geneid | 2800 |
---|---|
ensemblid | ENSG00000136935.14 |
hgncid | 4424 |
symbol | GOLGA1 |
name | golgin A1 |
refseq_nuc | NM_002077.4 |
refseq_prot | NP_002068.2 |
ensembl_nuc | ENST00000373555.9 |
ensembl_prot | ENSP00000362656.4 |
mane_status | MANE Select |
chr | chr9 |
start | 124878275 |
end | 124941083 |
strand | - |
ver | v1.2 |
region | chr9:124878275-124941083 |
region5000 | chr9:124873275-124946083 |
regionname0 | GOLGA1_chr9_124878275_124941083 |
regionname5000 | GOLGA1_chr9_124873275_124946083 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 767 | 183 | 41 | 44 | 69 | 10 | 19 | 52 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002 | 0/1 | 767 | 167 | 29 | 16 | 104 | 4 | 13 | 80 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0003 | 0/0 | 767 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0004 | 1/0 | 767 | 5 | 3 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0005 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0006 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0007 | 0/0 | 767 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0008 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0009 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0010 | 0/0 | 767 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0011 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0012 | 0/0 | 767 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2304 | 173 | 33 | 44 | 67 | 10 | 19 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0002 | 0/1 | 2304 | 103 | 18 | 14 | 60 | 4 | 6 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0003 | 0/0 | 2304 | 59 | 7 | 1 | 44 | 0 | 7 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0004 | 0/0 | 2304 | 11 | 9 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0005 | 0/0 | 2304 | 8 | 8 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0006 | 0/0 | 2304 | 5 | 4 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0007 | 1/0 | 2304 | 5 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0008 | 0/0 | 2304 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0009 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0010 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0011 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0012 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0013 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0014 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0015 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0016 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
c0017 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2574 | 153 | 19 | 15 | 101 | 4 | 13 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0002 | 0/0 | 2572 | 105 | 26 | 30 | 32 | 4 | 13 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0003 | 0/0 | 2574 | 52 | 12 | 9 | 19 | 6 | 6 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0004 | 0/0 | 2574 | 19 | 0 | 6 | 11 | 0 | 2 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0005 | 0/0 | 2574 | 8 | 8 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0006 | 0/0 | 2575 | 6 | 5 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0007 | 1/0 | 2574 | 5 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0008 | 0/0 | 2574 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0009 | 0/0 | 2575 | 4 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0010 | 0/0 | 2572 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0011 | 0/0 | 2574 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0012 | 0/0 | 2574 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0013 | 0/0 | 2574 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0014 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0015 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0016 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0017 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0018 | 0/0 | 2572 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0019 | 0/0 | 2572 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
t0020 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0011 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2304 | 173 | 33 | 44 | 67 | 10 | 19 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0005 | 0/0 | 2304 | 8 | 8 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0010 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0014 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0002 | 0/1 | 2304 | 103 | 18 | 14 | 60 | 4 | 6 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0003 | 0/0 | 2304 | 59 | 7 | 1 | 44 | 0 | 7 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0006 | 0/0 | 2304 | 5 | 4 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0003c0004 | 0/0 | 2304 | 11 | 9 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0004c0007 | 1/0 | 2304 | 5 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0005c0016 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0006c0013 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0007c0012 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0008c0011 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0009c0009 | 0/0 | 2304 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0010c0008 | 0/0 | 2304 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0011c0015 | 0/0 | 2304 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0012c0017 | 0/0 | 2304 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 4875 | 101 | 25 | 29 | 31 | 4 | 12 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0001t0003 | 0/0 | 4877 | 45 | 7 | 8 | 18 | 6 | 6 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0001t0004 | 0/0 | 4877 | 18 | 0 | 6 | 11 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0001t0008 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0001t0010 | 0/0 | 4875 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0001t0016 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0001t0017 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0001t0018 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0001t0019 | 0/0 | 4875 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0005t0005 | 0/0 | 4877 | 8 | 8 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0010t0002 | 0/0 | 4875 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0001c0014t0003 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0002t0001 | 0/1 | 4877 | 97 | 14 | 14 | 58 | 4 | 6 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0002t0008 | 0/0 | 4877 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0002t0011 | 0/0 | 4877 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0002t0020 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0003t0001 | 0/0 | 4877 | 55 | 4 | 1 | 43 | 0 | 7 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0003t0012 | 0/0 | 4877 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0003t0014 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0003t0015 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0002c0006t0003 | 0/0 | 4877 | 5 | 4 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0003c0004t0006 | 0/0 | 4878 | 6 | 5 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0003c0004t0009 | 0/0 | 4878 | 4 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0003c0004t0013 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0004c0007t0007 | 1/0 | 4877 | 5 | 3 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0005c0016t0001 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0006c0013t0002 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0007c0012t0002 | 0/0 | 4875 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0008c0011t0003 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0009c0009t0008 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0010c0008t0002 | 0/0 | 4875 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0011c0015t0013 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
a0012c0017t0004 | 0/0 | 4877 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | copy fasta | chr9 | 124873275 | 124946083 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0011 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0016g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0017g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0018g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0001t0019g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0005t0005g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0005t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0005t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0005t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0005t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0010t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0001c0014t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0008g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0011g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0011g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0002t0020g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0012g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0003t0015g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0006t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0006t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0006t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0006t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0002c0006t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0009g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0003c0004t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0004c0007t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0004c0007t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0004c0007t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0004c0007t0007g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0004c0007t0007g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0005c0016t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0006c0013t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0007c0012t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0008c0011t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0009c0009t0008g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0010c0008t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0011c0015t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
a0012c0017t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0090 | EUR | GBR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | GBR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0045 | EUR | GBR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0314 | EUR | GBR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0048 | EUR | FIN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | FIN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0201 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00438 | hp1 | a0002 | c0003 | t0001 | g0209 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00558 | hp1 | a0002 | c0003 | t0001 | g0194 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00597 | hp1 | a0002 | c0003 | t0001 | g0219 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00609 | hp1 | a0002 | c0003 | t0001 | g0196 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0216 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00639 | hp2 | a0003 | c0004 | t0009 | g0038 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0290 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0199 | EAS | CHS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01069 | hp2 | a0003 | c0004 | t0006 | g0062 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0313 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01074 | hp2 | a0010 | c0008 | t0002 | g0146 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0307 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01109 | hp1 | a0004 | c0007 | t0007 | g0054 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01167 | hp1 | a0002 | c0006 | t0003 | g0105 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01255 | hp1 | a0002 | c0003 | t0001 | g0200 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0242 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0262 | EUR | IBS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0287 | EUR | IBS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01884 | hp1 | a0003 | c0004 | t0009 | g0061 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01884 | hp2 | a0005 | c0016 | t0001 | g0110 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01981 | hp2 | a0001 | c0001 | t0019 | g0136 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0233 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02027 | hp1 | a0001 | c0001 | t0017 | g0240 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02027 | hp2 | a0002 | c0003 | t0001 | g0188 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02055 | hp2 | a0008 | c0011 | t0003 | g0078 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02071 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02071 | hp2 | a0001 | c0001 | t0018 | g0142 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02145 | hp1 | a0001 | c0005 | t0005 | g0332 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CDX | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | CDX | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02258 | hp1 | a0003 | c0004 | t0006 | g0065 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02258 | hp2 | a0002 | c0002 | t0011 | g0030 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02280 | hp1 | a0004 | c0007 | t0007 | g0053 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02451 | hp1 | a0001 | c0005 | t0005 | g0333 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02523 | hp1 | a0009 | c0009 | t0008 | g0036 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02523 | hp2 | a0002 | c0003 | t0001 | g0210 | EAS | KHV | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02572 | hp1 | a0004 | c0007 | t0007 | g0052 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0278 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02615 | hp2 | a0003 | c0004 | t0006 | g0064 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0317 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02630 | hp2 | a0001 | c0001 | t0016 | g0041 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02683 | hp1 | a0012 | c0017 | t0004 | g0055 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0203 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0285 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02717 | hp2 | a0001 | c0005 | t0005 | g0005 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02723 | hp1 | a0003 | c0004 | t0006 | g0059 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02723 | hp2 | a0002 | c0003 | t0001 | g0037 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0286 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02895 | hp1 | a0002 | c0006 | t0003 | g0106 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02897 | hp1 | a0002 | c0006 | t0003 | g0107 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02922 | hp1 | a0004 | c0007 | t0007 | g0051 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02965 | hp1 | a0002 | c0003 | t0014 | g0034 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02976 | hp2 | a0001 | c0005 | t0005 | g0005 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03130 | hp1 | a0001 | c0005 | t0005 | g0005 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03130 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03139 | hp1 | a0003 | c0004 | t0006 | g0248 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03139 | hp2 | a0001 | c0005 | t0005 | g0334 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03195 | hp1 | a0001 | c0005 | t0005 | g0033 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03195 | hp2 | a0002 | c0006 | t0003 | g0104 | AFR | ESN | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0326 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03225 | hp2 | a0003 | c0004 | t0009 | g0060 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0328 