169a0001c0001t0005g0182others(7): Show | 10 | HG00544.hp2 HG01192.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+367dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157078504 | |||||
chr4:157078513
|
T | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+367T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078513 | ||||||
chr4:157078522
|
C | A | 1 | a0001c0001t0001g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.122+376C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078522 | ||||||
chr4:157078610
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.122+464A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078610 | ||||||
chr4:157078703
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.122+557G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157078703 | ||||||
chr4:157078865
|
CG | C | 8 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+722delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157078865 | |||||
chr4:157079020
|
C | T | 1 | a0001c0001t0003g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.122+874C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079020 | ||||||
chr4:157079056
|
G | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+910G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079056 | ||||||
chr4:157079060
|
C | T | 1 | a0001c0002t0012g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.122+914C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079060 | ||||||
chr4:157079591
|
A | G | 2 | a0001c0001t0005g0169a0001c0001t0005g0182 | 2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.122+1445A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079591 | ||||||
chr4:157079896
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.122+1750C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079896 | ||||||
chr4:157079927
|
G | C | 7 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(4): Show | 7 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+1781G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079927 | ||||||
chr4:157079935
|
G | C | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+1789G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079935 | ||||||
chr4:157079985
|
C | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+1839C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157079985 | ||||||
chr4:157080326
|
A | G | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+2180A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080326 | ||||||
chr4:157080485
|
T | C | 1 | a0001c0002t0008g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.122+2339T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080485 | ||||||
chr4:157080554
|
A | C | 111 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0008others(108): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.122+2408A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080554 | ||||||
chr4:157080703
|
A | G | 3 | a0001c0002t0006g0179a0001c0002t0006g0180a0001c0002t0006g0181 | 3 | HG02015.hp1 HG02080.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.122+2557A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080703 | ||||||
chr4:157080714
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.122+2568C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080714 | ||||||
chr4:157080733
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.122+2587A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080733 | ||||||
chr4:157080758
|
A | G | 1 | a0001c0001t0007g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.122+2612A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080758 | ||||||
chr4:157080768
|
C | A | 4 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+2622C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157080768 | ||||||
chr4:157081040
|
G | C | 80 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0008others(77): Show | 87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+2894G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081040 | ||||||
chr4:157081050
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.122+2904T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081050 | ||||||
chr4:157081059
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0109 | 2 | HG00733.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.122+2913T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081059 | ||||||
chr4:157081193
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3047G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081193 | ||||||
chr4:157081218
|
T | A | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+3072T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081218 | ||||||
chr4:157081417
|
G | A | 6 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(3): Show | 6 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+3271G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081417 | ||||||
chr4:157081659
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3513G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081659 | ||||||
chr4:157081744
|
C | T | 127 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(124): Show | 137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.122+3598C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081744 | ||||||
chr4:157081755
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.122+3609A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081755 | ||||||
chr4:157081925
|
A | G | 1 | a0001c0001t0005g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.122+3779A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081925 | ||||||
chr4:157081949
|
C | G | 1 | a0001c0001t0002g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.122+3803C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081949 | ||||||
chr4:157081973
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3827G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157081973 | ||||||
chr4:157082008
|
T | A | 5 | a0001c0001t0010g0256a0001c0001t0010g0258a0001c0001t0010g0259others(2): Show | 5 | HG02647.hp1 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+3862T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082008 | ||||||
chr4:157082042
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.122+3896A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082042 | ||||||
chr4:157082074
|
A | G | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3928A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082074 | ||||||
chr4:157082133
|
G | A | 288 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.122+3987G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082133 | ||||||
chr4:157082139
|
A | G | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+3993A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082139 | ||||||
chr4:157082213
|
A | G | 80 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0008others(77): Show | 87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+4067A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082213 | ||||||
chr4:157082309
|
A | G | 4 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+4163A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082309 | ||||||
chr4:157082312
|
G | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+4166G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082312 | ||||||
chr4:157082323
|
A | G | 1 | a0001c0001t0002g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.122+4177A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082323 | ||||||
chr4:157082364
|
C | A | 10 | a0001c0001t0003g0046a0001c0001t0003g0049a0001c0001t0003g0255others(7): Show | 10 | HG01255.hp1 HG02559.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+4218C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082364 | ||||||
chr4:157082441
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.122+4295A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082441 | ||||||
chr4:157082456
|
T | G | 1 | a0001c0001t0003g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+4310T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082456 | ||||||
chr4:157082628
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.122+4482A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082628 | ||||||
chr4:157082639
|
T | C | 128 | a0001c0001t0001g0105a0001c0001t0002g0002a0001c0001t0002g0008others(125): Show | 138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.122+4493T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082639 | ||||||
chr4:157082671
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+4525G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082671 | ||||||
chr4:157082685
|
A | G | 37 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0021others(34): Show | 39 | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.122+4539A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082685 | ||||||
chr4:157082964
|
T | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(3): Show | 6 | HG00733.hp2 HG01123.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+4818T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082964 | ||||||
chr4:157082964
|
T | TTA | 23 | a0001c0001t0001g0015a0001c0001t0001g0100a0001c0001t0001g0101others(20): Show | 23 | HG00544.hp1 HG01255.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.122+4843_122+4844d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTATA | 11 | a0001c0001t0003g0046a0001c0001t0003g0158a0001c0001t0003g0161others(8): Show | 11 | HG01081.hp2 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+4841_122+4844d others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTATATA | 13 | a0001c0001t0001g0065a0001c0001t0004g0001a0001c0001t0004g0267others(10): Show | 16 | HG00558.hp1 HG00597.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.122+4839_122+4844d others(8): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTATATAT others(1): Show |
6 | a0001c0001t0004g0272a0001c0001t0004g0274a0001c0001t0004g0275others(3): Show | 6 | HG02080.hp2 NA18965.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+4837_122+4844d others(10): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTATATAT others(3): Show |
7 | a0001c0001t0004g0263a0001c0001t0004g0264a0001c0001t0004g0277others(4): Show | 7 | HG00408.hp1 NA18957.hp2 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+4835_122+4844d others(12): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTATATAT others(5): Show |
4 | a0001c0001t0004g0282a0001c0001t0004g0283a0001c0002t0008g0023others(1): Show | 4 | HG03195.hp1 HG03471.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+4833_122+4844d others(14): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTATATAT others(7): Show |
3 | a0001c0001t0004g0284a0001c0001t0004g0285a0001c0001t0016g0176 | 3 | HG02809.hp2 NA18612.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.122+4831_122+4844d others(16): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+4829_122+4844d others(18): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0004g0286 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.122+4827_122+4844d others(20): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTTTA | 2 | a0001c0001t0001g0006a0001c0001t0005g0171 | 3 | HG01255.hp2 HG01981.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.122+4819_122+4820i others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTTTATA | 6 | a0001c0001t0003g0172a0001c0001t0005g0169a0001c0001t0005g0182others(3): Show | 6 | HG00544.hp2 HG01515.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+4819_122+4820i others(8): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
T | TTTTATAT others(1): Show |
3 | a0001c0001t0003g0173a0001c0001t0003g0174a0001c0001t0003g0183 | 3 | HG02486.hp2 HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.122+4819_122+4820i others(10): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082964
|
TTA | T | 97 | a0001c0001t0001g0050a0001c0001t0001g0072a0001c0001t0001g0082others(94): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.122+4843_122+4844d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157082964 | |||||
chr4:157082966
|
A | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0021others(13): Show | 18 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.122+4820A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157082966 | ||||||
chr4:157083000
|
T | A | 81 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(78): Show | 88 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.122+4854T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083000 | ||||||
chr4:157083042
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+4896C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083042 | ||||||
chr4:157083113
|
G | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+4967G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083113 | ||||||
chr4:157083114
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+4968C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083114 | ||||||
chr4:157083225
|
CAT | C | 9 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(6): Show | 10 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+5082_122+5083d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157083225 | |||||
chr4:157083403
|
T | TG | 127 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(124): Show | 137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.122+5257_122+5258i others(3): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083403 | ||||||
chr4:157083404
|
T | A | 127 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(124): Show | 137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.122+5258T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083404 | ||||||
chr4:157083525
|
A | T | 4 | a0001c0001t0004g0280a0001c0001t0004g0281a0001c0001t0004g0282others(1): Show | 4 | HG00408.hp1 NA18994.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+5379A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083525 | ||||||
chr4:157083532
|
C | T | 19 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0021others(16): Show | 21 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+5386C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083532 | ||||||
chr4:157083533
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.122+5387G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083533 | ||||||
chr4:157083553
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.122+5407T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083553 | ||||||
chr4:157083556
|
T | C | 85 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(82): Show | 92 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.122+5410T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083556 | ||||||
chr4:157083607
|
G | A | 186 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(183): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+5461G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083607 | ||||||
chr4:157083786
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.122+5640A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083786 | ||||||
chr4:157083834
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+5688C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083834 | ||||||
chr4:157083901
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+5755C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157083901 | ||||||
chr4:157084032
|
A | G | 2 | a0001c0001t0002g0209a0001c0001t0019g0241 | 2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.122+5886A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084032 | ||||||
chr4:157084061
|
A | G | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+5915A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084061 | ||||||
chr4:157084146
|
T | G | 1 | a0001c0001t0002g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.122+6000T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084146 | ||||||
chr4:157084251
|
A | G | 81 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(78): Show | 88 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.122+6105A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084251 | ||||||
chr4:157084306
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122+6160C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084306 | ||||||
chr4:157084488
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0099 | 2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.122+6342C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084488 | ||||||
chr4:157084516
|
A | C | 4 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+6370A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084516 | ||||||
chr4:157084525
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.122+6379A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084525 | ||||||
chr4:157084688
|
A | G | 19 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0021others(16): Show | 21 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+6542A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084688 | ||||||
chr4:157084724
|
G | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(76): Show | 86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+6578G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084724 | ||||||
chr4:157084761
|
C | T | 9 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0002t0006g0177others(6): Show | 9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+6615C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084761 | ||||||
chr4:157084810
|
G | A | 8 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+6664G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157084810 | ||||||
chr4:157085130
|
A | G | 1 | a0001c0002t0006g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.122+6984A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085130 | ||||||
chr4:157085175
|
C | G | 2 | a0001c0001t0003g0033a0001c0001t0003g0035 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.122+7029C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085175 | ||||||
chr4:157085182
|
A | G | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+7036A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085182 | ||||||
chr4:157085229
|
G | T | 1 | a0001c0001t0003g0004 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.122+7083G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085229 | ||||||
chr4:157085320
|
C | T | 9 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0002t0006g0177others(6): Show | 9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+7174C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085320 | ||||||
chr4:157085374
|
G | C | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+7228G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085374 | ||||||
chr4:157085411
|
T | C | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+7265T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085411 | ||||||
chr4:157085495
|
G | T | 1 | a0001c0001t0002g0008 | 2 | HG00558.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.122+7349G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085495 | ||||||
chr4:157085680
|
G | A | 8 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+7534G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085680 | ||||||
chr4:157085944
|
T | C | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+7798T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157085944 | ||||||
chr4:157086085
|
T | G | 127 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(124): Show | 137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.122+7939T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086085 | ||||||
chr4:157086101
|
G | A | 83 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(80): Show | 90 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.122+7955G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086101 | ||||||
chr4:157086110
|
G | A | 1 | a0001c0001t0004g0284 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.122+7964G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086110 | ||||||
chr4:157086161
|
G | A | 80 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(77): Show | 87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+8015G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086161 | ||||||
chr4:157086164
|
G | T | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+8018G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086164 | ||||||
chr4:157086200
|
C | T | 2 | a0001c0001t0007g0193a0001c0001t0007g0220 | 2 | HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.122+8054C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086200 | ||||||
chr4:157086350
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.122+8204G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086350 | ||||||
chr4:157086366
|
A | T | 6 | a0001c0001t0004g0263a0001c0001t0004g0264a0001c0001t0004g0271others(3): Show | 6 | NA18612.hp2 NA18951.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+8220A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086366 | ||||||
chr4:157086433
|
T | C | 14 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0052others(11): Show | 14 | HG01952.hp1 HG02135.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.122+8287T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086433 | ||||||
chr4:157086528
|
C | T | 4 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+8382C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086528 | ||||||
chr4:157086529
|
G | A | 8 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+8383G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086529 | ||||||
chr4:157086620
|
A | T | 1 | a0001c0001t0003g0032 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.122+8474A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086620 | ||||||
chr4:157086661
|
C | T | 9 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0002t0006g0177others(6): Show | 9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+8515C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086661 | ||||||
chr4:157086730
|
G | C | 2 | a0001c0001t0003g0049a0001c0001t0005g0080 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.122+8584G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086730 | ||||||
chr4:157086797
|
C | T | 5 | a0001c0001t0003g0170a0001c0001t0003g0173a0001c0001t0003g0174others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+8651C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157086797 | ||||||
chr4:157087143
|
G | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+8997G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087143 | ||||||
chr4:157087198
|
G | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166others(29): Show | 34 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.122+9052G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087198 | ||||||
chr4:157087255
|
G | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(76): Show | 86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+9109G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087255 | ||||||
chr4:157087323
|
T | C | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+9177T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087323 | ||||||
chr4:157087417
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.122+9271T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087417 | ||||||
chr4:157087580
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.122+9434C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087580 | ||||||
chr4:157087632
|
C | G | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+9486C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087632 | ||||||
chr4:157087673
|
G | GGTA | 9 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0002t0006g0177others(6): Show | 9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+9528_122+9530d others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157087673 | |||||
chr4:157087744
|
C | G | 9 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(6): Show | 10 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+9598C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087744 | ||||||
chr4:157087773
|
T | C | 2 | a0001c0001t0010g0256a0001c0003t0014g0257 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.122+9627T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087773 | ||||||
chr4:157087787
|
C | CT | 78 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(75): Show | 85 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.122+9651dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157087787 | |||||
chr4:157087852
|