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03486 | hp1 | a0002 | c0002 | t0020 | g0331 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0318 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0277 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03540 | hp1 | a0002 | c0006 | t0003 | g0108 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03540 | hp2 | a0002 | c0002 | t0011 | g0030 | AFR | GWD | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03579 | hp1 | a0003 | c0004 | t0006 | g0063 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03710 | hp2 | a0002 | c0003 | t0001 | g0268 | SAS | PJL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03927 | hp1 | a0002 | c0003 | t0001 | g0191 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03927 | hp2 | a0002 | c0003 | t0001 | g0257 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0213 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG04115 | hp1 | a0007 | c0012 | t0002 | g0144 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG04115 | hp2 | a0002 | c0003 | t0001 | g0214 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0193 | SAS | BEB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | STU | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18522 | hp2 | a0001 | c0005 | t0005 | g0033 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | CHB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18612 | hp2 | a0002 | c0003 | t0001 | g0207 | EAS | CHB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18906 | hp1 | a0002 | c0003 | t0001 | g0019 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0208 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18952 | hp2 | a0002 | c0003 | t0001 | g0230 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0223 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18961 | hp2 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0215 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18977 | hp1 | a0002 | c0003 | t0001 | g0211 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18977 | hp2 | a0001 | c0001 | t0010 | g0245 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18980 | hp2 | a0001 | c0010 | t0002 | g0070 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18981 | hp1 | a0001 | c0001 | t0010 | g0244 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18982 | hp1 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18982 | hp2 | a0002 | c0002 | t0008 | g0254 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18983 | hp1 | a0002 | c0003 | t0001 | g0218 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0202 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18987 | hp1 | a0002 | c0003 | t0001 | g0217 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18987 | hp2 | a0002 | c0002 | t0008 | g0255 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18990 | hp2 | a0001 | c0001 | t0010 | g0246 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18991 | hp1 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0221 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19003 | hp2 | a0002 | c0003 | t0001 | g0206 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19005 | hp1 | a0002 | c0003 | t0001 | g0229 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19006 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19006 | hp2 | a0002 | c0003 | t0001 | g0231 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19012 | hp2 | a0002 | c0003 | t0001 | g0220 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19043 | hp1 | a0003 | c0004 | t0013 | g0040 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19054 | hp1 | a0002 | c0003 | t0001 | g0228 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19058 | hp1 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0212 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19065 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19067 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19076 | hp1 | a0002 | c0003 | t0001 | g0222 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19077 | hp2 | a0001 | c0014 | t0003 | g0102 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0224 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19083 | hp2 | a0001 | c0001 | t0010 | g0247 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19084 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19088 | hp1 | a0002 | c0003 | t0001 | g0225 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19091 | hp1 | a0002 | c0003 | t0001 | g0227 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | YRI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA20129 | hp1 | a0002 | c0002 | t0011 | g0315 | AFR | ASW | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | ASW | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0134 | EUR | TSI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0284 | EUR | TSI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | TSI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0042 | EUR | TSI | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | GIH | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0024 | SAS | GIH | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0241 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02486 | hp2 | a0003 | c0004 | t0009 | g0058 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG02559 | hp2 | a0002 | c0003 | t0012 | g0114 | AFR | ACB | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG03471 | hp2 | a0006 | c0013 | t0002 | g0164 | AFR | MSL | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG06807 | hp1 | a0011 | c0015 | t0013 | g0039 | AFR | USA | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
HG06807 | hp2 | a0002 | c0003 | t0001 | g0226 | AFR | USA | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA18955 | hp2 | a0002 | c0003 | t0015 | g0204 | EAS | JPT | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
NA21309 | hp2 | a0002 | c0003 | t0012 | g0113 | AFR | LWK | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0298 | REF | REF | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
homoSapiens_grch38 | hp1 | a0004 | c0007 | t0007 | g0281 | REF | REF | GOLGA1_chr9_124873275_124946083 | GOLGA1 | chr9 | 124873275 | 124946083 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:124881887
|
G | A | 1 | a0008 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.2033C>T | p.Ala678Val | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/23 | 2351/4877 | 2033/2304 | 678/767 | chr9 | 124881887 | ||
chr9:124882568
|
G | C | 1 | a0007 | 1 | HG04115.hp1 | missense_variant&splice_region_variant | MODERATE | c.1907C>G | p.Thr636Ser | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/23 | 2225/4877 | 1907/2304 | 636/767 | chr9 | 124882568 | ||
chr9:124889187
|
G | A | 1 | a0011 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1717C>T | p.Arg573Trp | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/23 | 2035/4877 | 1717/2304 | 573/767 | chr9 | 124889187 | ||
chr9:124889479
|
C | T | 1 | a0009 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1555G>A | p.Glu519Lys | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 17/23 | 1873/4877 | 1555/2304 | 519/767 | chr9 | 124889479 | ||
chr9:124899366
|
G | A | 1 | a0002 | 167 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(164): Show |
missense_variant | MODERATE | c.1274C>T | p.Thr425Met | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/23 | 1592/4877 | 1274/2304 | 425/767 | chr9 | 124899366 | ||
chr9:124899472
|
C | T | 1 | a0010 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1168G>A | p.Ala390Thr | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/23 | 1486/4877 | 1168/2304 | 390/767 | chr9 | 124899472 | ||
chr9:124908433
|
G | C | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1009C>G | p.Gln337Glu | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/23 | 1327/4877 | 1009/2304 | 337/767 | chr9 | 124908433 | ||
chr9:124911921
|
A | C | 11 | a0001a0002a0003others(8): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
missense_variant | MODERATE | c.949T>G | p.Leu317Val | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/23 | 1267/4877 | 949/2304 | 317/767 | chr9 | 124911921 | ||
chr9:124921795
|
T | C | 2 | a0003a0011 | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
missense_variant | MODERATE | c.659A>G | p.Asn220Ser | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/23 | 977/4877 | 659/2304 | 220/767 | chr9 | 124921795 | ||
chr9:124921796
|
T | G | 1 | a0005 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.658A>C | p.Asn220His | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/23 | 976/4877 | 658/2304 | 220/767 | chr9 | 124921796 | ||
chr9:124926719
|
T | C | 1 | a0012 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.422A>G | p.Gln141Arg | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/23 | 740/4877 | 422/2304 | 141/767 | chr9 | 124926719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:124881177
|
T | C | 2 | a0001c0010a0002c0002 | 104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
synonymous_variant | LOW | c.2217A>G | p.Glu739Glu | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/23 | 2535/4877 | 2217/2304 | 739/767 | chr9 | 124881177 | ||
chr9:124882525
|
A | T | 1 | a0002c0006 | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.1950T>A | p.Thr650Thr | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/23 | 2268/4877 | 1950/2304 | 650/767 | chr9 | 124882525 | ||
chr9:124888352
|
A | C | 1 | a0001c0005 | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.1806T>G | p.Thr602Thr | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/23 | 2124/4877 | 1806/2304 | 602/767 | chr9 | 124888352 | ||
chr9:124889170
|
G | A | 2 | a0003c0004a0011c0015 | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
synonymous_variant | LOW | c.1734C>T | p.Ala578Ala | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/23 | 2052/4877 | 1734/2304 | 578/767 | chr9 | 124889170 | ||
chr9:124921240
|
T | C | 1 | a0001c0014 | 1 | NA19077.hp2 | splice_region_variant&synonymous_variant | LOW | c.732A>G | p.Arg244Arg | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/23 | 1050/4877 | 732/2304 | 244/767 | chr9 | 124921240 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:124878475
|
T | G | 1 | a0003c0004t0006 | 6 | HG01069.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2055A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 2055 | chr9 | 124878475 | |||||
chr9:124878487
|
G | A | 3 | a0001c0005t0005a0003c0004t0013a0011c0015t0013 | 10 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2043C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 2043 | chr9 | 124878487 | |||||
chr9:124878491
|
G | A | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2039C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 2039 | chr9 | 124878491 | |||||
chr9:124878503
|
A | G | 1 | a0002c0003t0012 | 2 | HG02559.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2027T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 2027 | chr9 | 124878503 | |||||
chr9:124878699
|
T | TG | 2 | a0003c0004t0006a0003c0004t0009 | 10 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1830dupC | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1830 | chr9 | 124878699 | |||||
chr9:124878713
|
C | T | 1 | a0002c0003t0012 | 2 | HG02559.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1817G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1817 | chr9 | 124878713 | |||||
chr9:124878759
|
T | C | 32 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(29): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
3_prime_UTR_variant | MODIFIER | c.*1771A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1771 | chr9 | 124878759 | |||||
chr9:124879319
|
T | A | 1 | a0001c0001t0017 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1211A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1211 | chr9 | 124879319 | |||||
chr9:124879356
|
C | T | 1 | a0002c0003t0015 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1174G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1174 | chr9 | 124879356 | |||||
chr9:124879386
|
T | C | 3 | a0001c0001t0008a0002c0002t0008a0009c0009t0008 | 4 | HG02523.hp1 NA18982.hp2 NA18987.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1144A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1144 | chr9 | 124879386 | |||||
chr9:124879446
|
G | A | 1 | a0001c0001t0018 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1084C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1084 | chr9 | 124879446 | |||||
chr9:124879448
|
A | G | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1082T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1082 | chr9 | 124879448 | |||||
chr9:124879485
|
G | A | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1045C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 1045 | chr9 | 124879485 | |||||
chr9:124879753
|
CAT | C | 8 | a0001c0001t0002a0001c0001t0010a0001c0001t0018others(5): Show | 111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*775_*776delAT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 775 | chr9 | 124879753 | |||||
chr9:124879857
|
A | T | 4 | a0001c0001t0003a0001c0014t0003a0002c0006t0003others(1): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*673T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 673 | chr9 | 124879857 | |||||
chr9:124879952
|
A | G | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
3_prime_UTR_variant | MODIFIER | c.*578T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 578 | chr9 | 124879952 | |||||
chr9:124880073
|
T | C | 1 | a0001c0001t0019 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 23/23 | 457 | chr9 | 124880073 | |||||
chr9:124938807
|
C | T | 1 | a0002c0002t0011 | 3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-96G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/23 | 96 | chr9 | 124938807 | |||||
chr9:124940134
|
T | C | 1 | a0001c0001t0010 | 4 | NA18977.hp2 NA18981.hp1 NA18990.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-184A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/23 | 1423 | chr9 | 124940134 | |||||
chr9:124941034
|
G | T | 1 | a0002c0003t0014 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-269C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/23 | 2323 | chr9 | 124941034 | |||||
chr9:124941050
|
G | A | 1 | a0002c0002t0020 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-285C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/23 | 2339 | chr9 | 124941050 | |||||
chr9:124941072
|
C | A | 1 | a0001c0005t0005 | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-307G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/23 | 2361 | chr9 | 124941072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:124880643
|
C | G | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2224-33G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880643 | ||||||
chr9:124880649
|
A | G | 3 | a0001c0001t0002g0112a0001c0001t0002g0118a0001c0001t0002g0249 | 3 | HG01109.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2224-39T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880649 | ||||||
chr9:124880802
|
G | C | 121 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(118): Show | 133 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.2224-192C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880802 | ||||||
chr9:124880889
|
T | C | 200 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(197): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.2224-279A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880889 | ||||||
chr9:124880897
|
C | T | 328 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(325): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.2223+274G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124880897 | ||||||
chr9:124881132
|
G | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2223+39C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 22/22 | chr9 | 124881132 | ||||||
chr9:124881306
|
G | A | 1 | a0003c0004t0013g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2137-49C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881306 | ||||||
chr9:124881327
|
C | T | 2 | a0002c0002t0001g0310a0002c0002t0001g0311 | 2 | NA18945.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2137-70G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881327 | ||||||
chr9:124881438
|
C | G | 1 | a0002c0003t0014g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2137-181G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881438 | ||||||
chr9:124881440
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2137-183A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881440 | ||||||
chr9:124881481
|
T | A | 107 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(104): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.2137-224A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881481 | ||||||
chr9:124881526
|
G | A | 1 | a0002c0003t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2136+258C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881526 | ||||||
chr9:124881667
|
A | G | 48 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(45): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.2136+117T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881667 | ||||||
chr9:124881672
|
G | A | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2136+112C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881672 | ||||||
chr9:124881710
|
T | TG | 26 | a0002c0002t0001g0024a0002c0002t0001g0026a0002c0002t0001g0027others(23): Show | 31 | HG00140.hp2 HG00673.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2136+73dupC | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 21/22 | chr9 | 124881710 | ||||||
chr9:124882017
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1966-63C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882017 | ||||||
chr9:124882031
|
G | A | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1966-77C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882031 | ||||||
chr9:124882095
|
T | G | 7 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(4): Show | 10 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1966-141A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882095 | ||||||
chr9:124882098
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1966-144C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882098 | ||||||
chr9:124882123
|
G | C | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1966-169C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882123 | ||||||
chr9:124882163
|
T | C | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1966-209A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882163 | ||||||
chr9:124882214
|
C | CCA | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1966-262_1966-261d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882214 | ||||||
chr9:124882318
|
C | T | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0290 | 3 | HG00642.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1965+192G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882318 | ||||||
chr9:124882319
|
G | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1965+191C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882319 | ||||||
chr9:124882334
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1965+176C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882334 | ||||||
chr9:124882336
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1965+174C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882336 | ||||||
chr9:124882405
|
G | T | 7 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(4): Show | 10 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1965+105C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882405 | ||||||
chr9:124882428
|
C | T | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1965+82G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 20/22 | chr9 | 124882428 | ||||||
chr9:124882603
|
G | A | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1906-34C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882603 | ||||||
chr9:124882858
|
G | A | 1 | a0002c0003t0001g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1906-289C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882858 | ||||||
chr9:124882863
|
G | A | 15 | a0002c0003t0001g0001a0002c0003t0001g0190a0002c0003t0001g0196others(12): Show | 18 | HG00609.hp1 HG00673.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.1906-294C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882863 | ||||||
chr9:124882925
|
A | G | 321 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(318): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1906-356T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882925 | ||||||
chr9:124882962
|
C | T | 14 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0020others(11): Show | 17 | HG00733.hp2 HG00741.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1906-393G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882962 | ||||||
chr9:124882963
|
G | A | 1 | a0001c0001t0004g0021 | 2 | HG00621.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1906-394C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124882963 | ||||||
chr9:124883006
|
G | T | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1906-437C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883006 | ||||||
chr9:124883104
|
AT | A | 93 | a0001c0001t0002g0014a0001c0001t0002g0119a0001c0001t0002g0162others(90): Show | 109 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1906-536delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883104 | ||||||
chr9:124883185
|
C | T | 4 | a0002c0002t0001g0288a0002c0002t0001g0295a0002c0002t0001g0296others(1): Show | 4 | NA18964.hp2 NA18995.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906-616G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883185 | ||||||
chr9:124883258
|
G | C | 110 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(107): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1906-689C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883258 | ||||||
chr9:124883292
|
CT | C | 17 | a0001c0001t0002g0129a0001c0001t0004g0003a0001c0001t0004g0021others(14): Show | 21 | HG00621.hp1 HG01123.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1906-724delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883292 | ||||||
chr9:124883609
|
G | A | 2 | a0002c0002t0011g0030a0002c0002t0011g0315 | 3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1906-1040C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883609 | ||||||
chr9:124883848
|
G | A | 2 | a0002c0002t0001g0321a0002c0002t0001g0325 | 2 | HG02080.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1906-1279C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883848 | ||||||
chr9:124883871
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1906-1302G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883871 | ||||||
chr9:124883901
|
GTTT | G | 3 | a0002c0002t0001g0002a0002c0002t0001g0253a0002c0002t0001g0273 | 6 | NA18989.hp1 NA18998.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1906-1335_1906-133 others(7): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883901 | ||||||
chr9:124883937
|
A | G | 48 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(45): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1906-1368T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883937 | ||||||
chr9:124883979
|
T | G | 1 | a0002c0002t0001g0262 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1906-1410A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124883979 | ||||||
chr9:124884016
|
A | T | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0056others(3): Show | 8 | NA18955.hp1 NA18960.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.1906-1447T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884016 | ||||||
chr9:124884016
|
AT | A | 6 | a0001c0001t0003g0089a0001c0001t0004g0237a0002c0002t0001g0274others(3): Show | 6 | HG00558.hp1 HG02486.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906-1448delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884016 | ||||||
chr9:124884018
|
T | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1906-1449A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884018 | ||||||
chr9:124884034
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1906-1465G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884034 | ||||||
chr9:124884074
|
C | T | 60 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(57): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1906-1505G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884074 | ||||||
chr9:124884246
|
A | AGGTGAT | 48 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(45): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1906-1683_1906-167 others(10): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884246 | ||||||
chr9:124884400
|
A | C | 2 | a0002c0002t0001g0310a0002c0002t0001g0311 | 2 | NA18945.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1906-1831T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884400 | ||||||
chr9:124884405
|
G | A | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1906-1836C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884405 | ||||||
chr9:124884499
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1906-1930G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884499 | ||||||
chr9:124884500
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1906-1931C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884500 | ||||||
chr9:124884764
|
C | G | 1 | a0001c0001t0003g0092 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1906-2195G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884764 | ||||||
chr9:124884777
|
C | T | 2 | a0002c0003t0012g0113a0002c0003t0012g0114 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1906-2208G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884777 | ||||||
chr9:124884883
|
G | C | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0290 | 3 | HG00642.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1906-2314C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124884883 | ||||||
chr9:124885121
|
G | A | 2 | a0003c0004t0013g0040a0011c0015t0013g0039 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1906-2552C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885121 | ||||||
chr9:124885133
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1906-2564G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885133 | ||||||
chr9:124885188
|
G | A | 1 | a0001c0001t0004g0232 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1906-2619C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885188 | ||||||
chr9:124885306
|
G | A | 12 | a0002c0003t0012g0113a0002c0003t0012g0114a0003c0004t0006g0059others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1906-2737C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885306 | ||||||
chr9:124885322
|
C | CA | 9 | a0001c0001t0002g0187a0001c0001t0016g0041a0001c0005t0005g0005others(6): Show | 12 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1906-2754dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885322 | ||||||
chr9:124885322
|
C | CAA | 139 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(136): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1906-2755_1906-275 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885322 | ||||||
chr9:124885322
|
C | CAAA | 6 | a0001c0001t0002g0116a0001c0001t0002g0159a0001c0001t0002g0166others(3): Show | 6 | HG02622.hp2 NA18906.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1906-2756_1906-275 others(7): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885322 | ||||||
chr9:124885440
|
A | G | 8 | a0001c0001t0016g0041a0001c0005t0005g0005a0001c0005t0005g0033others(5): Show | 11 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1905+2813T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885440 | ||||||
chr9:124885442
|
G | A | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1905+2811C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885442 | ||||||
chr9:124885484
|
CA | C | 180 | a0001c0001t0002g0140a0001c0001t0003g0080a0001c0001t0004g0003others(177): Show | 208 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.1905+2768delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885484 | ||||||
chr9:124885521
|
G | A | 92 | a0001c0001t0008g0035a0002c0002t0001g0002a0002c0002t0001g0004others(89): Show | 107 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1905+2732C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885521 | ||||||
chr9:124885571
|
GGGA | G | 180 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(177): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1905+2679_1905+268 others(7): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885571 | ||||||
chr9:124885903
|
C | T | 57 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0020others(54): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1905+2350G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885903 | ||||||
chr9:124885977
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1905+2276C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885977 | ||||||
chr9:124885980
|
G | A | 3 | a0003c0004t0009g0058a0003c0004t0009g0060a0003c0004t0009g0061 | 3 | HG01884.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1905+2273C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124885980 | ||||||
chr9:124886075
|
A | G | 14 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0120others(11): Show | 16 | HG00280.hp2 HG01074.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1905+2178T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886075 | ||||||
chr9:124886411
|
G | GC | 48 | a0002c0003t0001g0001a0002c0003t0001g0017a0002c0003t0001g0018others(45): Show | 54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1905+1841_1905+184 others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886411 | ||||||
chr9:124886412
|
G | A | 48 | a0002c0003t0001g0001a0002c0003t0001g0017a0002c0003t0001g0018others(45): Show | 54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1905+1841C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886412 | ||||||
chr9:124886413
|
C | G | 48 | a0002c0003t0001g0001a0002c0003t0001g0017a0002c0003t0001g0018others(45): Show | 54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1905+1840G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886413 | ||||||
chr9:124886568
|
T | C | 1 | a0002c0003t0001g0219 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1905+1685A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886568 | ||||||
chr9:124886634
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1905+1619T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886634 | ||||||
chr9:124886649
|
C | T | 41 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0115others(38): Show | 43 | HG00280.hp2 HG00423.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1905+1604G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886649 | ||||||
chr9:124886655
|
A | G | 1 | a0002c0002t0001g0025 | 2 | HG01099.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1905+1598T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886655 | ||||||
chr9:124886713
|
G | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1905+1540C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886713 | ||||||
chr9:124886927
|
G | A | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1905+1326C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124886927 | ||||||
chr9:124887087
|
A | T | 1 | a0002c0002t0001g0312 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1905+1166T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887087 | ||||||
chr9:124887142
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1905+1111G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887142 | ||||||
chr9:124887266
|
T | C | 2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1905+987A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887266 | ||||||
chr9:124887298
|
A | T | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1905+955T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887298 | ||||||