G | A | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+9706G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087852 | ||||||
chr4:157087859
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.122+9713A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087859 | ||||||
chr4:157087959
|
T | C | 1 | a0001c0001t0005g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.122+9813T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157087959 | ||||||
chr4:157088043
|
T | C | 2 | a0001c0001t0002g0203a0001c0001t0002g0230 | 2 | HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.122+9897T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088043 | ||||||
chr4:157088126
|
A | C | 2 | a0001c0001t0015g0187a0001c0001t0015g0240 | 2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.122+9980A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088126 | ||||||
chr4:157088217
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+10071G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088217 | ||||||
chr4:157088281
|
TG | T | 18 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0006g0156others(15): Show | 18 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.122+10138delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157088281 | |||||
chr4:157088417
|
C | A | 13 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0006g0156others(10): Show | 13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+10271C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088417 | ||||||
chr4:157088530
|
G | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+10384G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088530 | ||||||
chr4:157088644
|
A | C | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+10498A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088644 | ||||||
chr4:157088700
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.122+10554A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088700 | ||||||
chr4:157088704
|
C | T | 13 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0006g0156others(10): Show | 13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+10558C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088704 | ||||||
chr4:157088850
|
A | T | 2 | a0001c0001t0002g0212a0001c0001t0009g0077 | 2 | NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.122+10704A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088850 | ||||||
chr4:157088866
|
A | G | 8 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+10720A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088866 | ||||||
chr4:157088878
|
T | A | 1 | a0001c0001t0004g0280 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122+10732T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088878 | ||||||
chr4:157088879
|
A | T | 1 | a0001c0001t0004g0280 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122+10733A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088879 | ||||||
chr4:157088881
|
T | A | 1 | a0001c0001t0004g0280 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122+10735T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157088881 | ||||||
chr4:157089141
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0209a0001c0001t0019g0241 | 4 | HG02572.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+10995A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089141 | ||||||
chr4:157089162
|
G | A | 2 | a0001c0003t0001g0116a0001c0003t0001g0137 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122+11016G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089162 | ||||||
chr4:157089318
|
G | A | 13 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0006g0156others(10): Show | 13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+11172G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089318 | ||||||
chr4:157089319
|
A | G | 2 | a0001c0001t0004g0001a0001c0001t0004g0276 | 5 | HG00558.hp1 NA18964.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+11173A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089319 | ||||||
chr4:157089501
|
A | C | 1 | a0001c0001t0002g0217 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.122+11355A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089501 | ||||||
chr4:157089841
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+11695C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089841 | ||||||
chr4:157089975
|
G | T | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+11829G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089975 | ||||||
chr4:157089999
|
C | T | 9 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0002t0006g0177others(6): Show | 9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+11853C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157089999 | ||||||
chr4:157090301
|
T | C | 4 | a0001c0003t0001g0058a0001c0003t0001g0087a0001c0003t0001g0116others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+12155T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090301 | ||||||
chr4:157090486
|
G | T | 1 | a0001c0001t0005g0216 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.122+12340G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090486 | ||||||
chr4:157090506
|
G | A | 5 | a0001c0001t0010g0256a0001c0001t0010g0258a0001c0001t0010g0259others(2): Show | 5 | HG02647.hp1 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+12360G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090506 | ||||||
chr4:157090603
|
G | A | 1 | a0001c0001t0007g0193 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.122+12457G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090603 | ||||||
chr4:157090718
|
A | T | 22 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0021others(19): Show | 24 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.122+12572A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090718 | ||||||
chr4:157090912
|
T | C | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+12766T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090912 | ||||||
chr4:157090985
|
A | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(76): Show | 86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+12839A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157090985 | ||||||
chr4:157091017
|
A | C | 1 | a0001c0001t0007g0193 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.122+12871A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091017 | ||||||
chr4:157091164
|
G | A | 186 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(183): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+13018G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091164 | ||||||
chr4:157091197
|
C | T | 3 | a0001c0001t0003g0046a0001c0002t0008g0023a0001c0002t0008g0024 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.122+13051C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091197 | ||||||
chr4:157091205
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+13059A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091205 | ||||||
chr4:157091530
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.122+13384A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091530 | ||||||
chr4:157091613
|
T | C | 5 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+13467T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091613 | ||||||
chr4:157091648
|
G | C | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+13502G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091648 | ||||||
chr4:157091689
|
T | C | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+13543T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091689 | ||||||
chr4:157091690
|
G | C | 8 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+13544G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091690 | ||||||
chr4:157091749
|
C | G | 13 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(10): Show | 13 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+13603C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091749 | ||||||
chr4:157091909
|
G | T | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+13763G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091909 | ||||||
chr4:157091924
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+13778A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157091924 | ||||||
chr4:157092056
|
T | C | 186 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(183): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+13910T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092056 | ||||||
chr4:157092071
|
A | ACT | 186 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(183): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+13926_122+1392 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157092071 | |||||
chr4:157092160
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122+14014C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092160 | ||||||
chr4:157092291
|
G | C | 186 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(183): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+14145G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092291 | ||||||
chr4:157092414
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122+14268A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092414 | ||||||
chr4:157092416
|
T | G | 186 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(183): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.122+14270T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092416 | ||||||
chr4:157092433
|
G | A | 2 | a0001c0001t0003g0049a0001c0001t0005g0080 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.122+14287G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092433 | ||||||
chr4:157092439
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.122+14293G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092439 | ||||||
chr4:157092529
|
A | G | 13 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0006g0156others(10): Show | 13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+14383A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092529 | ||||||
chr4:157092740
|
G | A | 4 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+14594G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092740 | ||||||
chr4:157092793
|
G | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+14647G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092793 | ||||||
chr4:157092827
|
T | C | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+14681T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092827 | ||||||
chr4:157092910
|
G | A | 13 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0006g0156others(10): Show | 13 | HG01081.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+14764G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092910 | ||||||
chr4:157092954
|
A | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.122+14808A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157092954 | ||||||
chr4:157093062
|
T | C | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.122+14916T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093062 | ||||||
chr4:157093160
|
T | TA | 79 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(76): Show | 86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+15014_122+1501 others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093160 | ||||||
chr4:157093369
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.122+15223C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093369 | ||||||
chr4:157093455
|
T | C | 3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+15309T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093455 | ||||||
chr4:157093460
|
G | A | 6 | a0001c0001t0005g0252a0001c0001t0007g0218a0001c0001t0007g0219others(3): Show | 6 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+15314G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093460 | ||||||
chr4:157093479
|
A | C | 1 | a0001c0001t0002g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.122+15333A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093479 | ||||||
chr4:157093615
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+15469C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093615 | ||||||
chr4:157093733
|
C | T | 79 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(76): Show | 86 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.122+15587C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093733 | ||||||
chr4:157093754
|
C | CA | 35 | a0001c0001t0002g0165a0001c0001t0002g0184a0001c0001t0002g0203others(32): Show | 36 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.122+15632dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157093754 | |||||
chr4:157093754
|
C | CAA | 15 | a0001c0001t0002g0190a0001c0001t0003g0004a0001c0001t0003g0037others(12): Show | 16 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.122+15631_122+1563 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157093754 | |||||
chr4:157093754
|
CA | C | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(81): Show | 87 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+15632delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157093754 | |||||
chr4:157093754
|
CAAAAAA | C | 23 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(20): Show | 26 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.122+15627_122+1563 others(10): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157093754 | |||||
chr4:157093826
|
G | C | 126 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(123): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.122+15680G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093826 | ||||||
chr4:157093889
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+15743G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093889 | ||||||
chr4:157093906
|
T | C | 7 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0122others(4): Show | 7 | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+15760T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157093906 | ||||||
chr4:157094123
|
ACCAATCA others(21): Show |
A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+15979_122+1600 others(32): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157094123 | |||||
chr4:157094169
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16023G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094169 | ||||||
chr4:157094188
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16042G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094188 | ||||||
chr4:157094227
|
A | G | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+16081A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094227 | ||||||
chr4:157094234
|
A | G | 44 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0004g0001others(41): Show | 47 | HG00408.hp1 HG00558.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.122+16088A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094234 | ||||||
chr4:157094343
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.122+16197T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094343 | ||||||
chr4:157094367
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16221A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094367 | ||||||
chr4:157094427
|
GTTTA | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16285_122+1628 others(8): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157094427 | |||||
chr4:157094456
|
C | A | 71 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(68): Show | 78 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.122+16310C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094456 | ||||||
chr4:157094499
|
A | G | 4 | a0001c0001t0003g0026a0001c0001t0003g0073a0001c0001t0003g0074others(1): Show | 4 | HG02145.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+16353A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094499 | ||||||
chr4:157094652
|
G | C | 9 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0002t0006g0177others(6): Show | 9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+16506G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094652 | ||||||
chr4:157094669
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.122+16523A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094669 | ||||||
chr4:157094715
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16569A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094715 | ||||||
chr4:157094766
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16620A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094766 | ||||||
chr4:157094871
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.122+16725C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094871 | ||||||
chr4:157094883
|
CAT | C | 9 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0002t0006g0177others(6): Show | 9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+16738_122+1673 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094883 | ||||||
chr4:157094927
|
T | G | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122+16781T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094927 | ||||||
chr4:157094936
|
T | C | 1 | a0001c0001t0002g0196 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.122+16790T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094936 | ||||||
chr4:157094948
|
T | C | 9 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0002t0006g0177others(6): Show | 9 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+16802T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157094948 | ||||||
chr4:157095045
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+16899A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095045 | ||||||
chr4:157095111
|
G | A | 3 | a0001c0001t0004g0272a0001c0001t0004g0274a0001c0001t0023g0273 | 3 | NA18965.hp1 NA18998.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.122+16965G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095111 | ||||||
chr4:157095180
|
G | C | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+17034G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095180 | ||||||
chr4:157095291
|
GT | G | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+17149delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157095291 | |||||
chr4:157095305
|
C | CA | 37 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0060others(34): Show | 41 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.122+17175dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157095305 | |||||
chr4:157095305
|
CA | C | 8 | a0001c0001t0001g0114a0001c0001t0003g0026a0001c0001t0003g0030others(5): Show | 8 | HG01168.hp2 HG02145.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+17175delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157095305 | |||||
chr4:157095305
|
CAAA | C | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+17173_122+1717 others(7): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157095305 | |||||
chr4:157095363
|
A | C | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+17217A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095363 | ||||||
chr4:157095425
|
C | T | 1 | a0001c0001t0005g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122+17279C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095425 | ||||||
chr4:157095436
|
A | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0149 | 3 | HG02080.hp1 NA18962.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.122+17290A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095436 | ||||||
chr4:157095464
|
C | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+17318C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095464 | ||||||
chr4:157095514
|
A | G | 1 | a0001c0002t0012g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.122+17368A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095514 | ||||||
chr4:157095646
|
G | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0093 | 2 | NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.122+17500G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095646 | ||||||
chr4:157095701
|
G | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+17555G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095701 | ||||||
chr4:157095871
|
T | C | 11 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0001t0014g0254others(8): Show | 11 | HG00544.hp2 HG01255.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+17725T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095871 | ||||||
chr4:157095876
|
C | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+17730C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095876 | ||||||
chr4:157095995
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.122+17849G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157095995 | ||||||
chr4:157096069
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+17923G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096069 | ||||||
chr4:157096256
|
C | A | 25 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(22): Show | 26 | HG00544.hp2 HG01255.hp1 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.122+18110C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096256 | ||||||
chr4:157096404
|
T | C | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18258T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096404 | ||||||
chr4:157096575
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18429A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096575 | ||||||
chr4:157096716
|
A | G | 1 | a0001c0001t0013g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.122+18570A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096716 | ||||||
chr4:157096726
|
T | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0152 | 3 | HG00280.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.122+18580T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096726 | ||||||
chr4:157096760
|
A | G | 6 | a0001c0001t0004g0263a0001c0001t0004g0264a0001c0001t0004g0271others(3): Show | 6 | NA18612.hp2 NA18951.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+18614A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096760 | ||||||
chr4:157096811
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18665G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096811 | ||||||
chr4:157096844
|
C | A | 2 | a0001c0001t0002g0234a0001c0001t0002g0248 | 2 | NA18961.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.122+18698C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096844 | ||||||
chr4:157096866
|
G | A | 1 | a0001c0001t0005g0169 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122+18720G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096866 | ||||||
chr4:157096882
|
T | C | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18736T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096882 | ||||||
chr4:157096979
|
T | A | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122+18833T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096979 | ||||||
chr4:157096991
|
A | G | 7 | a0001c0001t0003g0036a0001c0001t0003g0039a0001c0001t0003g0040others(4): Show | 7 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+18845A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157096991 | ||||||
chr4:157097014
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.122+18868T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097014 | ||||||
chr4:157097028
|
A | G | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.122+18882A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097028 | ||||||
chr4:157097121
|
T | C | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+18975T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097121 | ||||||
chr4:157097241
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057 | 3 | NA18939.hp1 NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.122+19095A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097241 | ||||||
chr4:157097326
|
C | T | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+19180C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097326 | ||||||
chr4:157097416
|
T | G | 1 | a0001c0001t0002g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122+19270T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097416 | ||||||
chr4:157097445
|
A | G | 1 | a0001c0002t0012g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.122+19299A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097445 | ||||||
chr4:157097458
|
G | C | 2 | a0001c0001t0002g0208a0005c0005t0006g0205 | 2 | HG02683.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.122+19312G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097458 | ||||||
chr4:157097459
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.122+19313C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097459 | ||||||