chr9:124887327
|
G | A | 2 | a0001c0001t0002g0112a0001c0001t0002g0118 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1905+926C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887327 | ||||||
chr9:124887339
|
A | AGGGCTGG others(12): Show |
1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1905+895_1905+913d others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887339 | ||||||
chr9:124887350
|
G | A | 10 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(7): Show | 10 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1905+903C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887350 | ||||||
chr9:124887401
|
G | A | 1 | a0002c0002t0001g0271 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1905+852C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887401 | ||||||
chr9:124887428
|
T | A | 8 | a0002c0003t0001g0018a0002c0003t0001g0191a0002c0003t0001g0194others(5): Show | 9 | HG00558.hp1 HG00597.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.1905+825A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887428 | ||||||
chr9:124887519
|
T | C | 1 | a0001c0001t0003g0086 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1905+734A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887519 | ||||||
chr9:124887553
|
G | A | 1 | a0002c0003t0014g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1905+700C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887553 | ||||||
chr9:124887751
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1905+502C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887751 | ||||||
chr9:124887868
|
C | T | 1 | a0001c0001t0003g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1905+385G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124887868 | ||||||
chr9:124888042
|
G | C | 149 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(146): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1905+211C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124888042 | ||||||
chr9:124888048
|
G | A | 6 | a0001c0001t0002g0168a0001c0001t0002g0170a0001c0001t0002g0183others(3): Show | 6 | HG00408.hp1 HG02040.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1905+205C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124888048 | ||||||
chr9:124888072
|
TGGA | T | 4 | a0001c0001t0003g0008a0001c0001t0003g0056a0001c0001t0003g0087others(1): Show | 5 | NA18960.hp1 NA18961.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1905+178_1905+180d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 19/22 | chr9 | 124888072 | ||||||
chr9:124888545
|
A | G | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1762-149T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888545 | ||||||
chr9:124888576
|
C | T | 1 | a0002c0003t0001g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1762-180G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888576 | ||||||
chr9:124888630
|
G | C | 170 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(167): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1762-234C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888630 | ||||||
chr9:124888650
|
T | C | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1762-254A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888650 | ||||||
chr9:124888688
|
CTTTA | C | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1762-296_1762-293d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888688 | ||||||
chr9:124888706
|
T | C | 170 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(167): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1762-310A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888706 | ||||||
chr9:124888781
|
G | T | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1761+362C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888781 | ||||||
chr9:124888835
|
G | A | 1 | a0002c0003t0001g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1761+308C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888835 | ||||||
chr9:124888971
|
T | A | 86 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0023others(83): Show | 101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1761+172A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124888971 | ||||||
chr9:124889059
|
C | A | 1 | a0002c0002t0020g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1761+84G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124889059 | ||||||
chr9:124889062
|
C | T | 107 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(104): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1761+81G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124889062 | ||||||
chr9:124889105
|
C | T | 3 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0019g0136 | 3 | HG01952.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1761+38G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 18/22 | chr9 | 124889105 | ||||||
chr9:124889800
|
C | G | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1498-264G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124889800 | ||||||
chr9:124890000
|
G | C | 22 | a0001c0001t0002g0015a0001c0001t0002g0161a0001c0001t0002g0168others(19): Show | 23 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1497+389C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890000 | ||||||
chr9:124890018
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1497+371T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890018 | ||||||
chr9:124890092
|
T | C | 1 | a0002c0002t0001g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1497+297A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890092 | ||||||
chr9:124890181
|
C | A | 47 | a0002c0003t0001g0001a0002c0003t0001g0017a0002c0003t0001g0018others(44): Show | 53 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1497+208G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890181 | ||||||
chr9:124890342
|
G | A | 90 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0023others(87): Show | 105 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1497+47C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890342 | ||||||
chr9:124890381
|
G | C | 2 | a0002c0003t0012g0113a0002c0003t0012g0114 | 2 | HG02559.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.1497+8C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 16/22 | chr9 | 124890381 | ||||||
chr9:124890532
|
G | A | 11 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(8): Show | 11 | HG01069.hp2 HG01884.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408-54C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890532 | ||||||
chr9:124890562
|
G | A | 1 | a0002c0002t0001g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1408-84C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890562 | ||||||
chr9:124890720
|
C | T | 3 | a0002c0003t0001g0229a0002c0003t0001g0230a0002c0003t0001g0231 | 3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1408-242G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890720 | ||||||
chr9:124890726
|
C | T | 103 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1408-248G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890726 | ||||||
chr9:124890788
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1408-310C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890788 | ||||||
chr9:124890820
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-342C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890820 | ||||||
chr9:124890856
|
AAAG | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408-381_1408-379d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890856 | ||||||
chr9:124890964
|
G | C | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1408-486C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124890964 | ||||||
chr9:124891200
|
C | G | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1408-722G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891200 | ||||||
chr9:124891207
|
C | A | 1 | a0001c0001t0002g0139 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1408-729G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891207 | ||||||
chr9:124891222
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-744C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891222 | ||||||
chr9:124891222
|
G | C | 143 | a0001c0001t0008g0035a0002c0002t0001g0002a0002c0002t0001g0004others(140): Show | 164 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1408-744C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891222 | ||||||
chr9:124891306
|
G | A | 2 | a0002c0003t0001g0192a0002c0003t0001g0206 | 2 | NA19000.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1408-828C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891306 | ||||||
chr9:124891378
|
C | A | 1 | a0002c0002t0001g0317 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1408-900G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891378 | ||||||
chr9:124891551
|
T | A | 1 | a0002c0002t0001g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1408-1073A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891551 | ||||||
chr9:124891678
|
CTT | C | 6 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(3): Show | 6 | HG01069.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-1202_1408-120 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891678 | ||||||
chr9:124891681
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-1203C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891681 | ||||||
chr9:124891764
|
C | G | 4 | a0002c0002t0001g0025a0002c0002t0001g0032a0002c0002t0001g0271others(1): Show | 6 | HG01099.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-1286G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891764 | ||||||
chr9:124891770
|
G | A | 1 | a0002c0002t0001g0294 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1408-1292C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891770 | ||||||
chr9:124891774
|
A | G | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408-1296T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891774 | ||||||
chr9:124891978
|
C | CAG | 323 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(320): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1408-1502_1408-150 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124891978 | ||||||
chr9:124892081
|
G | T | 1 | a0002c0003t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1408-1603C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892081 | ||||||
chr9:124892249
|
C | T | 1 | a0002c0003t0001g0225 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1408-1771G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892249 | ||||||
chr9:124892250
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1408-1772C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892250 | ||||||
chr9:124892252
|
G | C | 1 | a0002c0003t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1408-1774C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892252 | ||||||
chr9:124892253
|
C | G | 1 | a0002c0003t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1408-1775G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892253 | ||||||
chr9:124892315
|
G | A | 1 | a0002c0003t0001g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1408-1837C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892315 | ||||||
chr9:124892338
|
T | C | 152 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(149): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1408-1860A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892338 | ||||||
chr9:124892707
|
C | T | 1 | a0002c0002t0001g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1408-2229G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892707 | ||||||
chr9:124892793
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-2315C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892793 | ||||||
chr9:124892888
|
C | T | 1 | a0002c0002t0001g0263 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1408-2410G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892888 | ||||||
chr9:124892893
|
T | C | 1 | a0002c0002t0001g0263 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1408-2415A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892893 | ||||||
chr9:124892932
|
C | CA | 140 | a0001c0001t0008g0035a0001c0001t0010g0244a0002c0002t0001g0002others(137): Show | 161 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1408-2455dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892932 | ||||||
chr9:124892954
|
G | T | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0128others(6): Show | 11 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1408-2476C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892954 | ||||||
chr9:124892977
|
A | T | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-2499T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892977 | ||||||
chr9:124892999
|
T | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-2521A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124892999 | ||||||
chr9:124893106
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1408-2628G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893106 | ||||||
chr9:124893226
|
T | A | 1 | a0011c0015t0013g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1408-2748A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893226 | ||||||
chr9:124893311
|
C | G | 3 | a0001c0001t0002g0112a0001c0001t0002g0118a0001c0001t0002g0249 | 3 | HG01109.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1408-2833G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893311 | ||||||
chr9:124893486
|
C | T | 2 | a0002c0002t0001g0294a0002c0002t0001g0298 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1408-3008G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893486 | ||||||
chr9:124893546
|
G | A | 1 | a0002c0003t0001g0198 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1408-3068C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893546 | ||||||
chr9:124893554
|
C | T | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1408-3076G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893554 | ||||||
chr9:124893677
|
C | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408-3199G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893677 | ||||||
chr9:124893817
|
T | C | 11 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0120others(8): Show | 13 | HG01081.hp2 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1408-3339A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893817 | ||||||
chr9:124893888
|
T | G | 1 | a0001c0001t0002g0299 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1408-3410A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893888 | ||||||
chr9:124893924
|
G | A | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1408-3446C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893924 | ||||||
chr9:124893947
|
C | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1408-3469G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124893947 | ||||||
chr9:124894276
|
C | G | 2 | a0002c0003t0001g0257a0002c0003t0001g0268 | 2 | HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1408-3798G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894276 | ||||||
chr9:124894380
|
T | TTG | 11 | a0001c0001t0003g0048a0001c0001t0004g0233a0001c0005t0005g0005others(8): Show | 14 | HG00280.hp1 HG00738.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1408-3904_1408-390 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894380 | ||||||
chr9:124894380
|
TTG | T | 189 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(186): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1408-3904_1408-390 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894380 | ||||||
chr9:124894380
|
TTGTG | T | 10 | a0001c0001t0002g0015a0001c0001t0002g0171a0001c0001t0002g0173others(7): Show | 11 | HG01167.hp1 HG01884.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408-3906_1408-390 others(8): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894380 | ||||||
chr9:124894482
|
C | T | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1408-4004G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894482 | ||||||
chr9:124894536
|
A | G | 4 | a0002c0002t0001g0025a0002c0002t0001g0032a0002c0002t0001g0271others(1): Show | 6 | HG01099.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+4013T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894536 | ||||||
chr9:124894585
|
G | C | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1407+3964C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894585 | ||||||
chr9:124894650
|
T | G | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1407+3899A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894650 | ||||||
chr9:124894747
|
A | G | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1407+3802T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894747 | ||||||
chr9:124894900
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0118 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1407+3649G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894900 | ||||||
chr9:124894949
|
C | CACATCCA others(27): Show |
1 | a0002c0002t0020g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1407+3599_1407+360 others(38): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894949 | ||||||
chr9:124894949
|
C | CCCATCCA others(27): Show |
91 | a0001c0001t0008g0035a0002c0002t0001g0002a0002c0002t0001g0004others(88): Show | 106 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1407+3566_1407+359 others(38): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894949 | ||||||
chr9:124894961
|
A | G | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1407+3588T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894961 | ||||||
chr9:124894965
|
A | T | 5 | a0001c0001t0002g0016a0001c0001t0002g0120a0001c0001t0002g0137others(2): Show | 6 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+3584T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894965 | ||||||
chr9:124894969
|
ATCCACAA others(10): Show |
A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1407+3563_1407+357 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894969 | ||||||
chr9:124894970
|
T | A | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1407+3579A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124894970 | ||||||
chr9:124895115
|
A | T | 8 | a0002c0003t0001g0017a0002c0003t0001g0192a0002c0003t0001g0193others(5): Show | 9 | HG00438.hp1 HG00621.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+3434T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895115 | ||||||
chr9:124895150
|
TCTCCACA others(9): Show |
T | 1 | a0002c0002t0001g0276 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1407+3383_1407+339 others(20): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895150 | ||||||
chr9:124895268
|
ATCCACAA others(140): Show |
A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+3134_1407+328 others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895268 | ||||||
chr9:124895302
|
CTCCACAA others(10): Show |
C | 1 | a0002c0002t0001g0285 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1407+3230_1407+324 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895302 | ||||||
chr9:124895348
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1407+3201T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895348 | ||||||
chr9:124895365
|
TCTCCACA others(42): Show |
T | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1407+3135_1407+318 others(53): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895365 | ||||||
chr9:124895445
|
A | AACCCTCC others(26): Show |
1 | a0002c0002t0001g0317 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1407+3071_1407+310 others(37): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895445 | ||||||
chr9:124895567
|
C | T | 1 | a0002c0003t0001g0220 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1407+2982G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895567 | ||||||
chr9:124895624
|
G | GGAGCCTC others(9): Show |
1 | a0001c0001t0002g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1407+2909_1407+292 others(20): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895624 | ||||||
chr9:124895795
|
T | A | 1 | a0002c0003t0014g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1407+2754A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895795 | ||||||
chr9:124895806
|
GACCCTCC others(10): Show |
G | 7 | a0001c0001t0002g0160a0001c0001t0003g0048a0001c0001t0003g0089others(4): Show | 7 | HG00280.hp1 HG01081.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1407+2726_1407+274 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895806 | ||||||
chr9:124895859
|
C | T | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1407+2690G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895859 | ||||||
chr9:124895862
|
TCCACAAC others(10): Show |
T | 6 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(3): Show | 6 | HG01069.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1407+2670_1407+268 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895862 | ||||||
chr9:124895896
|
CCCACAAC others(10): Show |
C | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1407+2636_1407+265 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895896 | ||||||
chr9:124895900
|
CAACAGAG others(42): Show |
C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+2600_1407+264 others(53): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895900 | ||||||
chr9:124895939
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1407+2610T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895939 | ||||||
chr9:124895947
|
T | C | 1 | a0002c0002t0001g0329 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1407+2602A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895947 | ||||||
chr9:124895948
|
A | G | 92 | a0001c0001t0008g0035a0002c0002t0001g0002a0002c0002t0001g0004others(89): Show | 107 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1407+2601T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895948 | ||||||
chr9:124895949
|
T | TAACAGAG others(10): Show |
1 | a0002c0002t0001g0329 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1407+2583_1407+259 others(21): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895949 | ||||||
chr9:124895968
|
A | G | 1 | a0001c0001t0003g0042 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1407+2581T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124895968 | ||||||
chr9:124896014
|
C | T | 2 | a0001c0001t0003g0050a0001c0001t0003g0085 | 2 | HG02135.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1407+2535G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896014 | ||||||
chr9:124896191
|
A | G | 92 | a0001c0001t0008g0035a0002c0002t0001g0002a0002c0002t0001g0004others(89): Show | 107 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1407+2358T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896191 | ||||||
chr9:124896284
|
C | T | 86 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0023others(83): Show | 101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1407+2265G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896284 | ||||||
chr9:124896319
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1407+2230T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896319 | ||||||
chr9:124896606
|
C | A | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1407+1943G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896606 | ||||||
chr9:124896756
|
A | G | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1407+1793T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896756 | ||||||
chr9:124896890
|
C | T | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1407+1659G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896890 | ||||||
chr9:124896931
|
CA | C | 6 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(3): Show | 9 | HG00558.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+1617delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896931 | ||||||
chr9:124896997
|
C | T | 1 | a0002c0003t0001g0201 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1407+1552G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124896997 | ||||||
chr9:124897067
|
T | C | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1407+1482A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897067 | ||||||
chr9:124897120
|
T | C | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1407+1429A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897120 | ||||||
chr9:124897132
|
T | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+1417A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897132 | ||||||
chr9:124897513
|
G | T | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1407+1036C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897513 | ||||||
chr9:124897623
|
G | T | 7 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0056others(4): Show | 9 | NA18955.hp1 NA18960.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+926C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897623 | ||||||
chr9:124897703
|
T | C | 1 | a0002c0002t0001g0251 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1407+846A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897703 | ||||||
chr9:124897796
|
A | C | 1 | a0001c0001t0017g0240 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1407+753T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897796 | ||||||
chr9:124897808
|
G | T | 1 | a0002c0003t0001g0217 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1407+741C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897808 | ||||||
chr9:124897931
|
G | T | 164 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(161): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1407+618C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897931 | ||||||
chr9:124897985
|
T | G | 32 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0115others(29): Show | 34 | HG00280.hp2 HG00423.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1407+564A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124897985 | ||||||
chr9:124898068
|
T | C | 10 | a0002c0002t0001g0004a0002c0002t0001g0308a0002c0002t0001g0309others(7): Show | 12 | HG00438.hp2 HG02080.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1407+481A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898068 | ||||||
chr9:124898129
|
C | G | 72 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(69): Show | 76 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1407+420G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898129 | ||||||
chr9:124898233
|
C | T | 2 | a0002c0002t0001g0261a0002c0002t0001g0305 | 2 | NA18965.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1407+316G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898233 | ||||||
chr9:124898354
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+195C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898354 | ||||||
chr9:124898414
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1407+135C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898414 | ||||||
chr9:124898424
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1407+125T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 15/22 | chr9 | 124898424 | ||||||
chr9:124898792
|
G | T | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-148C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898792 | ||||||
chr9:124898914
|
G | A | 1 | a0002c0002t0001g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1312-270C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898914 | ||||||
chr9:124898929
|
C | G | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1312-285G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898929 | ||||||
chr9:124898952
|
T | G | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-308A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898952 | ||||||
chr9:124898990
|
G | A | 1 | a0006c0013t0002g0164 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1311+339C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124898990 | ||||||
chr9:124899021
|
C | T | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+308G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899021 | ||||||
chr9:124899128
|
C | T | 3 | a0003c0004t0006g0059a0003c0004t0006g0064a0003c0004t0006g0065 | 3 | HG02258.hp1 HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1311+201G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899128 | ||||||
chr9:124899242
|
T | C | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1311+87A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899242 | ||||||
chr9:124899247
|
A | C | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1311+82T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899247 | ||||||
chr9:124899262
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1311+67G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899262 | ||||||
chr9:124899294
|
C | T | 1 | a0002c0002t0020g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1311+35G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 14/22 | chr9 | 124899294 | ||||||
chr9:124899483
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG00597.hp2 | splice_region_variant&intron_variant | LOW | c.1162-5C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899483 | ||||||
chr9:124899618
|
C | A | 1 | a0002c0003t0001g0207 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1162-140G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899618 | ||||||
chr9:124899850
|
C | G | 166 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1162-372G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899850 | ||||||
chr9:124899874
|
A | G | 3 | a0003c0004t0006g0059a0003c0004t0006g0064a0003c0004t0006g0065 | 3 | HG02258.hp1 HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1162-396T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899874 | ||||||
chr9:124899881
|
G | A | 1 | a0002c0002t0001g0279 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-403C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899881 | ||||||
chr9:124899882
|
G | C | 1 | a0002c0002t0001g0279 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-404C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899882 | ||||||
chr9:124899883
|
C | A | 1 | a0002c0002t0001g0279 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-405G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899883 | ||||||
chr9:124899886
|
C | T | 1 | a0002c0002t0001g0279 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-408G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899886 | ||||||
chr9:124899896
|
G | T | 1 | a0002c0002t0001g0279 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1162-418C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899896 | ||||||
chr9:124899950
|
T | A | 1 | a0002c0002t0001g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1162-472A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124899950 | ||||||
chr9:124900027
|
G | A | 1 | a0002c0002t0001g0274 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1161+425C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900027 | ||||||
chr9:124900057
|
T | C | 48 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(45): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1161+395A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900057 | ||||||
chr9:124900146
|
G | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(107): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1161+306C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900146 | ||||||
chr9:124900217
|
G | T | 1 | a0001c0001t0003g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1161+235C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900217 | ||||||
chr9:124900269
|
C | G | 137 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0023others(134): Show | 158 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1161+183G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900269 | ||||||
chr9:124900305
|
T | C | 51 | a0002c0003t0001g0001a0002c0003t0001g0017a0002c0003t0001g0018others(48): Show | 57 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1161+147A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900305 | ||||||