chr4:157097524
|
C | G | 27 | a0001c0001t0003g0288a0001c0001t0004g0001a0001c0001t0004g0263others(24): Show | 30 | HG00408.hp1 HG00558.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.122+19378C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097524 | ||||||
chr4:157097574
|
C | T | 1 | a0001c0001t0003g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122+19428C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097574 | ||||||
chr4:157097665
|
C | A | 1 | a0001c0001t0010g0258 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.122+19519C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097665 | ||||||
chr4:157097818
|
C | T | 22 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(19): Show | 23 | HG01192.hp1 HG01884.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+19672C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097818 | ||||||
chr4:157097849
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.122+19703C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097849 | ||||||
chr4:157097936
|
T | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.122+19790T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097936 | ||||||
chr4:157097969
|
C | T | 3 | a0001c0001t0003g0046a0001c0002t0008g0023a0001c0002t0008g0024 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.122+19823C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097969 | ||||||
chr4:157097970
|
G | A | 7 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(4): Show | 7 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+19824G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097970 | ||||||
chr4:157097972
|
G | T | 1 | a0001c0001t0005g0215 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.122+19826G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097972 | ||||||
chr4:157097998
|
G | C | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122+19852G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157097998 | ||||||
chr4:157098021
|
C | CAA | 16 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(13): Show | 19 | HG00558.hp1 HG02074.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+19886_122+1988 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157098021 | |||||
chr4:157098021
|
C | CAAA | 10 | a0001c0001t0004g0272a0001c0001t0004g0274a0001c0001t0004g0275others(7): Show | 10 | HG00408.hp1 NA18965.hp1 NA18975.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+19885_122+1988 others(7): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157098021 | |||||
chr4:157098473
|
G | A | 2 | a0001c0001t0005g0169a0001c0001t0005g0182 | 2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.122+20327G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098473 | ||||||
chr4:157098592
|
C | T | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+20446C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098592 | ||||||
chr4:157098634
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.122+20488G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098634 | ||||||
chr4:157098634
|
G | T | 1 | a0001c0001t0004g0286 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.122+20488G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098634 | ||||||
chr4:157098657
|
G | C | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122+20511G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098657 | ||||||
chr4:157098677
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.122+20531G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098677 | ||||||
chr4:157098773
|
T | A | 2 | a0001c0001t0002g0197a0001c0001t0002g0229 | 2 | NA18971.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.122+20627T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098773 | ||||||
chr4:157098796
|
C | T | 1 | a0001c0002t0006g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.122+20650C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098796 | ||||||
chr4:157098965
|
G | T | 1 | a0002c0004t0002g0245 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.122+20819G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157098965 | ||||||
chr4:157099082
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.122+20936G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099082 | ||||||
chr4:157099145
|
A | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(280): Show | 299 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.122+20999A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099145 | ||||||
chr4:157099147
|
G | A | 2 | a0001c0001t0005g0025a0001c0001t0005g0080 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.122+21001G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099147 | ||||||
chr4:157099168
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.122+21022A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099168 | ||||||
chr4:157099340
|
CT | C | 46 | a0001c0001t0001g0091a0001c0001t0001g0142a0001c0001t0003g0004others(43): Show | 50 | HG00408.hp1 HG00558.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.123-21201delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157099340 | |||||
chr4:157099357
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-21199G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099357 | ||||||
chr4:157099595
|
C | A | 5 | a0001c0001t0003g0036a0001c0001t0003g0039a0001c0001t0003g0040others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-20961C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099595 | ||||||
chr4:157099834
|
A | AATCATTT others(4): Show |
1 | a0001c0001t0005g0216 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.123-20721_123-2071 others(15): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157099834 | |||||
chr4:157099865
|
TATA | T | 3 | a0001c0001t0002g0202a0001c0001t0002g0227a0001c0001t0002g0228 | 3 | HG02523.hp1 NA18956.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.123-20688_123-2068 others(7): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157099865 | |||||
chr4:157099872
|
T | A | 184 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(181): Show | 196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.123-20684T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099872 | ||||||
chr4:157099876
|
C | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-20680C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099876 | ||||||
chr4:157099898
|
T | C | 1 | a0001c0001t0003g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.123-20658T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099898 | ||||||
chr4:157099910
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.123-20646T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099910 | ||||||
chr4:157099961
|
T | G | 73 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(70): Show | 80 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.123-20595T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099961 | ||||||
chr4:157099999
|
T | A | 1 | a0001c0001t0002g0225 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.123-20557T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157099999 | ||||||
chr4:157100015
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-20541G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100015 | ||||||
chr4:157100117
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-20439T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100117 | ||||||
chr4:157100240
|
C | G | 1 | a0001c0001t0001g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.123-20316C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100240 | ||||||
chr4:157100391
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-20165A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100391 | ||||||
chr4:157100474
|
C | T | 2 | a0001c0001t0004g0263a0001c0001t0004g0264 | 2 | NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.123-20082C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100474 | ||||||
chr4:157100482
|
C | G | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-20074C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100482 | ||||||
chr4:157100648
|
G | A | 1 | a0001c0002t0012g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.123-19908G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100648 | ||||||
chr4:157100731
|
T | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-19825T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100731 | ||||||
chr4:157100811
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0005g0171a0001c0001t0019g0241 | 3 | HG02895.hp1 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.123-19745C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100811 | ||||||
chr4:157100964
|
T | A | 28 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0004g0001others(25): Show | 31 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.123-19592T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157100964 | ||||||
chr4:157101039
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-19517G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101039 | ||||||
chr4:157101130
|
C | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-19426C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101130 | ||||||
chr4:157101298
|
T | C | 30 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(27): Show | 30 | HG00544.hp2 HG00639.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.123-19258T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101298 | ||||||
chr4:157101338
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.123-19218A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101338 | ||||||
chr4:157101395
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.123-19161G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101395 | ||||||
chr4:157101422
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-19134G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101422 | ||||||
chr4:157101469
|
T | A | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-19087T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101469 | ||||||
chr4:157101609
|
G | C | 1 | a0001c0001t0022g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123-18947G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101609 | ||||||
chr4:157101797
|
G | GT | 59 | a0001c0001t0001g0102a0001c0001t0001g0131a0001c0001t0001g0132others(56): Show | 65 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.123-18743dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157101797 | |||||
chr4:157101797
|
GT | G | 29 | a0001c0001t0001g0045a0001c0001t0001g0091a0001c0001t0001g0138others(26): Show | 32 | HG00408.hp1 HG00558.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.123-18743delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157101797 | |||||
chr4:157101819
|
G | C | 1 | a0001c0001t0013g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-18737G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101819 | ||||||
chr4:157101819
|
G | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-18737G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101819 | ||||||
chr4:157101846
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0209 | 3 | HG02572.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-18710C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157101846 | ||||||
chr4:157102065
|
C | A | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-18491C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102065 | ||||||
chr4:157102275
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | NA18939.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.123-18281G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102275 | ||||||
chr4:157102443
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-18113G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102443 | ||||||
chr4:157102622
|
T | C | 1 | a0001c0001t0015g0187 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.123-17934T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102622 | ||||||
chr4:157102750
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.123-17806A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102750 | ||||||
chr4:157102825
|
C | T | 18 | a0001c0001t0001g0113a0001c0001t0003g0161a0001c0001t0006g0156others(15): Show | 18 | HG00544.hp2 HG01081.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.123-17731C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102825 | ||||||
chr4:157102849
|
T | C | 1 | a0005c0005t0006g0205 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123-17707T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102849 | ||||||
chr4:157102853
|
A | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-17703A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102853 | ||||||
chr4:157102981
|
A | G | 26 | a0001c0001t0003g0288a0001c0001t0004g0001a0001c0001t0004g0263others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-17575A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102981 | ||||||
chr4:157102982
|
T | C | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-17574T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157102982 | ||||||
chr4:157103145
|
G | A | 5 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-17411G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103145 | ||||||
chr4:157103157
|
C | CA | 75 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(72): Show | 82 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.123-17383dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157103157 | |||||
chr4:157103161
|
A | C | 14 | a0001c0001t0001g0050a0001c0001t0001g0062a0001c0001t0001g0063others(11): Show | 14 | HG01070.hp1 HG02071.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-17395A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103161 | ||||||
chr4:157103162
|
A | C | 38 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0003g0288others(35): Show | 41 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-17394A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103162 | ||||||
chr4:157103769
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0144 | 2 | HG01123.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.123-16787G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103769 | ||||||
chr4:157103889
|
C | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-16667C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157103889 | ||||||
chr4:157103939
|
T | TTG | 47 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0061others(44): Show | 51 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.123-16595_123-1659 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157103939 | |||||
chr4:157104396
|
G | A | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-16160G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157104396 | ||||||
chr4:157104528
|
G | GT | 34 | a0001c0001t0002g0002a0001c0001t0002g0165a0001c0001t0002g0166others(31): Show | 36 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.123-16018dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157104528 | |||||
chr4:157104942
|
A | G | 2 | a0001c0001t0004g0001a0001c0001t0004g0276 | 5 | HG00558.hp1 NA18964.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-15614A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157104942 | ||||||
chr4:157104979
|
T | C | 1 | a0001c0001t0013g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-15577T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157104979 | ||||||
chr4:157105022
|
T | A | 8 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-15534T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105022 | ||||||
chr4:157105038
|
C | A | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-15518C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105038 | ||||||
chr4:157105065
|
T | G | 2 | a0001c0002t0008g0157a0001c0002t0008g0163 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.123-15491T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105065 | ||||||
chr4:157105075
|
G | A | 1 | a0001c0001t0022g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123-15481G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105075 | ||||||
chr4:157105204
|
C | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0149others(1): Show | 5 | HG02080.hp1 HG02129.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-15352C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105204 | ||||||
chr4:157105595
|
AT | A | 4 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(1): Show | 4 | HG01069.hp1 HG01993.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-14959delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157105595 | |||||
chr4:157105671
|
T | C | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-14885T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105671 | ||||||
chr4:157105766
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.123-14790G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105766 | ||||||
chr4:157105993
|
T | C | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-14563T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157105993 | ||||||
chr4:157106830
|
C | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-13726C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157106830 | ||||||
chr4:157106911
|
C | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-13645C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157106911 | ||||||
chr4:157107092
|
G | A | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-13464G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107092 | ||||||
chr4:157107148
|
C | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-13408C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107148 | ||||||
chr4:157107187
|
C | A | 1 | a0001c0001t0002g0011 | 2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.123-13369C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107187 | ||||||
chr4:157107201
|
G | A | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-13355G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107201 | ||||||
chr4:157107226
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.123-13330C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107226 | ||||||
chr4:157107366
|
T | C | 36 | a0001c0001t0003g0288a0001c0001t0004g0001a0001c0001t0004g0263others(33): Show | 39 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.123-13190T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107366 | ||||||
chr4:157107420
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.123-13136T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107420 | ||||||
chr4:157107480
|
G | A | 3 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269 | 3 | NA18967.hp2 NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.123-13076G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107480 | ||||||
chr4:157107513
|
C | A | 11 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-13043C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107513 | ||||||
chr4:157107522
|
C | T | 1 | a0001c0001t0012g0092 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.123-13034C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107522 | ||||||
chr4:157107583
|
A | G | 1 | a0001c0001t0009g0076 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.123-12973A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107583 | ||||||
chr4:157107722
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.123-12834C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107722 | ||||||
chr4:157107746
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-12810C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107746 | ||||||
chr4:157107848
|
A | C | 1 | a0001c0001t0001g0111 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.123-12708A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157107848 | ||||||
chr4:157108136
|
T | A | 1 | a0001c0001t0003g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.123-12420T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108136 | ||||||
chr4:157108228
|
G | C | 1 | a0001c0001t0011g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.123-12328G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108228 | ||||||
chr4:157108411
|
T | C | 3 | a0001c0001t0010g0256a0001c0001t0010g0258a0001c0001t0010g0259 | 3 | HG02647.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-12145T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108411 | ||||||
chr4:157108441
|
A | AG | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-12115_123-1211 others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108441 | ||||||
chr4:157108627
|
C | T | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-11929C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108627 | ||||||
chr4:157108642
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.123-11914A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108642 | ||||||
chr4:157108728
|
C | T | 43 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(40): Show | 44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.123-11828C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108728 | ||||||
chr4:157108782
|
A | C | 3 | a0001c0001t0003g0019a0001c0001t0003g0031a0001c0001t0003g0048 | 3 | HG00639.hp1 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.123-11774A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157108782 | ||||||
chr4:157109236
|
A | G | 1 | a0001c0001t0016g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.123-11320A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109236 | ||||||
chr4:157109243
|
T | G | 1 | a0001c0001t0003g0068 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.123-11313T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109243 | ||||||
chr4:157109273
|
T | G | 2 | a0001c0002t0008g0157a0001c0002t0008g0163 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.123-11283T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109273 | ||||||
chr4:157109358
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0081others(1): Show | 4 | HG00733.hp2 HG01169.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-11198G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109358 | ||||||
chr4:157109470
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.123-11086C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109470 | ||||||
chr4:157109553
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-11003A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109553 | ||||||
chr4:157109733
|
T | C | 1 | a0001c0002t0006g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.123-10823T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109733 | ||||||
chr4:157109861
|
C | A | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-10695C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109861 | ||||||
chr4:157109936
|
A | G | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-10620A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157109936 | ||||||
chr4:157110074
|
G | A | 1 | a0001c0001t0013g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.123-10482G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110074 | ||||||
chr4:157110078
|
C | T | 8 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-10478C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110078 | ||||||
chr4:157110079
|
G | C | 1 | a0001c0001t0002g0222 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.123-10477G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110079 | ||||||
chr4:157110291
|
T | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-10265T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110291 | ||||||
chr4:157110323
|
C | CTTAAG | 37 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0004g0001others(34): Show | 40 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.123-10231_123-1023 others(9): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157110323 | |||||
chr4:157110363
|
T | C | 2 | a0001c0002t0008g0157a0001c0002t0008g0163 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.123-10193T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110363 | ||||||
chr4:157110429
|
T | A | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-10127T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110429 | ||||||
chr4:157110444
|
T | C | 11 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(8): Show | 11 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-10112T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110444 | ||||||
chr4:157110758
|
C | T | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.123-9798C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110758 | ||||||
chr4:157110759
|