chr9:124900370
|
C | T | 1 | a0002c0002t0001g0307 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1161+82G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900370 | ||||||
chr9:124900377
|
A | G | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1161+75T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 13/22 | chr9 | 124900377 | ||||||
chr9:124900556
|
G | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1066-9C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124900556 | ||||||
chr9:124900970
|
A | AT | 20 | a0001c0001t0002g0130a0001c0001t0002g0132a0001c0001t0002g0155others(17): Show | 22 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1066-424dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124900970 | ||||||
chr9:124900970
|
AT | A | 52 | a0001c0001t0003g0056a0001c0001t0003g0086a0001c0001t0003g0087others(49): Show | 59 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1066-424delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124900970 | ||||||
chr9:124900994
|
T | C | 328 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(325): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1066-447A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124900994 | ||||||
chr9:124901037
|
T | C | 122 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(119): Show | 130 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1066-490A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901037 | ||||||
chr9:124901072
|
C | T | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1066-525G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901072 | ||||||
chr9:124901246
|
C | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1066-699G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901246 | ||||||
chr9:124901272
|
A | AT | 10 | a0001c0001t0002g0112a0001c0001t0002g0118a0001c0001t0010g0245others(7): Show | 10 | HG01109.hp2 HG02559.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1066-726dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901272 | ||||||
chr9:124901272
|
AT | A | 66 | a0001c0001t0003g0086a0002c0002t0001g0002a0002c0002t0001g0023others(63): Show | 76 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1066-726delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901272 | ||||||
chr9:124901356
|
C | T | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1066-809G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901356 | ||||||
chr9:124901419
|
C | T | 137 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0023others(134): Show | 158 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1066-872G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901419 | ||||||
chr9:124901428
|
G | A | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1066-881C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901428 | ||||||
chr9:124901436
|
A | AT | 93 | a0001c0001t0002g0123a0001c0001t0002g0128a0001c0001t0002g0129others(90): Show | 108 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1066-890dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901436 | ||||||
chr9:124901436
|
A | ATT | 53 | a0001c0001t0002g0205a0001c0001t0003g0082a0002c0002t0001g0265others(50): Show | 59 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1066-891_1066-890d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901436 | ||||||
chr9:124901492
|
T | C | 1 | a0002c0002t0001g0314 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1066-945A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901492 | ||||||
chr9:124901521
|
A | G | 13 | a0001c0001t0002g0006a0001c0001t0002g0066a0001c0001t0002g0067others(10): Show | 14 | HG00099.hp2 HG00597.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-974T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901521 | ||||||
chr9:124901523
|
C | T | 3 | a0002c0002t0001g0280a0002c0002t0001g0330a0012c0017t0004g0055 | 3 | HG02132.hp1 HG02683.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1066-976G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901523 | ||||||
chr9:124901547
|
A | G | 13 | a0001c0001t0002g0006a0001c0001t0002g0066a0001c0001t0002g0067others(10): Show | 14 | HG00099.hp2 HG00597.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-1000T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901547 | ||||||
chr9:124901567
|
TA | T | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1066-1021delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901567 | ||||||
chr9:124901605
|
T | A | 1 | a0003c0004t0006g0248 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1066-1058A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901605 | ||||||
chr9:124901687
|
G | C | 48 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(45): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1066-1140C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901687 | ||||||
chr9:124901757
|
G | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1066-1210C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124901757 | ||||||
chr9:124902134
|
T | C | 323 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(320): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1066-1587A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902134 | ||||||
chr9:124902180
|
C | T | 2 | a0003c0004t0013g0040a0011c0015t0013g0039 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1066-1633G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902180 | ||||||
chr9:124902317
|
T | C | 1 | a0002c0003t0001g0201 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1066-1770A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902317 | ||||||
chr9:124902402
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1066-1855C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902402 | ||||||
chr9:124902556
|
G | A | 4 | a0003c0004t0009g0038a0003c0004t0009g0058a0003c0004t0009g0060others(1): Show | 4 | HG00639.hp2 HG01884.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-2009C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902556 | ||||||
chr9:124902590
|
C | T | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1066-2043G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902590 | ||||||
chr9:124902634
|
C | T | 102 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(99): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1066-2087G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902634 | ||||||
chr9:124902690
|
C | T | 16 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(13): Show | 20 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.1066-2143G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902690 | ||||||
chr9:124902732
|
G | A | 1 | a0002c0002t0001g0282 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1066-2185C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902732 | ||||||
chr9:124902883
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1066-2336G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902883 | ||||||
chr9:124902906
|
A | G | 2 | a0002c0002t0001g0292a0002c0002t0001g0302 | 2 | NA18952.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1066-2359T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902906 | ||||||
chr9:124902951
|
C | T | 1 | a0002c0003t0001g0213 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1066-2404G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124902951 | ||||||
chr9:124903016
|
G | C | 7 | a0002c0002t0001g0004a0002c0002t0001g0308a0002c0002t0001g0309others(4): Show | 9 | HG00438.hp2 HG02129.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1066-2469C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903016 | ||||||
chr9:124903055
|
T | C | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | NA19000.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1066-2508A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903055 | ||||||
chr9:124903151
|
T | C | 49 | a0001c0001t0002g0205a0002c0003t0001g0001a0002c0003t0001g0017others(46): Show | 55 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1066-2604A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903151 | ||||||
chr9:124903179
|
G | A | 1 | a0002c0003t0001g0213 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1066-2632C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903179 | ||||||
chr9:124903180
|
C | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1066-2633G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903180 | ||||||
chr9:124903186
|
T | C | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1066-2639A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903186 | ||||||
chr9:124903187
|
C | A | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1066-2640G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903187 | ||||||
chr9:124903188
|
C | A | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1066-2641G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903188 | ||||||
chr9:124903594
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1066-3047C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903594 | ||||||
chr9:124903651
|
C | CA | 84 | a0001c0001t0003g0047a0001c0001t0008g0035a0001c0005t0005g0005others(81): Show | 102 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.1066-3105dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903651 | ||||||
chr9:124903651
|
C | CAA | 13 | a0002c0002t0001g0251a0002c0002t0001g0256a0002c0002t0001g0264others(10): Show | 13 | HG00423.hp2 HG00438.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1066-3106_1066-310 others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903651 | ||||||
chr9:124903651
|
CA | C | 206 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(203): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1066-3105delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903651 | ||||||
chr9:124903792
|
T | C | 13 | a0001c0001t0002g0006a0001c0001t0002g0066a0001c0001t0002g0067others(10): Show | 14 | HG00099.hp2 HG00597.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066-3245A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903792 | ||||||
chr9:124903817
|
G | A | 1 | a0001c0001t0002g0072 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1066-3270C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903817 | ||||||
chr9:124903862
|
A | G | 104 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(101): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1066-3315T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124903862 | ||||||
chr9:124904072
|
TA | T | 54 | a0001c0001t0002g0123a0001c0001t0002g0205a0001c0001t0003g0082others(51): Show | 60 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1066-3526delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904072 | ||||||
chr9:124904090
|
T | G | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1066-3543A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904090 | ||||||
chr9:124904093
|
TA | T | 51 | a0001c0001t0002g0123a0001c0001t0003g0007a0001c0001t0003g0008others(48): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1066-3547delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904093 | ||||||
chr9:124904154
|
T | C | 43 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(40): Show | 47 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.1066-3607A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904154 | ||||||
chr9:124904248
|
G | A | 2 | a0003c0004t0013g0040a0011c0015t0013g0039 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1066-3701C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904248 | ||||||
chr9:124904256
|
A | G | 6 | a0002c0002t0001g0004a0002c0002t0001g0320a0002c0002t0001g0321others(3): Show | 8 | HG00438.hp2 HG02080.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1066-3709T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904256 | ||||||
chr9:124904637
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1065+3740G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904637 | ||||||
chr9:124904668
|
G | A | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1065+3709C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904668 | ||||||
chr9:124904677
|
C | T | 1 | a0001c0001t0017g0240 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1065+3700G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904677 | ||||||
chr9:124904756
|
A | G | 64 | a0001c0001t0002g0205a0001c0001t0016g0041a0002c0003t0001g0001others(61): Show | 70 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1065+3621T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904756 | ||||||
chr9:124904788
|
A | C | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065+3589T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904788 | ||||||
chr9:124904877
|
G | A | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065+3500C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904877 | ||||||
chr9:124904897
|
T | C | 8 | a0001c0001t0002g0117a0001c0001t0002g0124a0001c0001t0002g0125others(5): Show | 8 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065+3480A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904897 | ||||||
chr9:124904927
|
G | C | 108 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(105): Show | 116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1065+3450C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904927 | ||||||
chr9:124904943
|
C | CA | 310 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(307): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1065+3433dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904943 | ||||||
chr9:124904954
|
A | AT | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0128others(6): Show | 11 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1065+3422_1065+342 others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904954 | ||||||
chr9:124904956
|
T | A | 16 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0020others(13): Show | 19 | HG00733.hp2 HG00741.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1065+3421A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904956 | ||||||
chr9:124904992
|
A | C | 1 | a0001c0001t0002g0154 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1065+3385T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124904992 | ||||||
chr9:124905149
|
AAAT | A | 86 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0023others(83): Show | 101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1065+3225_1065+322 others(7): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905149 | ||||||
chr9:124905415
|
T | C | 2 | a0002c0002t0001g0319a0002c0002t0001g0326 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1065+2962A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905415 | ||||||
chr9:124905649
|
T | C | 1 | a0002c0002t0001g0283 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1065+2728A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905649 | ||||||
chr9:124905890
|
C | T | 1 | a0001c0001t0004g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1065+2487G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905890 | ||||||
chr9:124905965
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1065+2412A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905965 | ||||||
chr9:124905972
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1065+2405C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905972 | ||||||
chr9:124905973
|
C | T | 1 | a0002c0002t0001g0259 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1065+2404G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905973 | ||||||
chr9:124905994
|
T | C | 2 | a0002c0003t0012g0113a0002c0003t0012g0114 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1065+2383A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124905994 | ||||||
chr9:124906116
|
A | AAAAT | 9 | a0001c0001t0004g0022a0001c0001t0004g0241a0001c0001t0004g0242others(6): Show | 10 | HG01123.hp1 HG01255.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1065+2257_1065+226 others(8): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | ||||||
chr9:124906116
|
A | AAAATAAA others(1): Show |
19 | a0001c0001t0004g0233a0001c0001t0016g0041a0002c0002t0001g0256others(16): Show | 20 | HG00733.hp1 HG01081.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.1065+2253_1065+226 others(12): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | ||||||
chr9:124906116
|
A | AAAATAAA others(5): Show |
92 | a0002c0002t0001g0002a0002c0002t0001g0023a0002c0002t0001g0024others(89): Show | 110 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1065+2249_1065+226 others(16): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | ||||||
chr9:124906116
|
A | AAAATAAA others(9): Show |
23 | a0002c0002t0001g0004a0002c0002t0001g0253a0002c0002t0001g0258others(20): Show | 25 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1065+2245_1065+226 others(20): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | ||||||
chr9:124906116
|
AAAAT | A | 171 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(168): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1065+2257_1065+226 others(8): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906116 | ||||||
chr9:124906262
|
C | T | 1 | a0002c0003t0001g0199 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1065+2115G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906262 | ||||||
chr9:124906305
|
C | T | 1 | a0002c0002t0001g0251 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1065+2072G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906305 | ||||||
chr9:124906345
|
C | T | 9 | a0002c0003t0001g0188a0002c0003t0001g0189a0002c0003t0001g0197others(6): Show | 9 | HG02027.hp2 NA18943.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1065+2032G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906345 | ||||||
chr9:124906419
|
A | G | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG01975.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1065+1958T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906419 | ||||||
chr9:124906425
|
T | C | 323 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(320): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1065+1952A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906425 | ||||||
chr9:124906461
|
C | G | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1065+1916G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906461 | ||||||
chr9:124906526
|
G | C | 1 | a0001c0001t0002g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1065+1851C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906526 | ||||||
chr9:124906612
|
C | T | 167 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(164): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1065+1765G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124906612 | ||||||
chr9:124907194
|
A | T | 1 | a0002c0003t0001g0227 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1065+1183T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907194 | ||||||
chr9:124907204
|
A | G | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1065+1173T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907204 | ||||||
chr9:124907255
|
A | G | 149 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(146): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1065+1122T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907255 | ||||||
chr9:124907556
|
G | C | 6 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(3): Show | 6 | HG01069.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065+821C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907556 | ||||||
chr9:124907724
|
T | C | 1 | a0002c0002t0001g0259 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1065+653A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907724 | ||||||
chr9:124907737
|
T | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1065+640A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907737 | ||||||
chr9:124907758
|
C | G | 144 | a0001c0001t0002g0299a0001c0001t0008g0035a0002c0002t0001g0002others(141): Show | 165 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1065+619G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907758 | ||||||
chr9:124907822
|
G | T | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065+555C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907822 | ||||||
chr9:124907871
|
G | A | 1 | a0002c0002t0001g0303 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1065+506C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124907871 | ||||||
chr9:124908098
|
A | G | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1065+279T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124908098 | ||||||
chr9:124908099
|
A | G | 323 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(320): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1065+278T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124908099 | ||||||
chr9:124908294
|
C | T | 1 | a0004c0007t0007g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1065+83G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 12/22 | chr9 | 124908294 | ||||||
chr9:124908527
|
T | A | 1 | a0002c0003t0001g0227 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.970-55A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908527 | ||||||
chr9:124908668
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.970-196T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908668 | ||||||
chr9:124908743
|
G | A | 91 | a0001c0001t0002g0299a0002c0002t0001g0002a0002c0002t0001g0004others(88): Show | 106 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.970-271C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908743 | ||||||
chr9:124908757
|
C | T | 2 | a0002c0003t0012g0113a0002c0003t0012g0114 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.970-285G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908757 | ||||||
chr9:124908802
|
G | C | 1 | a0001c0001t0002g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.970-330C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908802 | ||||||
chr9:124908804
|
G | A | 1 | a0002c0002t0001g0300 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.970-332C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908804 | ||||||
chr9:124908850
|
C | T | 1 | a0002c0002t0001g0297 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.970-378G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908850 | ||||||
chr9:124908861
|
G | A | 162 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(159): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.970-389C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124908861 | ||||||
chr9:124909048
|
A | C | 51 | a0002c0003t0001g0001a0002c0003t0001g0017a0002c0003t0001g0018others(48): Show | 57 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.970-576T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909048 | ||||||
chr9:124909120
|
G | A | 1 | a0003c0004t0006g0248 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.970-648C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909120 | ||||||
chr9:124909146
|
C | T | 3 | a0002c0002t0001g0029a0002c0002t0001g0313a0002c0002t0001g0314 | 4 | HG00140.hp2 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.970-674G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909146 | ||||||
chr9:124909311
|
T | TA | 15 | a0001c0001t0003g0099a0002c0002t0001g0026a0002c0002t0001g0028others(12): Show | 18 | HG00673.hp1 HG02040.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.970-840dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909311 | ||||||
chr9:124909311
|
TA | T | 9 | a0001c0001t0003g0080a0002c0003t0001g0188a0002c0003t0001g0189others(6): Show | 9 | HG02027.hp2 NA18943.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.970-840delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909311 | ||||||
chr9:124909373
|
C | T | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.970-901G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909373 | ||||||
chr9:124909608
|
C | CA | 7 | a0001c0001t0002g0166a0001c0001t0002g0173a0001c0001t0003g0082others(4): Show | 7 | HG01981.hp2 HG02074.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.970-1137dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909608 | ||||||
chr9:124909608
|
C | CAAA | 10 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(7): Show | 10 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.970-1139_970-1137d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909608 | ||||||
chr9:124909608
|
CA | C | 132 | a0001c0001t0002g0066a0001c0001t0002g0179a0002c0002t0001g0002others(129): Show | 153 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.970-1137delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909608 | ||||||
chr9:124909608
|
CAA | C | 9 | a0002c0002t0001g0262a0002c0003t0001g0194a0002c0003t0001g0196others(6): Show | 9 | HG00558.hp1 HG00609.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.970-1138_970-1137d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909608 | ||||||
chr9:124909625
|
A | G | 4 | a0001c0001t0002g0123a0001c0001t0002g0158a0001c0001t0002g0159others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.970-1153T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909625 | ||||||
chr9:124909734
|
G | C | 1 | a0001c0001t0002g0140 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.970-1262C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909734 | ||||||
chr9:124909804
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0176 | 3 | NA18970.hp2 NA18989.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.970-1332C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909804 | ||||||
chr9:124909870
|
T | C | 166 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.970-1398A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909870 | ||||||
chr9:124909898
|
G | A | 90 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0023others(87): Show | 105 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.970-1426C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909898 | ||||||
chr9:124909968
|
G | A | 1 | a0002c0002t0001g0297 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.970-1496C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124909968 | ||||||
chr9:124910146
|
G | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.970-1674C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910146 | ||||||
chr9:124910319
|
C | A | 103 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.969+1582G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910319 | ||||||
chr9:124910501
|
T | C | 1 | a0002c0002t0001g0304 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.969+1400A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910501 | ||||||
chr9:124910583
|
T | C | 1 | a0002c0002t0001g0284 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.969+1318A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910583 | ||||||
chr9:124910939
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.969+962G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910939 | ||||||
chr9:124910953
|
C | G | 323 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(320): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.969+948G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910953 | ||||||
chr9:124910999
|
C | A | 1 | a0002c0003t0001g0228 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.969+902G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124910999 | ||||||
chr9:124911046
|
T | C | 2 | a0001c0001t0003g0009a0001c0001t0003g0086 | 3 | NA18955.hp1 NA18962.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.969+855A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911046 | ||||||
chr9:124911106
|
A | C | 166 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.969+795T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911106 | ||||||
chr9:124911190
|
C | T | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.969+711G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911190 | ||||||
chr9:124911210
|
C | G | 1 | a0001c0001t0002g0140 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.969+691G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911210 | ||||||
chr9:124911321
|
G | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.969+580C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911321 | ||||||
chr9:124911518
|
G | A | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.969+383C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911518 | ||||||
chr9:124911598
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.969+303G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911598 | ||||||
chr9:124911670
|
C | T | 163 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(160): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.969+231G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911670 | ||||||
chr9:124911697
|
CT | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.969+203delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911697 | ||||||
chr9:124911725
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.969+176G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911725 | ||||||
chr9:124911761
|
G | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.969+140C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911761 | ||||||
chr9:124911812
|
C | G | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.969+89G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911812 | ||||||
chr9:124911870
|
C | T | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+31G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 11/22 | chr9 | 124911870 | ||||||
chr9:124912110
|
T | C | 1 | a0002c0002t0001g0323 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.844-84A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912110 | ||||||
chr9:124912552
|
T | G | 1 | a0001c0001t0010g0247 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.844-526A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912552 | ||||||
chr9:124912554
|
G | T | 1 | a0001c0001t0010g0247 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.844-528C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912554 | ||||||
chr9:124912566
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.844-540C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912566 | ||||||
chr9:124912575
|
C | G | 1 | a0001c0001t0002g0020 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.844-549G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912575 | ||||||
chr9:124912605
|
C | T | 48 | a0002c0003t0001g0001a0002c0003t0001g0017a0002c0003t0001g0018others(45): Show | 54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.844-579G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912605 | ||||||
chr9:124912606
|
G | A | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-580C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912606 | ||||||
chr9:124912667
|
C | T | 22 | a0001c0001t0002g0015a0001c0001t0002g0161a0001c0001t0002g0168others(19): Show | 23 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-641G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912667 | ||||||
chr9:124912845
|
C | CT | 10 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(7): Show | 10 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.844-820dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124912845 | ||||||
chr9:124913093
|
G | A | 1 | a0002c0002t0001g0297 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.844-1067C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913093 | ||||||
chr9:124913246
|
G | A | 1 | a0003c0004t0013g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.844-1220C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913246 | ||||||
chr9:124913299
|
T | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-1273A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913299 | ||||||
chr9:124913385
|
G | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-1359C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913385 | ||||||
chr9:124913514
|
G | C | 1 | a0003c0004t0006g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.844-1488C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913514 | ||||||
chr9:124913541