G | T | 1 | a0001c0001t0003g0255 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.123-9797G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110759 | ||||||
chr4:157110805
|
T | C | 37 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0004g0001others(34): Show | 40 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.123-9751T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157110805 | ||||||
chr4:157111125
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123-9431G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111125 | ||||||
chr4:157111243
|
G | C | 38 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0003g0288others(35): Show | 41 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-9313G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111243 | ||||||
chr4:157111420
|
A | G | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-9136A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111420 | ||||||
chr4:157111560
|
G | C | 1 | a0001c0001t0003g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.123-8996G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111560 | ||||||
chr4:157111717
|
A | T | 1 | a0001c0001t0002g0185 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.123-8839A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111717 | ||||||
chr4:157111729
|
G | C | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-8827G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111729 | ||||||
chr4:157111913
|
C | T | 1 | a0005c0005t0006g0205 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123-8643C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157111913 | ||||||
chr4:157112034
|
T | A | 3 | a0001c0001t0010g0256a0001c0001t0010g0258a0001c0001t0010g0259 | 3 | HG02647.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-8522T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112034 | ||||||
chr4:157112076
|
C | CT | 20 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(17): Show | 23 | HG00597.hp2 HG02055.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.123-8469dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157112076 | |||||
chr4:157112076
|
CT | C | 41 | a0001c0001t0001g0064a0001c0001t0001g0099a0001c0001t0001g0141others(38): Show | 45 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.123-8469delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157112076 | |||||
chr4:157112090
|
C | G | 11 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-8466C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112090 | ||||||
chr4:157112169
|
G | A | 2 | a0001c0001t0010g0258a0001c0001t0010g0259 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-8387G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112169 | ||||||
chr4:157112225
|
A | C | 1 | a0001c0001t0001g0050 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.123-8331A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112225 | ||||||
chr4:157112229
|
T | G | 11 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(8): Show | 11 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-8327T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112229 | ||||||
chr4:157112252
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.123-8304A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112252 | ||||||
chr4:157112257
|
G | A | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-8299G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112257 | ||||||
chr4:157112314
|
AT | A | 47 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0003g0170others(44): Show | 50 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.123-8234delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157112314 | |||||
chr4:157112345
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123-8211T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112345 | ||||||
chr4:157112406
|
G | A | 11 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-8150G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112406 | ||||||
chr4:157112529
|
T | A | 8 | a0001c0001t0003g0161a0001c0001t0006g0156a0001c0001t0006g0159others(5): Show | 8 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-8027T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112529 | ||||||
chr4:157112610
|
G | A | 2 | a0001c0002t0008g0157a0001c0002t0008g0163 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.123-7946G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112610 | ||||||
chr4:157112679
|
A | T | 1 | a0001c0001t0002g0237 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.123-7877A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112679 | ||||||
chr4:157112690
|
C | T | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-7866C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112690 | ||||||
chr4:157112773
|
A | C | 1 | a0001c0001t0002g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.123-7783A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112773 | ||||||
chr4:157112873
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.123-7683G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112873 | ||||||
chr4:157112999
|
G | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-7557G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157112999 | ||||||
chr4:157113131
|
A | ATG | 4 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0001t0014g0254others(1): Show | 4 | HG01255.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-7413_123-7412d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157113131 | |||||
chr4:157113235
|
C | T | 2 | a0001c0002t0008g0023a0001c0002t0008g0024 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.123-7321C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113235 | ||||||
chr4:157113243
|
GT | G | 3 | a0001c0001t0005g0252a0001c0001t0007g0250a0001c0001t0007g0251 | 3 | HG02622.hp2 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.123-7311delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157113243 | |||||
chr4:157113260
|
C | T | 2 | a0001c0001t0003g0288a0001c0001t0020g0175 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.123-7296C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113260 | ||||||
chr4:157113267
|
A | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-7289A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113267 | ||||||
chr4:157113418
|
T | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-7138T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113418 | ||||||
chr4:157113445
|
T | C | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-7111T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113445 | ||||||
chr4:157113575
|
T | C | 38 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0003g0288others(35): Show | 41 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-6981T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113575 | ||||||
chr4:157113701
|
A | G | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-6855A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113701 | ||||||
chr4:157113705
|
CA | C | 6 | a0001c0001t0001g0078a0001c0001t0001g0110a0001c0001t0001g0118others(3): Show | 6 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-6850delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113705 | ||||||
chr4:157113859
|
G | C | 1 | a0001c0001t0009g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.123-6697G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113859 | ||||||
chr4:157113914
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0093 | 2 | NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.123-6642G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113914 | ||||||
chr4:157113971
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.123-6585T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157113971 | ||||||
chr4:157114209
|
T | C | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-6347T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114209 | ||||||
chr4:157114341
|
C | CT | 30 | a0001c0001t0001g0078a0001c0001t0001g0118a0001c0001t0001g0122others(27): Show | 33 | HG00408.hp1 HG00558.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.123-6203dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157114341 | |||||
chr4:157114648
|
C | T | 8 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-5908C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114648 | ||||||
chr4:157114666
|
A | G | 92 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(89): Show | 100 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.123-5890A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114666 | ||||||
chr4:157114750
|
T | C | 2 | a0001c0001t0010g0258a0001c0001t0010g0259 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-5806T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114750 | ||||||
chr4:157114876
|
A | ACT | 3 | a0001c0001t0003g0046a0001c0002t0008g0023a0001c0002t0008g0024 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.123-5679_123-5678d others(4): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157114876 | |||||
chr4:157114918
|
C | A | 8 | a0001c0001t0003g0161a0001c0001t0006g0156a0001c0001t0006g0159others(5): Show | 8 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-5638C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114918 | ||||||
chr4:157114937
|
G | A | 70 | a0001c0001t0001g0054a0001c0001t0002g0002a0001c0001t0002g0008others(67): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.123-5619G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114937 | ||||||
chr4:157114943
|
C | G | 26 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-5613C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114943 | ||||||
chr4:157114958
|
A | G | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-5598A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157114958 | ||||||
chr4:157115217
|
C | T | 170 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(167): Show | 182 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.123-5339C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115217 | ||||||
chr4:157115251
|
G | GT | 9 | a0001c0001t0001g0147a0001c0001t0001g0155a0001c0001t0002g0204others(6): Show | 9 | HG01109.hp1 HG01175.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-5287dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157115251 | |||||
chr4:157115251
|
GT | G | 54 | a0001c0001t0001g0034a0001c0001t0001g0084a0001c0001t0001g0118others(51): Show | 55 | HG00408.hp1 HG01192.hp1 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.123-5287delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157115251 | |||||
chr4:157115255
|
T | G | 1 | a0001c0001t0020g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.123-5301T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115255 | ||||||
chr4:157115315
|
T | TA | 99 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(96): Show | 107 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.123-5232dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157115315 | |||||
chr4:157115345
|
A | G | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-5211A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115345 | ||||||
chr4:157115703
|
T | C | 69 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(66): Show | 73 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.123-4853T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115703 | ||||||
chr4:157115730
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.123-4826T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115730 | ||||||
chr4:157115800
|
C | T | 2 | a0001c0001t0004g0274a0001c0001t0023g0273 | 2 | NA18965.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.123-4756C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115800 | ||||||
chr4:157115996
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.123-4560C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115996 | ||||||
chr4:157115996
|
C | T | 13 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(10): Show | 14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-4560C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157115996 | ||||||
chr4:157116237
|
T | C | 77 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0019others(74): Show | 79 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.123-4319T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116237 | ||||||
chr4:157116411
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.123-4145A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116411 | ||||||
chr4:157116422
|
C | T | 1 | a0001c0002t0006g0189 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.123-4134C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116422 | ||||||
chr4:157116437
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.123-4119T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116437 | ||||||
chr4:157116455
|
G | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-4101G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116455 | ||||||
chr4:157116574
|
T | C | 4 | a0001c0001t0003g0161a0001c0001t0006g0156a0001c0001t0006g0159others(1): Show | 4 | HG01081.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-3982T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116574 | ||||||
chr4:157116646
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123-3910A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116646 | ||||||
chr4:157116844
|
G | C | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-3712G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116844 | ||||||
chr4:157116908
|
A | G | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-3648A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157116908 | ||||||
chr4:157117002
|
G | T | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.123-3554G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117002 | ||||||
chr4:157117106
|
G | A | 23 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.123-3450G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117106 | ||||||
chr4:157117213
|
A | G | 7 | a0001c0001t0002g0002a0001c0001t0002g0232a0001c0001t0002g0233others(4): Show | 9 | HG00408.hp2 HG00438.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-3343A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117213 | ||||||
chr4:157117331
|
C | T | 3 | a0001c0001t0003g0046a0001c0002t0008g0023a0001c0002t0008g0024 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.123-3225C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117331 | ||||||
chr4:157117492
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.123-3064G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117492 | ||||||
chr4:157117579
|
G | A | 43 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(40): Show | 44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.123-2977G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117579 | ||||||
chr4:157117769
|
A | G | 1 | a0003c0009t0009g0107 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.123-2787A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117769 | ||||||
chr4:157117805
|
A | G | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-2751A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117805 | ||||||
chr4:157117862
|
T | C | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-2694T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157117862 | ||||||
chr4:157118075
|
G | T | 176 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(173): Show | 188 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.123-2481G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118075 | ||||||
chr4:157118183
|
C | T | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-2373C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118183 | ||||||
chr4:157118311
|
T | A | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-2245T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118311 | ||||||
chr4:157118344
|
G | A | 1 | a0001c0001t0003g0033 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.123-2212G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118344 | ||||||
chr4:157118380
|
C | T | 1 | a0001c0001t0011g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.123-2176C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118380 | ||||||
chr4:157118483
|
C | G | 1 | a0001c0001t0003g0255 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.123-2073C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118483 | ||||||
chr4:157118558
|
A | C | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-1998A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118558 | ||||||
chr4:157118587
|
T | A | 1 | a0001c0001t0021g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.123-1969T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118587 | ||||||
chr4:157118922
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.123-1634A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118922 | ||||||
chr4:157118983
|
G | A | 4 | a0001c0001t0005g0012a0001c0001t0005g0213a0001c0001t0005g0214others(1): Show | 5 | NA18965.hp2 NA18975.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-1573G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157118983 | ||||||
chr4:157119083
|
G | T | 42 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(39): Show | 43 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.123-1473G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119083 | ||||||
chr4:157119087
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.123-1469C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119087 | ||||||
chr4:157119191
|
T | C | 1 | a0001c0001t0002g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123-1365T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119191 | ||||||
chr4:157119237
|
A | G | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-1319A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119237 | ||||||
chr4:157119315
|
T | C | 23 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.123-1241T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119315 | ||||||
chr4:157119328
|
T | C | 30 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(27): Show | 31 | HG01255.hp1 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.123-1228T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119328 | ||||||
chr4:157119687
|
C | A | 3 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0001t0014g0254 | 3 | HG01255.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.123-869C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119687 | ||||||
chr4:157119854
|
G | A | 288 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.123-702G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119854 | ||||||
chr4:157119882
|
G | C | 1 | a0001c0001t0014g0254 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.123-674G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119882 | ||||||
chr4:157119895
|
A | G | 2 | a0001c0001t0003g0044a0001c0001t0003g0070 | 2 | HG02074.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.123-661A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157119895 | ||||||
chr4:157120042
|
G | A | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.123-514G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120042 | ||||||
chr4:157120063
|
G | A | 2 | a0001c0001t0010g0258a0001c0001t0010g0259 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123-493G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120063 | ||||||
chr4:157120089
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.123-467T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120089 | ||||||
chr4:157120126
|
C | T | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.123-430C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120126 | ||||||
chr4:157120127
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123-429G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120127 | ||||||
chr4:157120152
|
G | A | 1 | a0001c0002t0008g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.123-404G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120152 | ||||||
chr4:157120161
|
T | C | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.123-395T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120161 | ||||||
chr4:157120193
|
T | G | 8 | a0001c0001t0003g0161a0001c0001t0006g0156a0001c0001t0006g0159others(5): Show | 8 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-363T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120193 | ||||||
chr4:157120253
|
G | T | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.123-303G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120253 | ||||||
chr4:157120257
|
T | A | 43 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(40): Show | 44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.123-299T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120257 | ||||||
chr4:157120259
|
G | A | 43 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(40): Show | 44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.123-297G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120259 | ||||||
chr4:157120383
|
TAATAATA others(11): Show |
T | 3 | a0001c0001t0001g0083a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | NA18985.hp1 NA19012.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.123-153_123-136del others(18): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157120383 | |||||
chr4:157120386
|
TAATAA | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-154_123-150del others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157120386 | |||||
chr4:157120433
|
G | GA | 30 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(27): Show | 31 | HG01255.hp1 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.123-118dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 157120433 | |||||
chr4:157120439
|
G | A | 177 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(174): Show | 189 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.123-117G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120439 | ||||||
chr4:157120454
|
T | C | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.123-102T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 2/9 | chr4 | 157120454 | ||||||
chr4:157120714
|
A | T | 1 | a0001c0001t0014g0254 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.229+52A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120714 | ||||||
chr4:157120744
|
G | A | 147 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(144): Show | 158 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.229+82G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120744 | ||||||
chr4:157120800
|
T | C | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.229+138T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120800 | ||||||
chr4:157120816
|
A | G | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.229+154A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120816 | ||||||
chr4:157120927
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.229+265C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120927 | ||||||
chr4:157120947
|
A | C | 1 | a0001c0001t0005g0215 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.229+285A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157120947 | ||||||
chr4:157121040
|
A | T | 1 | a0001c0001t0001g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.229+378A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121040 | ||||||
chr4:157121164
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.229+502G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121164 | ||||||
chr4:157121202
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.229+540G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121202 | ||||||
chr4:157121215
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.229+553C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121215 | ||||||
chr4:157121330
|
C | T | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229+668C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121330 | ||||||
chr4:157121456
|
A | AT | 16 | a0001c0001t0001g0061a0001c0001t0003g0019a0001c0001t0003g0028others(13): Show | 16 | HG00639.hp1 HG01168.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.229+808dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157121456 | |||||
chr4:157121456
|
A | ATT | 18 | a0001c0001t0003g0161a0001c0001t0006g0156a0001c0001t0006g0159others(15): Show | 18 | HG00544.hp2 HG01081.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.229+807_229+808dup others(2): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157121456 | |||||
chr4:157121456
|
AT | A | 34 | a0001c0001t0001g0089a0001c0001t0002g0208a0001c0001t0003g0003others(31): Show | 35 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.229+808delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157121456 | |||||
chr4:157121511
|
C | G | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-819C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121511 | ||||||
chr4:157121585
|
A | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.230-745A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121585 | ||||||
chr4:157121605
|
T | C | 23 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.230-725T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121605 | ||||||
chr4:157121703
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.230-627C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121703 | ||||||
chr4:157121704
|
G | C | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.230-626G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157121704 | ||||||
chr4:157122007
|
G | A | 7 | a0001c0001t0003g0036a0001c0001t0003g0039a0001c0001t0003g0040others(4): Show | 7 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-323G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122007 | ||||||
chr4:157122080
|
A | G | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.230-250A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122080 | ||||||
chr4:157122092
|
G | GA | 95 | a0001c0001t0001g0153a0001c0001t0002g0002a0001c0001t0002g0008others(92): Show | 105 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.230-226dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157122092 | |||||
chr4:157122092
|
GA | G | 6 | a0001c0001t0001g0148a0001c0001t0003g0043a0001c0001t0003g0044others(3): Show | 6 | HG01891.hp2 HG02074.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-226delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 157122092 | |||||
chr4:157122130
|
TG | T | 26 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(23): Show | 27 | HG01255.hp1 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.230-199delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122130 | ||||||
chr4:157122132
|
C | T | 26 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(23): Show | 27 | HG01255.hp1 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.230-198C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122132 | ||||||
chr4:157122165
|
C | T | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.230-165C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 3/9 | chr4 | 157122165 | ||||||
chr4:157122407
|
C | T | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.297+10C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122407 | ||||||
chr4:157122468
|
T | C | 34 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(31): Show | 37 | HG00408.hp1 HG00558.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.297+71T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122468 | ||||||
chr4:157122483
|
C | T | 11 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+86C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122483 | ||||||
chr4:157122486
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.297+89C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122486 | ||||||
chr4:157122902
|
G | C | 23 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+505G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122902 | ||||||
chr4:157122904
|
T | A | 1 | a0001c0001t0002g0227 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.297+507T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157122904 | ||||||
chr4:157123249
|
A | G | 23 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+852A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157123249 | ||||||
chr4:157123289
|
A | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.297+892A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157123289 | ||||||
chr4:157123651
|
G | C | 1 | a0001c0001t0002g0199 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.297+1254G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157123651 | ||||||
chr4:157123726
|
T | G | 23 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+1329T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157123726 | ||||||
chr4:157124143
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.297+1746C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124143 | ||||||
chr4:157124144
|
A | G | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.297+1747A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124144 | ||||||
chr4:157124172
|
C | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+1775C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124172 | ||||||
chr4:157124192
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.297+1795G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124192 | ||||||
chr4:157124211
|
C | T | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+1814C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124211 | ||||||
chr4:157124413
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.297+2016C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124413 | ||||||
chr4:157124470
|
C | T | 111 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0019others(108): Show | 116 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.297+2073C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124470 | ||||||
chr4:157124473
|
A | AT | 3 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0115 | 3 | NA18984.hp2 NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.297+2081dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 157124473 | |||||
chr4:157124675
|
G | A | 2 | a0001c0001t0017g0020a0001c0002t0008g0023 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.297+2278G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124675 | ||||||
chr4:157124804
|
G | A | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.297+2407G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124804 | ||||||
chr4:157124856
|
A | C | 9 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(6): Show | 10 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+2459A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124856 | ||||||
chr4:157124885
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.297+2488G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124885 | ||||||
chr4:157124900
|
T | C | 1 | a0001c0001t0002g0233 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.297+2503T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157124900 | ||||||
chr4:157125096
|
C | T | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+2699C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125096 | ||||||
chr4:157125152
|
AG | A | 7 | a0001c0001t0004g0275a0001c0001t0004g0277a0001c0001t0004g0278others(4): Show | 7 | HG00408.hp1 NA18975.hp2 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+2756delG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125152 | ||||||
chr4:157125751
|
C | G | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0003g0288others(10): Show | 13 | HG01192.hp1 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.297+3354C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125751 | ||||||
chr4:157125786
|
A | G | 1 | a0001c0001t0010g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.297+3389A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125786 | ||||||
chr4:157125814
|
G | A | 5 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0196others(2): Show | 7 | HG00597.hp2 HG02071.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+3417G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125814 | ||||||
chr4:157125830
|
C | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.297+3433C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125830 | ||||||
chr4:157125887
|
G | T | 7 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(4): Show | 7 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+3490G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125887 | ||||||
chr4:157125968
|
A | G | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.297+3571A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157125968 | ||||||
chr4:157126021
|
C | T | 1 | a0001c0002t0006g0180 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.297+3624C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126021 | ||||||
chr4:157126121
|
G | A | 43 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(40): Show | 44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.297+3724G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126121 | ||||||
chr4:157126195
|
A | G | 2 | a0001c0001t0003g0004a0001c0001t0003g0071 | 3 | HG01256.hp2 HG01258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.297+3798A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126195 | ||||||
chr4:157126544
|
T | C | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+4147T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126544 | ||||||
chr4:157126746
|
T | A | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+4349T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126746 | ||||||
chr4:157126799
|
T | G | 3 | a0001c0001t0011g0265a0001c0001t0011g0266a0001c0001t0011g0279 | 3 | NA18939.hp2 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.297+4402T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126799 | ||||||
chr4:157126802
|
C | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+4405C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126802 | ||||||
chr4:157126932
|
T | C | 1 | a0001c0001t0013g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.297+4535T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157126932 | ||||||
chr4:157127177
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.297+4780C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127177 | ||||||
chr4:157127294
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.297+4897A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127294 | ||||||
chr4:157127300
|
T | C | 2 | a0001c0001t0002g0221a0004c0006t0002g0200 | 2 | NA19066.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.297+4903T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127300 | ||||||
chr4:157127345
|
T | G | 50 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(47): Show | 51 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.297+4948T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127345 | ||||||
chr4:157127397
|
G | A | 8 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+5000G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127397 | ||||||
chr4:157127431
|
C | T | 1 | a0001c0001t0009g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.297+5034C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127431 | ||||||
chr4:157127783
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.297+5386G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127783 | ||||||
chr4:157127793
|
C | A | 3 | a0001c0001t0010g0256a0001c0001t0010g0258a0001c0001t0010g0259 | 3 | HG02647.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.297+5396C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127793 | ||||||
chr4:157127864
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.297+5467T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127864 | ||||||
chr4:157127984
|
A | T | 109 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0019others(106): Show | 114 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.297+5587A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127984 | ||||||
chr4:157127999
|
A | C | 3 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0030 | 3 | HG01168.hp2 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.297+5602A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157127999 | ||||||
chr4:157128024
|
G | A | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+5627G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128024 | ||||||
chr4:157128192
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.297+5795A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128192 | ||||||
chr4:157128506
|
A | C | 13 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(10): Show | 14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+6109A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128506 | ||||||
chr4:157128588
|
C | T | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+6191C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128588 | ||||||
chr4:157128704
|
A | C | 1 | a0001c0001t0002g0232 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.297+6307A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128704 | ||||||
chr4:157128986
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.297+6589A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157128986 | ||||||
chr4:157129119
|
G | A | 30 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(27): Show | 30 | HG00544.hp2 HG00639.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+6722G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129119 | ||||||
chr4:157129254
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.297+6857A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129254 | ||||||
chr4:157129548
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298-6921C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129548 | ||||||
chr4:157129558
|
T | G | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.298-6911T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129558 | ||||||
chr4:157129561
|
T | C | 1 | a0001c0001t0004g0282 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.298-6908T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129561 | ||||||
chr4:157129614
|
G | T | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.298-6855G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129614 | ||||||
chr4:157129751
|
G | A | 1 | a0003c0009t0009g0107 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.298-6718G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129751 | ||||||
chr4:157129754
|
CT | C | 8 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-6706delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 157129754 | |||||
chr4:157129931
|
T | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-6538T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129931 | ||||||
chr4:157129960
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.298-6509C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157129960 | ||||||
chr4:157130016
|
C | T | 2 | a0001c0001t0002g0212a0001c0001t0009g0077 | 2 | NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.298-6453C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130016 | ||||||
chr4:157130183
|
C | T | 23 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 24 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-6286C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130183 | ||||||
chr4:157130201
|
T | G | 1 | a0001c0001t0003g0071 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.298-6268T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130201 | ||||||
chr4:157130233
|
G | A | 110 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0019others(107): Show | 115 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.298-6236G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130233 | ||||||
chr4:157130519
|
A | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-5950A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130519 | ||||||
chr4:157130623
|
A | T | 30 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(27): Show | 31 | HG01255.hp1 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.298-5846A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130623 | ||||||
chr4:157130940
|
C | T | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.298-5529C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157130940 | ||||||
chr4:157131030
|
A | G | 35 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(32): Show | 36 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.298-5439A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131030 | ||||||
chr4:157131034
|
A | AT | 43 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(40): Show | 44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-5427dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 157131034 | |||||
chr4:157131071
|
A | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-5398A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131071 | ||||||
chr4:157131139
|
A | G | 6 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(3): Show | 6 | HG01515.hp1 HG02015.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-5330A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131139 | ||||||
chr4:157131162
|
C | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-5307C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131162 | ||||||
chr4:157131312
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298-5157G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131312 | ||||||
chr4:157131401
|
A | G | 43 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(40): Show | 44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-5068A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131401 | ||||||
chr4:157131429
|
G | A | 3 | a0001c0001t0003g0073a0001c0001t0013g0017a0001c0001t0013g0018 | 3 | HG02896.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.298-5040G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131429 | ||||||
chr4:157131429
|
G | C | 1 | a0001c0002t0008g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.298-5040G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131429 | ||||||
chr4:157131453
|
A | G | 8 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-5016A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131453 | ||||||
chr4:157131486
|
A | G | 30 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(27): Show | 30 | HG00544.hp2 HG00639.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.298-4983A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131486 | ||||||
chr4:157131561
|
A | G | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-4908A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131561 | ||||||
chr4:157131577
|
C | G | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-4892C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131577 | ||||||
chr4:157131962
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.298-4507T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131962 | ||||||
chr4:157131968
|
G | A | 31 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(28): Show | 32 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-4501G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157131968 | ||||||
chr4:157132062
|
G | A | 11 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-4407G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132062 | ||||||
chr4:157132069
|
T | A | 43 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(40): Show | 44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-4400T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132069 | ||||||
chr4:157132100
|
A | G | 8 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-4369A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132100 | ||||||
chr4:157132196
|
A | G | 4 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(1): Show | 4 | HG01069.hp1 HG01993.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-4273A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132196 | ||||||
chr4:157132198
|
A | G | 1 | a0001c0001t0020g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298-4271A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132198 | ||||||
chr4:157132280
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0002g0237 | 2 | HG00408.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.298-4189A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132280 | ||||||
chr4:157132334
|
T | C | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-4135T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132334 | ||||||
chr4:157132595
|
C | T | 43 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(40): Show | 44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-3874C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132595 | ||||||
chr4:157132700
|
C | A | 2 | a0001c0001t0003g0033a0001c0001t0003g0035 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.298-3769C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132700 | ||||||
chr4:157132789
|
G | A | 5 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-3680G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132789 | ||||||
chr4:157132973
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.298-3496T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157132973 | ||||||
chr4:157133006
|
T | C | 31 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(28): Show | 32 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-3463T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133006 | ||||||
chr4:157133071
|
A | C | 4 | a0001c0001t0005g0169a0001c0001t0005g0182a0001c0001t0014g0254others(1): Show | 4 | HG01255.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-3398A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133071 | ||||||
chr4:157133106
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.298-3363A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133106 | ||||||
chr4:157133183
|
A | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.298-3286A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133183 | ||||||
chr4:157133212
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.298-3257T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133212 | ||||||
chr4:157133262
|
C | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 76 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.298-3207C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133262 | ||||||
chr4:157133522
|
A | G | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-2947A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133522 | ||||||
chr4:157133534
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.298-2935C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133534 | ||||||
chr4:157133579
|
C | A | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-2890C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133579 | ||||||
chr4:157133761
|
G | A | 11 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-2708G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133761 | ||||||
chr4:157133881
|
G | C | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.298-2588G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133881 | ||||||
chr4:157133888
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0132 | 2 | HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.298-2581A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157133888 | ||||||
chr4:157134003
|
A | G | 2 | a0001c0001t0005g0169a0001c0001t0005g0182 | 2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298-2466A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134003 | ||||||
chr4:157134271
|
G | A | 31 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(28): Show | 32 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-2198G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134271 | ||||||
chr4:157134337
|
G | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-2132G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134337 | ||||||
chr4:157134458
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298-2011C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134458 | ||||||
chr4:157134860
|
G | A | 1 | a0001c0001t0014g0254 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.298-1609G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134860 | ||||||
chr4:157134886
|
GC | G | 31 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(28): Show | 32 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.298-1582delC | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157134886 | ||||||
chr4:157135070
|
G | A | 1 | a0001c0001t0022g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.298-1399G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135070 | ||||||
chr4:157135179
|
A | G | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-1290A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135179 | ||||||
chr4:157135311
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0093 | 2 | NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.298-1158G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135311 | ||||||
chr4:157135535
|
T | C | 1 | a0001c0001t0014g0254 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.298-934T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135535 | ||||||
chr4:157135697
|
A | G | 1 | a0001c0001t0013g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.298-772A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135697 | ||||||
chr4:157135889
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0118a0001c0001t0005g0216 | 3 | HG01884.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.298-580C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135889 | ||||||
chr4:157135942
|
G | A | 43 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(40): Show | 44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.298-527G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135942 | ||||||
chr4:157135996
|
C | T | 1 | a0001c0002t0008g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.298-473C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157135996 | ||||||
chr4:157136094
|
C | A | 1 | a0001c0001t0003g0033 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298-375C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157136094 | ||||||
chr4:157136447
|
C | T | 1 | a0001c0001t0013g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.298-22C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 4/9 | chr4 | 157136447 | ||||||
chr4:157137410
|
A | G | 32 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(29): Show | 33 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.610+524A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137410 | ||||||
chr4:157137418
|
A | C | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.610+532A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137418 | ||||||
chr4:157137483
|
C | CA | 12 | a0001c0001t0003g0049a0001c0001t0003g0073a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.610+608dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 157137483 | |||||
chr4:157137483
|
CA | C | 7 | a0001c0001t0003g0036a0001c0001t0003g0039a0001c0001t0003g0040others(4): Show | 7 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+608delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 157137483 | |||||
chr4:157137490
|
A | C | 1 | a0001c0002t0008g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.610+604A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137490 | ||||||
chr4:157137499
|
A | G | 1 | a0001c0001t0004g0268 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.610+613A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137499 | ||||||
chr4:157137518
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.610+632C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137518 | ||||||
chr4:157137589
|
A | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.610+703A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137589 | ||||||
chr4:157137734
|
A | G | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.610+848A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137734 | ||||||
chr4:157137754
|
A | G | 1 | a0001c0001t0022g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.610+868A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157137754 | ||||||
chr4:157138029
|
G | A | 1 | a0001c0001t0002g0223 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.611-780G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138029 | ||||||
chr4:157138082
|
T | G | 1 | a0001c0001t0003g0073 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.611-727T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138082 | ||||||
chr4:157138133
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0002g0226 | 3 | HG01070.hp2 HG01109.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.611-676G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138133 | ||||||
chr4:157138160
|
T | C | 43 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(40): Show | 44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.611-649T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138160 | ||||||
chr4:157138162
|
T | C | 43 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(40): Show | 44 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.611-647T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138162 | ||||||
chr4:157138206
|
A | G | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.611-603A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138206 | ||||||
chr4:157138470
|
G | T | 1 | a0001c0001t0003g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.611-339G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138470 | ||||||
chr4:157138743
|
A | G | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.611-66A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138743 | ||||||
chr4:157138745
|
G | T | 1 | a0001c0001t0021g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.611-64G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138745 | ||||||
chr4:157138795
|
G | A | 6 | a0001c0001t0005g0252a0001c0001t0007g0218a0001c0001t0007g0219others(3): Show | 6 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.611-14G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 6/9 | chr4 | 157138795 | ||||||
chr4:157139121
|
GT | G | 42 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(39): Show | 43 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.751+178delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 157139121 | |||||
chr4:157139147
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.751+198A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139147 | ||||||
chr4:157139235
|
C | T | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.751+286C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139235 | ||||||
chr4:157139528
|
A | T | 2 | a0001c0002t0008g0157a0001c0002t0008g0163 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.751+579A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139528 | ||||||
chr4:157139650
|
T | A | 32 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(29): Show | 33 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.751+701T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139650 | ||||||
chr4:157139743
|
C | T | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.751+794C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139743 | ||||||
chr4:157139761
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.751+812A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139761 | ||||||
chr4:157139981
|
G | A | 4 | a0001c0001t0002g0204a0001c0001t0002g0207a0001c0001t0002g0246others(1): Show | 4 | NA18980.hp2 NA19054.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.751+1032G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157139981 | ||||||
chr4:157140085
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.751+1136A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140085 | ||||||
chr4:157140251
|
A | G | 44 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(41): Show | 45 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.751+1302A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140251 | ||||||
chr4:157140633
|
A | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0255 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.751+1684A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140633 | ||||||
chr4:157140698
|
T | A | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.751+1749T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140698 | ||||||
chr4:157140712
|
G | A | 32 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(29): Show | 33 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.751+1763G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140712 | ||||||
chr4:157140724
|
T | C | 1 | a0001c0001t0021g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.751+1775T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140724 | ||||||
chr4:157140931
|
G | A | 42 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(39): Show | 43 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.751+1982G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140931 | ||||||
chr4:157140956
|
G | T | 3 | a0001c0001t0003g0073a0001c0001t0013g0017a0001c0001t0013g0018 | 3 | HG02896.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.751+2007G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140956 | ||||||
chr4:157140970
|
A | G | 1 | a0001c0001t0022g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751+2021A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157140970 | ||||||
chr4:157141069
|
T | G | 1 | a0001c0001t0003g0255 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.751+2120T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141069 | ||||||
chr4:157141088
|
G | T | 3 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0008t0024g0287 | 3 | HG02145.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.751+2139G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141088 | ||||||
chr4:157141255
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.751+2306C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141255 | ||||||
chr4:157141537
|
G | C | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.752-2270G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141537 | ||||||
chr4:157141862
|
T | C | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.752-1945T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141862 | ||||||
chr4:157141938
|
T | C | 9 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0062others(6): Show | 9 | HG00733.hp2 HG01070.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.752-1869T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141938 | ||||||
chr4:157141951
|
G | A | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.752-1856G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157141951 | ||||||
chr4:157142067
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0025g0121 | 2 | HG01109.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.752-1740A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157142067 | ||||||
chr4:157142196
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.752-1611A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157142196 | ||||||
chr4:157142218
|
G | A | 9 | a0001c0001t0005g0252a0001c0001t0007g0193a0001c0001t0007g0218others(6): Show | 9 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.752-1589G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157142218 | ||||||
chr4:157142802
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.752-1005A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157142802 | ||||||
chr4:157143067
|
A | T | 42 | a0001c0001t0003g0004a0001c0001t0003g0019a0001c0001t0003g0027others(39): Show | 43 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.752-740A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143067 | ||||||
chr4:157143332
|
T | G | 180 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(177): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.752-475T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143332 | ||||||
chr4:157143444
|
G | C | 1 | a0001c0001t0003g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.752-363G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143444 | ||||||
chr4:157143508
|
A | G | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.752-299A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143508 | ||||||
chr4:157143634
|
A | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0062a0001c0001t0001g0063 | 3 | HG01070.hp1 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.752-173A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 7/9 | chr4 | 157143634 | ||||||
chr4:157143963
|
A | T | 8 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.904+4A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157143963 | ||||||
chr4:157144236
|
G | A | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.904+277G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144236 | ||||||
chr4:157144351
|
C | A | 111 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0019others(108): Show | 116 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.904+392C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144351 | ||||||
chr4:157144387
|
A | G | 288 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.904+428A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144387 | ||||||
chr4:157144438
|
C | G | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0252others(9): Show | 12 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.904+479C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144438 | ||||||
chr4:157144569
|
C | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0264others(22): Show | 28 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.904+610C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144569 | ||||||
chr4:157144797
|
C | T | 1 | a0001c0001t0012g0092 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.904+838C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144797 | ||||||
chr4:157144803
|
A | T | 1 | a0001c0001t0010g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.904+844A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144803 | ||||||
chr4:157144828
|
A | C | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.904+869A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144828 | ||||||
chr4:157144936
|
T | C | 177 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(174): Show | 189 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.904+977T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157144936 | ||||||
chr4:157145073
|
T | C | 3 | a0001c0001t0003g0046a0001c0002t0008g0023a0001c0002t0008g0024 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.904+1114T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145073 | ||||||
chr4:157145228
|
C | A | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.904+1269C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145228 | ||||||
chr4:157145316
|
A | T | 1 | a0001c0002t0012g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.904+1357A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145316 | ||||||
chr4:157145432
|
G | A | 66 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(63): Show | 73 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.904+1473G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145432 | ||||||
chr4:157145766
|
C | T | 4 | a0001c0001t0010g0256a0001c0001t0010g0258a0001c0001t0010g0259others(1): Show | 4 | HG02647.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+1807C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157145766 | ||||||
chr4:157146024
|
C | CT | 7 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(4): Show | 7 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.904+2077dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 157146024 | |||||
chr4:157146040
|
G | A | 1 | a0001c0001t0013g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.904+2081G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146040 | ||||||
chr4:157146144
|
A | G | 14 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(11): Show | 14 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.904+2185A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146144 | ||||||
chr4:157146160
|
G | C | 14 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(11): Show | 14 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.904+2201G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146160 | ||||||
chr4:157146236
|
C | T | 1 | a0001c0002t0006g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.904+2277C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146236 | ||||||
chr4:157146239
|
A | G | 1 | a0001c0002t0006g0189 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.904+2280A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146239 | ||||||
chr4:157146428
|
C | T | 66 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(63): Show | 73 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.904+2469C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146428 | ||||||
chr4:157146558
|
C | G | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.904+2599C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146558 | ||||||
chr4:157146558
|
C | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+2599C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146558 | ||||||
chr4:157146656
|
C | CAAAAATG others(310): Show |
3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+2713_904+2714i others(319): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 157146656 | |||||
chr4:157146834
|
C | CA | 8 | a0001c0001t0001g0122a0001c0001t0003g0036a0001c0001t0003g0039others(5): Show | 8 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+2886dupA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 157146834 | |||||
chr4:157146899
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.904+2940G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146899 | ||||||
chr4:157146985
|
G | A | 3 | a0001c0001t0011g0265a0001c0001t0011g0266a0001c0001t0011g0279 | 3 | NA18939.hp2 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.904+3026G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157146985 | ||||||
chr4:157147159
|
C | T | 34 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(31): Show | 35 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.904+3200C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147159 | ||||||
chr4:157147160
|
T | A | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.904+3201T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147160 | ||||||
chr4:157147298
|
A | T | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.904+3339A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147298 | ||||||
chr4:157147347
|
T | C | 1 | a0001c0001t0004g0270 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.904+3388T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147347 | ||||||
chr4:157147362
|
T | A | 1 | a0001c0001t0020g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.904+3403T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147362 | ||||||
chr4:157147406
|
A | G | 70 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(67): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.904+3447A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147406 | ||||||
chr4:157147465
|
GA | G | 34 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(31): Show | 35 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.904+3507delA | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147465 | ||||||
chr4:157147697
|
G | A | 5 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.904+3738G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147697 | ||||||
chr4:157147859
|
C | G | 175 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(172): Show | 187 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.904+3900C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147859 | ||||||
chr4:157147890
|
C | T | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.904+3931C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147890 | ||||||
chr4:157147906
|
G | T | 1 | a0001c0001t0006g0262 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.904+3947G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147906 | ||||||
chr4:157147933
|
G | A | 3 | a0001c0001t0003g0073a0001c0001t0013g0017a0001c0001t0013g0018 | 3 | HG02896.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.904+3974G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157147933 | ||||||
chr4:157148033
|
G | C | 1 | a0001c0001t0021g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904+4074G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148033 | ||||||
chr4:157148213
|
T | C | 12 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(9): Show | 12 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.904+4254T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148213 | ||||||
chr4:157148239
|
A | G | 5 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.904+4280A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148239 | ||||||
chr4:157148398
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG00544.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.905-4320C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148398 | ||||||
chr4:157148479
|
C | T | 178 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(175): Show | 190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.905-4239C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148479 | ||||||
chr4:157148815
|
T | TTTG | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-3898_905-3896d others(5): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 157148815 | |||||
chr4:157148906
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.905-3812G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148906 | ||||||
chr4:157148944
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905-3774C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157148944 | ||||||
chr4:157149102
|
A | G | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-3616A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149102 | ||||||
chr4:157149193
|
G | A | 1 | a0001c0001t0005g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.905-3525G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149193 | ||||||
chr4:157149337
|
A | G | 2 | a0001c0002t0008g0023a0001c0002t0008g0024 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.905-3381A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149337 | ||||||
chr4:157149413
|
G | A | 2 | a0001c0001t0002g0011a0001c0001t0003g0026 | 3 | HG02572.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.905-3305G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149413 | ||||||
chr4:157149478
|
T | C | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905-3240T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149478 | ||||||
chr4:157149921
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.905-2797A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149921 | ||||||
chr4:157149959
|
G | A | 70 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(67): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.905-2759G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157149959 | ||||||
chr4:157150017
|
T | C | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-2701T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150017 | ||||||
chr4:157150194
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.905-2524G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150194 | ||||||
chr4:157150246
|
C | A | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-2472C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150246 | ||||||
chr4:157150308
|
G | A | 3 | a0001c0001t0002g0231a0001c0001t0015g0187a0001c0001t0015g0240 | 3 | HG01952.hp2 HG02293.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.905-2410G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150308 | ||||||
chr4:157150518
|
A | C | 1 | a0001c0001t0022g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905-2200A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150518 | ||||||
chr4:157150530
|
C | A | 82 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(79): Show | 89 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.905-2188C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150530 | ||||||
chr4:157150619
|
G | A | 70 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(67): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.905-2099G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150619 | ||||||
chr4:157150730
|
G | A | 1 | a0001c0001t0020g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.905-1988G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150730 | ||||||
chr4:157150799
|
G | C | 46 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 47 | HG01081.hp2 HG01192.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.905-1919G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150799 | ||||||
chr4:157150847
|
G | T | 33 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(30): Show | 34 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.905-1871G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150847 | ||||||
chr4:157150864
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.905-1854T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150864 | ||||||
chr4:157150921
|
C | A | 1 | a0001c0001t0003g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.905-1797C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150921 | ||||||
chr4:157150922
|
C | A | 1 | a0001c0001t0003g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.905-1796C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150922 | ||||||
chr4:157150923
|
A | C | 15 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(12): Show | 15 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.905-1795A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157150923 | ||||||
chr4:157151019
|
C | A | 1 | a0001c0001t0001g0155 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.905-1699C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151019 | ||||||
chr4:157151255
|
T | C | 25 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(22): Show | 26 | HG01081.hp2 HG01884.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.905-1463T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151255 | ||||||
chr4:157151286
|
A | G | 27 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(24): Show | 28 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.905-1432A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151286 | ||||||
chr4:157151379
|
T | G | 1 | a0001c0002t0008g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.905-1339T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151379 | ||||||
chr4:157151586
|
C | A | 33 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(30): Show | 34 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.905-1132C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151586 | ||||||
chr4:157151973
|
C | G | 7 | a0001c0001t0003g0036a0001c0001t0003g0039a0001c0001t0003g0040others(4): Show | 7 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.905-745C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157151973 | ||||||
chr4:157152048
|
A | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0132 | 3 | HG01175.hp1 HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.905-670A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157152048 | ||||||
chr4:157152256
|
A | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0129 | 2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.905-462A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157152256 | ||||||
chr4:157152452
|
C | A | 2 | a0001c0001t0010g0258a0001c0001t0010g0259 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.905-266C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157152452 | ||||||
chr4:157152558
|
G | A | 2 | a0001c0001t0010g0258a0001c0001t0010g0259 | 2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.905-160G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 8/9 | chr4 | 157152558 | ||||||
chr4:157153074
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1197+64C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153074 | ||||||
chr4:157153153
|
A | G | 1 | a0001c0001t0002g0247 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1197+143A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153153 | ||||||
chr4:157153206
|
G | A | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1197+196G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153206 | ||||||
chr4:157153351
|
T | C | 27 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(24): Show | 28 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1197+341T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153351 | ||||||
chr4:157153512
|
T | G | 1 | a0001c0003t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1197+502T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153512 | ||||||
chr4:157153606
|
C | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+596C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153606 | ||||||
chr4:157153619
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1197+609C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153619 | ||||||
chr4:157153642
|
A | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+632A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153642 | ||||||
chr4:157153664
|
T | C | 46 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(43): Show | 47 | HG01081.hp2 HG01192.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.1197+654T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153664 | ||||||
chr4:157153735
|
C | T | 27 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(24): Show | 28 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1197+725C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153735 | ||||||
chr4:157153790
|
G | A | 27 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(24): Show | 28 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1197+780G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153790 | ||||||
chr4:157153851
|
C | T | 1 | a0001c0001t0018g0235 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1197+841C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153851 | ||||||
chr4:157153921
|
G | A | 1 | a0001c0001t0009g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1197+911G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157153921 | ||||||
chr4:157154113
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+1103G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154113 | ||||||
chr4:157154423
|
C | CT | 49 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0117others(46): Show | 50 | HG00280.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1197+1434dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157154423 | |||||
chr4:157154423
|
CT | C | 10 | a0001c0001t0001g0109a0001c0001t0003g0004a0001c0001t0003g0037others(7): Show | 11 | HG00733.hp1 HG00738.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+1434delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157154423 | |||||
chr4:157154423
|
CTT | C | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0243others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+1433_1197+143 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157154423 | |||||
chr4:157154479
|
G | A | 3 | a0001c0002t0006g0179a0001c0002t0006g0180a0001c0002t0006g0181 | 3 | HG02015.hp1 HG02080.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1197+1469G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154479 | ||||||
chr4:157154505
|
G | A | 8 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1197+1495G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154505 | ||||||
chr4:157154506
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1197+1496C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154506 | ||||||
chr4:157154552
|
C | T | 4 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(1): Show | 4 | HG01255.hp1 HG02145.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+1542C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154552 | ||||||
chr4:157154578
|
C | A | 1 | a0001c0001t0005g0249 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1197+1568C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154578 | ||||||
chr4:157154586
|
T | G | 1 | a0001c0001t0003g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1197+1576T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154586 | ||||||
chr4:157154625
|
T | C | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1197+1615T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154625 | ||||||
chr4:157154642
|
G | C | 13 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(10): Show | 13 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1197+1632G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154642 | ||||||
chr4:157154867
|
C | T | 1 | a0001c0001t0007g0243 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1197+1857C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154867 | ||||||
chr4:157154911
|
A | G | 4 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(1): Show | 4 | HG01255.hp1 HG02145.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+1901A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154911 | ||||||
chr4:157154915
|
G | A | 33 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(30): Show | 34 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.1197+1905G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154915 | ||||||
chr4:157154960
|
A | G | 3 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0070 | 3 | HG02074.hp1 HG02132.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1197+1950A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157154960 | ||||||
chr4:157155144
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1197+2134T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155144 | ||||||
chr4:157155199
|
A | C | 5 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0243others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+2189A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155199 | ||||||
chr4:157155221
|
T | G | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1197+2211T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155221 | ||||||
chr4:157155272
|
G | T | 1 | a0001c0001t0022g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1197+2262G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155272 | ||||||
chr4:157155431
|
C | T | 14 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+2421C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155431 | ||||||
chr4:157155535
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1197+2525T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155535 | ||||||
chr4:157155573
|
A | G | 70 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(67): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1197+2563A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155573 | ||||||
chr4:157155675
|
G | A | 1 | a0001c0001t0005g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1197+2665G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155675 | ||||||
chr4:157155686
|
C | T | 1 | a0001c0001t0004g0263 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1197+2676C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155686 | ||||||
chr4:157155690
|
T | C | 13 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(10): Show | 14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1197+2680T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155690 | ||||||
chr4:157155775
|
C | A | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+2765C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155775 | ||||||
chr4:157155784
|
G | C | 14 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+2774G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157155784 | ||||||
chr4:157156204
|
C | T | 1 | a0001c0001t0007g0251 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1197+3194C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156204 | ||||||
chr4:157156394
|
T | C | 13 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(10): Show | 14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1197+3384T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156394 | ||||||
chr4:157156406
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1197+3396C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156406 | ||||||
chr4:157156413
|
C | T | 1 | a0001c0001t0007g0193 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1197+3403C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156413 | ||||||
chr4:157156414
|
G | A | 12 | a0001c0001t0003g0019a0001c0001t0003g0027a0001c0001t0003g0028others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+3404G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156414 | ||||||
chr4:157156526
|
T | A | 1 | a0001c0001t0009g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1197+3516T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156526 | ||||||
chr4:157156632
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+3622G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156632 | ||||||
chr4:157156718
|
T | C | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+3708T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157156718 | ||||||
chr4:157157044
|
A | G | 289 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(286): Show | 305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1197+4034A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157044 | ||||||
chr4:157157056
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1197+4046A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157056 | ||||||
chr4:157157093
|
G | A | 1 | a0001c0002t0012g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1197+4083G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157093 | ||||||
chr4:157157109
|
C | A | 33 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(30): Show | 34 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.1197+4099C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157109 | ||||||
chr4:157157224
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1197+4214A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157224 | ||||||
chr4:157157327
|
G | A | 2 | a0001c0001t0003g0037a0001c0001t0016g0176 | 2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1197+4317G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157327 | ||||||
chr4:157157336
|
C | T | 4 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(1): Show | 4 | HG01255.hp1 HG02145.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+4326C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157336 | ||||||
chr4:157157465
|
G | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+4455G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157465 | ||||||
chr4:157157488
|
C | T | 5 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197+4478C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157488 | ||||||
chr4:157157497
|
C | A | 4 | a0001c0001t0003g0073a0001c0001t0013g0017a0001c0001t0013g0018others(1): Show | 4 | HG02896.hp1 HG03195.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+4487C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157497 | ||||||
chr4:157157647
|
G | A | 45 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(42): Show | 46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+4637G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157647 | ||||||
chr4:157157717
|
A | T | 6 | a0001c0001t0005g0169a0001c0003t0001g0058a0001c0003t0001g0087others(3): Show | 6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1197+4707A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157717 | ||||||
chr4:157157739
|
T | C | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+4729T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157157739 | ||||||
chr4:157158056
|
T | G | 178 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(175): Show | 190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1197+5046T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158056 | ||||||
chr4:157158112
|
T | C | 7 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(4): Show | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+5102T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158112 | ||||||
chr4:157158173
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1197+5163T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158173 | ||||||
chr4:157158217
|
G | C | 1 | a0001c0001t0004g0277 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1197+5207G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158217 | ||||||
chr4:157158382
|
C | T | 4 | a0001c0002t0006g0179a0001c0002t0006g0180a0001c0002t0006g0181others(1): Show | 4 | HG00544.hp2 HG02015.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+5372C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158382 | ||||||
chr4:157158456
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1197+5446T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158456 | ||||||
chr4:157158618
|
G | C | 7 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(4): Show | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+5608G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158618 | ||||||
chr4:157158790
|
G | T | 12 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(9): Show | 12 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+5780G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158790 | ||||||
chr4:157158809
|
A | T | 1 | a0001c0001t0005g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1197+5799A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157158809 | ||||||
chr4:157158888
|
T | TG | 57 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(54): Show | 58 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.1197+5881dupG | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157158888 | |||||
chr4:157159050
|
C | G | 1 | a0001c0002t0008g0157 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1197+6040C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159050 | ||||||
chr4:157159063
|
A | T | 45 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(42): Show | 46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+6053A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159063 | ||||||
chr4:157159110
|
G | A | 7 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(4): Show | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+6100G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159110 | ||||||
chr4:157159261
|
A | G | 5 | a0001c0001t0002g0184a0001c0001t0002g0190a0001c0001t0002g0191others(2): Show | 5 | HG01123.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+6251A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159261 | ||||||
chr4:157159375
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1197+6365A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159375 | ||||||
chr4:157159399
|
T | G | 2 | a0001c0002t0008g0157a0001c0002t0008g0163 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1197+6389T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159399 | ||||||
chr4:157159529
|
G | C | 1 | a0001c0001t0020g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1197+6519G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159529 | ||||||
chr4:157159530
|
T | G | 7 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(4): Show | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+6520T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159530 | ||||||
chr4:157159553
|
A | G | 1 | a0001c0001t0013g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1197+6543A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159553 | ||||||
chr4:157159592
|
A | G | 1 | a0001c0001t0013g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1197+6582A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159592 | ||||||
chr4:157159622
|
G | T | 11 | a0001c0001t0003g0046a0001c0001t0003g0049a0001c0001t0003g0161others(8): Show | 11 | HG01081.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+6612G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159622 | ||||||
chr4:157159624
|
A | C | 11 | a0001c0001t0003g0046a0001c0001t0003g0049a0001c0001t0003g0161others(8): Show | 11 | HG01081.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+6614A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159624 | ||||||
chr4:157159624
|
A | G | 6 | a0001c0001t0002g0008a0001c0001t0002g0185a0001c0001t0004g0264others(3): Show | 7 | HG00558.hp2 HG02040.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+6614A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159624 | ||||||
chr4:157159628
|
G | A | 11 | a0001c0001t0003g0046a0001c0001t0003g0049a0001c0001t0003g0161others(8): Show | 11 | HG01081.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+6618G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159628 | ||||||
chr4:157159694
|
T | C | 1 | a0001c0002t0012g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1197+6684T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159694 | ||||||
chr4:157159699
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+6689G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159699 | ||||||
chr4:157159763
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1197+6753A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159763 | ||||||
chr4:157159772
|
C | T | 2 | a0001c0002t0008g0157a0001c0002t0008g0163 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1197+6762C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159772 | ||||||
chr4:157159816
|
A | C | 1 | a0001c0002t0008g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1197+6806A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159816 | ||||||
chr4:157159860
|
G | A | 4 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(1): Show | 4 | HG01255.hp1 HG02145.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+6850G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159860 | ||||||
chr4:157159953
|
C | T | 14 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+6943C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157159953 | ||||||
chr4:157160043
|
C | T | 14 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+7033C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160043 | ||||||
chr4:157160046
|
T | C | 7 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+7036T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160046 | ||||||
chr4:157160077
|
G | A | 2 | a0001c0002t0008g0023a0001c0002t0008g0024 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1197+7067G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160077 | ||||||
chr4:157160092
|
T | G | 1 | a0001c0001t0002g0212 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1197+7082T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160092 | ||||||
chr4:157160108
|
A | T | 1 | a0001c0001t0002g0212 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1197+7098A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160108 | ||||||
chr4:157160163
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1197+7153C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160163 | ||||||
chr4:157160170
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0144 | 2 | HG01123.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1197+7160G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160170 | ||||||
chr4:157160171
|
G | T | 1 | a0001c0001t0003g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1197+7161G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160171 | ||||||
chr4:157160173
|
G | A | 5 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197+7163G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160173 | ||||||
chr4:157160258
|
A | AT | 45 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(42): Show | 46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+7255dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157160258 | |||||
chr4:157160290
|
A | T | 6 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(3): Show | 6 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+7280A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160290 | ||||||
chr4:157160371
|
C | A | 7 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(4): Show | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1197+7361C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160371 | ||||||
chr4:157160415
|
C | T | 165 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(162): Show | 176 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1197+7405C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160415 | ||||||
chr4:157160530
|
T | G | 9 | a0001c0001t0003g0049a0001c0001t0003g0161a0001c0001t0006g0156others(6): Show | 9 | HG01081.hp2 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1197+7520T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160530 | ||||||
chr4:157160601
|
C | T | 178 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(175): Show | 190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1197+7591C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160601 | ||||||
chr4:157160610
|
A | G | 6 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(3): Show | 6 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+7600A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160610 | ||||||
chr4:157160623
|
T | G | 45 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(42): Show | 46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+7613T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160623 | ||||||
chr4:157160638
|
G | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1197+7628G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160638 | ||||||
chr4:157160675
|
G | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+7665G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160675 | ||||||
chr4:157160716
|
T | C | 1 | a0001c0001t0013g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1197+7706T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160716 | ||||||
chr4:157160772
|
T | G | 1 | a0001c0001t0003g0073 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1197+7762T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160772 | ||||||
chr4:157160776
|
T | C | 45 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(42): Show | 46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+7766T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160776 | ||||||
chr4:157160892
|
T | A | 1 | a0001c0001t0012g0092 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1197+7882T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160892 | ||||||
chr4:157160904
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1197+7894G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157160904 | ||||||
chr4:157161022
|
C | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+8012C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161022 | ||||||
chr4:157161043
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1197+8033T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161043 | ||||||
chr4:157161223
|
T | A | 45 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(42): Show | 46 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1197+8213T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161223 | ||||||
chr4:157161284
|
A | G | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1197+8274A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161284 | ||||||
chr4:157161301
|
C | A | 1 | a0001c0001t0013g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1197+8291C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161301 | ||||||
chr4:157161351
|
G | A | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+8341G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161351 | ||||||
chr4:157161370
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1197+8360A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161370 | ||||||
chr4:157161535
|
A | C | 1 | a0001c0001t0002g0197 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1197+8525A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161535 | ||||||
chr4:157161566
|
A | T | 1 | a0001c0001t0023g0273 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1197+8556A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161566 | ||||||
chr4:157161699
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1197+8689C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161699 | ||||||
chr4:157161711
|
G | A | 14 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+8701G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161711 | ||||||
chr4:157161718
|
T | C | 70 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(67): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1197+8708T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161718 | ||||||
chr4:157161727
|
T | A | 7 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(4): Show | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198-8705T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157161727 | ||||||
chr4:157162123
|
C | T | 14 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1198-8309C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162123 | ||||||
chr4:157162168
|
G | T | 3 | a0001c0001t0004g0267a0001c0001t0004g0268a0001c0001t0004g0269 | 3 | NA18967.hp2 NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1198-8264G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162168 | ||||||
chr4:157162217
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1198-8215C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162217 | ||||||
chr4:157162234
|
C | A | 164 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(161): Show | 175 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1198-8198C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162234 | ||||||
chr4:157162280
|
C | A | 5 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-8152C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162280 | ||||||
chr4:157162312
|
A | C | 1 | a0003c0009t0009g0107 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1198-8120A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162312 | ||||||
chr4:157162444
|
C | A | 13 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(10): Show | 14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1198-7988C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162444 | ||||||
chr4:157162460
|
T | C | 1 | a0001c0001t0005g0210 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1198-7972T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162460 | ||||||
chr4:157162511
|
C | T | 23 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0267others(20): Show | 26 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-7921C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162511 | ||||||
chr4:157162518
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1198-7914G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162518 | ||||||
chr4:157162580
|
T | C | 6 | a0001c0001t0005g0169a0001c0003t0001g0058a0001c0003t0001g0087others(3): Show | 6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198-7852T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162580 | ||||||
chr4:157162603
|
C | A | 1 | a0001c0001t0003g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1198-7829C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162603 | ||||||
chr4:157162667
|
A | G | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1198-7765A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162667 | ||||||
chr4:157162682
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1198-7750A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162682 | ||||||
chr4:157162684
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1198-7748C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162684 | ||||||
chr4:157162701
|
C | T | 8 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(5): Show | 8 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.1198-7731C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162701 | ||||||
chr4:157162718
|
C | T | 2 | a0001c0001t0002g0203a0001c0001t0002g0230 | 2 | HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1198-7714C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162718 | ||||||
chr4:157162724
|
T | C | 70 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(67): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1198-7708T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162724 | ||||||
chr4:157162729
|
G | A | 1 | a0001c0001t0020g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1198-7703G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162729 | ||||||
chr4:157162743
|
C | G | 23 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0267others(20): Show | 26 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-7689C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157162743 | ||||||
chr4:157163024
|
C | T | 12 | a0001c0002t0006g0177a0001c0002t0006g0178a0001c0002t0006g0179others(9): Show | 12 | HG00544.hp2 HG01515.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-7408C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163024 | ||||||
chr4:157163137
|
C | T | 5 | a0001c0001t0001g0072a0001c0001t0002g0184a0001c0001t0002g0190others(2): Show | 5 | HG01123.hp2 HG01258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-7295C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163137 | ||||||
chr4:157163178
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1198-7254G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163178 | ||||||
chr4:157163212
|
C | G | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-7220C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163212 | ||||||
chr4:157163310
|
C | T | 2 | a0001c0001t0004g0267a0001c0001t0004g0268 | 2 | NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1198-7122C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163310 | ||||||
chr4:157163311
|
A | G | 178 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(175): Show | 190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1198-7121A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163311 | ||||||
chr4:157163322
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1198-7110C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163322 | ||||||
chr4:157163323
|
G | A | 1 | a0001c0001t0002g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1198-7109G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163323 | ||||||
chr4:157163391
|
C | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-7041C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163391 | ||||||
chr4:157163425
|
C | G | 1 | a0001c0002t0008g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1198-7007C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163425 | ||||||
chr4:157163436
|
T | C | 288 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1198-6996T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163436 | ||||||
chr4:157163437
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1198-6995G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163437 | ||||||
chr4:157163521
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0005g0214 | 2 | NA18956.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1198-6911C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163521 | ||||||
chr4:157163522
|
G | A | 23 | a0001c0001t0004g0001a0001c0001t0004g0263a0001c0001t0004g0267others(20): Show | 26 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-6910G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163522 | ||||||
chr4:157163787
|
C | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-6645C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163787 | ||||||
chr4:157163829
|
A | AGT | 4 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0099others(1): Show | 4 | HG00741.hp1 HG02080.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-6580_1198-657 others(6): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGT | 7 | a0001c0001t0003g0019a0001c0001t0003g0031a0001c0001t0007g0218others(4): Show | 7 | HG02145.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1198-6584_1198-657 others(10): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(1): Show |
11 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1198-6586_1198-657 others(12): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(3): Show |
15 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0004g0001others(12): Show | 18 | HG00544.hp2 HG00558.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1198-6588_1198-657 others(14): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(5): Show |
26 | a0001c0001t0004g0263a0001c0001t0004g0268a0001c0001t0004g0269others(23): Show | 26 | HG00408.hp1 HG02015.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-6590_1198-657 others(16): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(7): Show |
2 | a0001c0001t0003g0046a0001c0002t0008g0023 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1198-6592_1198-657 others(18): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(9): Show |
12 | a0001c0001t0003g0040a0001c0001t0003g0042a0001c0001t0003g0049others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-6594_1198-657 others(20): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(11): Show |
13 | a0001c0001t0003g0021a0001c0001t0003g0036a0001c0001t0003g0039others(10): Show | 13 | HG01255.hp1 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1198-6596_1198-657 others(22): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(13): Show |
2 | a0001c0001t0003g0003a0001c0001t0003g0022 | 3 | HG01884.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1198-6598_1198-657 others(24): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(15): Show |
3 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0183 | 3 | HG02615.hp2 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1198-6600_1198-657 others(26): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163829
|
A | AGTGTGTG others(17): Show |
3 | a0001c0001t0003g0073a0001c0001t0003g0174a0001c0001t0016g0176 | 3 | HG02486.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1198-6602_1198-657 others(28): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157163829 | |||||
chr4:157163874
|
T | C | 1 | a0001c0001t0017g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1198-6558T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163874 | ||||||
chr4:157163880
|
T | C | 2 | a0001c0001t0004g0001a0001c0001t0004g0276 | 5 | HG00558.hp1 NA18964.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-6552T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157163880 | ||||||
chr4:157164007
|
T | C | 5 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-6425T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164007 | ||||||
chr4:157164025
|
G | T | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-6407G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164025 | ||||||
chr4:157164120
|
G | A | 1 | a0001c0008t0024g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1198-6312G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164120 | ||||||
chr4:157164144
|
A | AT | 32 | a0001c0001t0001g0109a0001c0001t0001g0153a0001c0001t0003g0026others(29): Show | 35 | HG00408.hp1 HG00558.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.1198-6276dupT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157164144 | |||||
chr4:157164243
|
G | T | 1 | a0001c0001t0002g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1198-6189G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164243 | ||||||
chr4:157164394
|
A | G | 1 | a0001c0001t0013g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1198-6038A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164394 | ||||||
chr4:157164546
|
C | T | 13 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(10): Show | 14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1198-5886C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164546 | ||||||
chr4:157164923
|
T | C | 13 | a0001c0001t0003g0004a0001c0001t0003g0037a0001c0001t0003g0043others(10): Show | 14 | HG00733.hp1 HG00738.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1198-5509T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164923 | ||||||
chr4:157164967
|
A | G | 2 | a0001c0001t0003g0004a0001c0001t0003g0071 | 3 | HG01256.hp2 HG01258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1198-5465A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157164967 | ||||||
chr4:157165023
|
C | T | 5 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-5409C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165023 | ||||||
chr4:157165311
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1198-5121G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165311 | ||||||
chr4:157165447
|
A | G | 3 | a0001c0002t0006g0179a0001c0002t0006g0180a0001c0002t0006g0181 | 3 | HG02015.hp1 HG02080.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1198-4985A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165447 | ||||||
chr4:157165671
|
C | G | 20 | a0001c0001t0003g0161a0001c0001t0006g0156a0001c0001t0006g0159others(17): Show | 20 | HG00544.hp2 HG01081.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.1198-4761C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165671 | ||||||
chr4:157165888
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1198-4544C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165888 | ||||||
chr4:157165997
|
G | A | 2 | a0001c0001t0003g0047a0001c0001t0003g0255 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1198-4435G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157165997 | ||||||
chr4:157166036
|
A | G | 1 | a0001c0001t0002g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1198-4396A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166036 | ||||||
chr4:157166094
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0152 | 3 | HG00280.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1198-4338G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166094 | ||||||
chr4:157166101
|
G | T | 1 | a0001c0001t0002g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1198-4331G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166101 | ||||||
chr4:157166133
|
GT | G | 94 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(91): Show | 98 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1198-4292delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157166133 | |||||
chr4:157166172
|
A | G | 2 | a0001c0002t0008g0023a0001c0002t0008g0024 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1198-4260A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166172 | ||||||
chr4:157166420
|
G | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0057 | 2 | NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1198-4012G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166420 | ||||||
chr4:157166483
|
A | T | 1 | a0001c0001t0003g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1198-3949A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166483 | ||||||
chr4:157166486
|
G | C | 3 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022 | 4 | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1198-3946G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166486 | ||||||
chr4:157166521
|
G | A | 70 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(67): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1198-3911G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166521 | ||||||
chr4:157166569
|
A | G | 12 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0005g0182others(9): Show | 12 | HG01192.hp1 HG01255.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1198-3863A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166569 | ||||||
chr4:157166613
|
A | G | 49 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(46): Show | 50 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.1198-3819A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166613 | ||||||
chr4:157166632
|
C | T | 1 | a0001c0001t0013g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1198-3800C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166632 | ||||||
chr4:157166691
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1198-3741C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166691 | ||||||
chr4:157166955
|
G | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0149others(2): Show | 6 | HG02080.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1198-3477G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157166955 | ||||||
chr4:157167220
|
C | T | 36 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(33): Show | 37 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1198-3212C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167220 | ||||||
chr4:157167281
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1198-3151T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167281 | ||||||
chr4:157167312
|
A | G | 36 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0021others(33): Show | 37 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1198-3120A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167312 | ||||||
chr4:157167893
|
A | T | 2 | a0001c0001t0002g0197a0001c0001t0002g0229 | 2 | NA18971.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1198-2539A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167893 | ||||||
chr4:157167953
|
G | A | 7 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(4): Show | 7 | HG01192.hp1 HG01981.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198-2479G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157167953 | ||||||
chr4:157168016
|
C | G | 7 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0173others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198-2416C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168016 | ||||||
chr4:157168051
|
G | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1198-2381G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168051 | ||||||
chr4:157168115
|
A | ATTT | 8 | a0001c0001t0007g0193a0001c0001t0007g0218a0001c0001t0007g0219others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1198-2306_1198-230 others(7): Show |
GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157168115 | |||||
chr4:157168115
|
AT | A | 140 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0096others(137): Show | 151 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1198-2304delT | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 157168115 | |||||
chr4:157168141
|
G | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0255 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1198-2291G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168141 | ||||||
chr4:157168266
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0057 | 2 | NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1198-2166T>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168266 | ||||||
chr4:157168375
|
A | G | 10 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0007g0193others(7): Show | 10 | HG01192.hp1 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1198-2057A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168375 | ||||||
chr4:157168434
|
C | T | 24 | a0001c0001t0001g0148a0001c0001t0006g0156a0001c0001t0006g0159others(21): Show | 24 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1198-1998C>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168434 | ||||||
chr4:157168497
|
A | T | 10 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0007g0193others(7): Show | 10 | HG01192.hp1 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1198-1935A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168497 | ||||||
chr4:157168508
|
G | A | 26 | a0001c0001t0001g0148a0001c0001t0005g0182a0001c0001t0006g0156others(23): Show | 26 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1198-1924G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168508 | ||||||
chr4:157168560
|
C | G | 24 | a0001c0001t0001g0148a0001c0001t0006g0156a0001c0001t0006g0159others(21): Show | 24 | HG00544.hp2 HG00639.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1198-1872C>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168560 | ||||||
chr4:157168563
|
T | A | 1 | a0003c0009t0009g0107 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1198-1869T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168563 | ||||||
chr4:157168646
|
G | A | 10 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0007g0193others(7): Show | 10 | HG01192.hp1 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1198-1786G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157168646 | ||||||
chr4:157169181
|
G | A | 46 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0019others(43): Show | 48 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1198-1251G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169181 | ||||||
chr4:157169213
|
A | G | 2 | a0001c0001t0010g0256a0001c0001t0016g0176 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1198-1219A>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169213 | ||||||
chr4:157169714
|
A | C | 1 | a0005c0005t0006g0205 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1198-718A>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169714 | ||||||
chr4:157169729
|
G | T | 2 | a0001c0001t0005g0182a0001c0001t0014g0254 | 2 | HG01255.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1198-703G>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169729 | ||||||
chr4:157169834
|
G | A | 1 | a0001c0001t0002g0197 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1198-598G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169834 | ||||||
chr4:157169837
|
A | T | 81 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0019others(78): Show | 83 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.1198-595A>T | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169837 | ||||||
chr4:157169880
|
T | G | 10 | a0001c0001t0003g0026a0001c0001t0003g0074a0001c0001t0007g0193others(7): Show | 10 | HG01192.hp1 HG01981.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1198-552T>G | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169880 | ||||||
chr4:157169910
|
T | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0074 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1198-522T>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169910 | ||||||
chr4:157169941
|
G | C | 1 | a0001c0002t0006g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1198-491G>C | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169941 | ||||||
chr4:157169990
|
G | A | 1 | a0001c0003t0014g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1198-442G>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157169990 | ||||||
chr4:157170416
|
C | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0102 | 2 | NA19060.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1198-16C>A | GLRB | ENSG00000109738.11 | transcript | ENST00000264428.9 | protein_coding | 9/9 | chr4 | 157170416 |