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.844-1515T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913541 | ||||||
chr9:124913542
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.844-1516G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913542 | ||||||
chr9:124913596
|
G | A | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-1570C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913596 | ||||||
chr9:124913613
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.844-1587T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913613 | ||||||
chr9:124913750
|
C | A | 329 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.844-1724G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124913750 | ||||||
chr9:124914054
|
T | G | 3 | a0002c0003t0001g0229a0002c0003t0001g0230a0002c0003t0001g0231 | 3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.844-2028A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914054 | ||||||
chr9:124914154
|
G | A | 2 | a0001c0005t0005g0033a0001c0005t0005g0333 | 3 | HG02451.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.844-2128C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914154 | ||||||
chr9:124914255
|
T | C | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.844-2229A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914255 | ||||||
chr9:124914546
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.844-2520C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914546 | ||||||
chr9:124914635
|
G | C | 1 | a0001c0001t0003g0093 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.844-2609C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914635 | ||||||
chr9:124914639
|
G | A | 14 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0120others(11): Show | 16 | HG00280.hp2 HG01074.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.844-2613C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914639 | ||||||
chr9:124914953
|
T | C | 93 | a0001c0001t0002g0299a0001c0001t0008g0035a0002c0002t0001g0002others(90): Show | 108 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.844-2927A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914953 | ||||||
chr9:124914995
|
G | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.844-2969C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124914995 | ||||||
chr9:124915027
|
A | T | 1 | a0002c0002t0001g0024 | 2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.844-3001T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915027 | ||||||
chr9:124915121
|
T | C | 5 | a0002c0002t0001g0258a0002c0002t0001g0284a0002c0002t0001g0294others(2): Show | 5 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-3095A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915121 | ||||||
chr9:124915319
|
G | A | 53 | a0001c0001t0002g0205a0001c0001t0016g0041a0002c0003t0001g0001others(50): Show | 59 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.844-3293C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915319 | ||||||
chr9:124915522
|
T | C | 2 | a0001c0001t0002g0112a0001c0001t0002g0118 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.844-3496A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915522 | ||||||
chr9:124915639
|
C | T | 29 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0115others(26): Show | 31 | HG00280.hp2 HG00423.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.844-3613G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915639 | ||||||
chr9:124915733
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.844-3707G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915733 | ||||||
chr9:124915742
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.844-3716C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915742 | ||||||
chr9:124915873
|
G | A | 1 | a0001c0001t0017g0240 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.844-3847C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124915873 | ||||||
chr9:124916012
|
G | T | 2 | a0002c0002t0011g0030a0002c0002t0011g0315 | 3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844-3986C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916012 | ||||||
chr9:124916101
|
C | CTAAA | 106 | a0001c0001t0002g0112a0001c0001t0002g0118a0001c0001t0002g0187others(103): Show | 125 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.844-4079_844-4076d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916101 | ||||||
chr9:124916101
|
C | CTAAATAA others(1): Show |
11 | a0001c0001t0004g0239a0002c0002t0001g0317a0002c0003t0001g0188others(8): Show | 11 | HG02027.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.844-4083_844-4076d others(10): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916101 | ||||||
chr9:124916101
|
C | CTAAATAA others(5): Show |
26 | a0001c0001t0016g0041a0001c0001t0017g0240a0002c0003t0001g0001others(23): Show | 30 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.844-4087_844-4076d others(14): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916101 | ||||||
chr9:124916101
|
C | CTAAATAA others(9): Show |
19 | a0001c0001t0002g0205a0002c0002t0001g0263a0002c0003t0001g0018others(16): Show | 21 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-4091_844-4076d others(18): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916101 | ||||||
chr9:124916120
|
A | C | 7 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0056others(4): Show | 9 | NA18955.hp1 NA18960.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-4094T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916120 | ||||||
chr9:124916124
|
A | AATAAATA others(5): Show |
1 | a0002c0003t0001g0190 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.844-4099_844-4098i others(14): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916124 | ||||||
chr9:124916128
|
A | AATAAATA others(5): Show |
1 | a0002c0003t0014g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844-4103_844-4102i others(14): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916128 | ||||||
chr9:124916178
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.844-4152G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916178 | ||||||
chr9:124916399
|
T | G | 1 | a0002c0002t0001g0256 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.844-4373A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916399 | ||||||
chr9:124916600
|
A | G | 2 | a0002c0002t0001g0280a0002c0002t0001g0330 | 2 | HG02132.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.843+4529T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916600 | ||||||
chr9:124916652
|
T | C | 14 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0020others(11): Show | 17 | HG00733.hp2 HG00741.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+4477A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916652 | ||||||
chr9:124916715
|
A | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0118 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.843+4414T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916715 | ||||||
chr9:124916867
|
C | T | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.843+4262G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916867 | ||||||
chr9:124916871
|
G | GAC | 4 | a0002c0003t0001g0019a0002c0003t0001g0192a0002c0003t0001g0229others(1): Show | 5 | HG03130.hp2 NA18906.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+4256_843+4257d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916871 | ||||||
chr9:124916877
|
C | CA | 141 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0013others(138): Show | 157 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.843+4251dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916877 | ||||||
chr9:124916877
|
C | CAA | 50 | a0001c0001t0002g0057a0001c0001t0002g0067a0001c0001t0002g0068others(47): Show | 58 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.843+4250_843+4251d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916877 | ||||||
chr9:124916878
|
A | AC | 23 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0046others(20): Show | 24 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.843+4250_843+4251i others(3): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916878 | ||||||
chr9:124916879
|
A | C | 35 | a0001c0001t0002g0139a0001c0001t0002g0160a0001c0001t0003g0007others(32): Show | 39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+4250T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916879 | ||||||
chr9:124916880
|
A | C | 17 | a0001c0001t0003g0043a0001c0001t0003g0046a0001c0001t0003g0049others(14): Show | 17 | HG00738.hp1 HG01167.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+4249T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916880 | ||||||
chr9:124916881
|
A | C | 30 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(27): Show | 34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.843+4248T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916881 | ||||||
chr9:124916882
|
A | C | 1 | a0001c0001t0003g0087 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.843+4247T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916882 | ||||||
chr9:124916883
|
A | C | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0056others(2): Show | 7 | NA18955.hp1 NA18960.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.843+4246T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916883 | ||||||
chr9:124916909
|
C | CA | 9 | a0001c0001t0003g0046a0001c0001t0003g0080a0001c0001t0003g0081others(6): Show | 9 | HG03654.hp1 NA18944.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+4219dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124916909 | ||||||
chr9:124917295
|
C | A | 1 | a0002c0002t0001g0301 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.843+3834G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917295 | ||||||
chr9:124917535
|
CATT | C | 5 | a0001c0001t0002g0014a0001c0001t0002g0119a0001c0001t0002g0163others(2): Show | 6 | HG02055.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+3591_843+3593d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917535 | ||||||
chr9:124917581
|
C | T | 5 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+3548G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917581 | ||||||
chr9:124917762
|
C | T | 1 | a0002c0002t0001g0279 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.843+3367G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917762 | ||||||
chr9:124917856
|
T | C | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.843+3273A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917856 | ||||||
chr9:124917857
|
A | T | 47 | a0001c0001t0002g0205a0002c0003t0001g0001a0002c0003t0001g0017others(44): Show | 53 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.843+3272T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917857 | ||||||
chr9:124917859
|
A | T | 50 | a0001c0001t0002g0205a0002c0002t0001g0277a0002c0003t0001g0001others(47): Show | 56 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.843+3270T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917859 | ||||||
chr9:124917860
|
T | TA | 3 | a0001c0005t0005g0332a0002c0002t0001g0253a0002c0003t0001g0037 | 3 | HG02145.hp1 HG02723.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.843+3268_843+3269i others(3): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917860 | ||||||
chr9:124917861
|
T | A | 185 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(182): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.843+3268A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917861 | ||||||
chr9:124917863
|
T | A | 8 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0249others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.843+3266A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124917863 | ||||||
chr9:124918066
|
G | A | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.843+3063C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918066 | ||||||
chr9:124918072
|
G | A | 1 | a0002c0002t0001g0271 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.843+3057C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918072 | ||||||
chr9:124918146
|
C | T | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+2983G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918146 | ||||||
chr9:124918160
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.843+2969T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918160 | ||||||
chr9:124918226
|
T | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+2903A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918226 | ||||||
chr9:124918746
|
A | T | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.843+2383T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918746 | ||||||
chr9:124918875
|
T | G | 167 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(164): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.843+2254A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918875 | ||||||
chr9:124918886
|
G | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+2243C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124918886 | ||||||
chr9:124919015
|
G | C | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.843+2114C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919015 | ||||||
chr9:124919066
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.843+2063A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919066 | ||||||
chr9:124919132
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.843+1997G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919132 | ||||||
chr9:124919232
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0233a0001c0001t0004g0241others(1): Show | 5 | HG01123.hp1 HG01255.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+1897C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919232 | ||||||
chr9:124919262
|
A | G | 1 | a0002c0002t0001g0260 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.843+1867T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919262 | ||||||
chr9:124919705
|
A | T | 193 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(190): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.843+1424T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919705 | ||||||
chr9:124919719
|
G | A | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+1410C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919719 | ||||||
chr9:124919740
|
C | T | 2 | a0001c0001t0003g0050a0001c0001t0003g0085 | 2 | HG02135.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.843+1389G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919740 | ||||||
chr9:124919936
|
A | ATATT | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+1189_843+1192d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919936 | ||||||
chr9:124919936
|
A | T | 1 | a0001c0001t0002g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.843+1193T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919936 | ||||||
chr9:124919936
|
ATATT | A | 8 | a0002c0003t0001g0018a0002c0003t0001g0191a0002c0003t0001g0194others(5): Show | 9 | HG00558.hp1 HG00597.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+1189_843+1192d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919936 | ||||||
chr9:124919978
|
CAG | C | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+1149_843+1150d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919978 | ||||||
chr9:124919981
|
A | G | 2 | a0001c0001t0002g0128a0001c0001t0002g0129 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.843+1148T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124919981 | ||||||
chr9:124920007
|
T | A | 1 | a0001c0001t0002g0299 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.843+1122A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920007 | ||||||
chr9:124920013
|
G | A | 1 | a0001c0001t0019g0136 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.843+1116C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920013 | ||||||
chr9:124920090
|
A | AG | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.843+1038_843+1039i others(3): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920090 | ||||||
chr9:124920286
|
AT | A | 57 | a0001c0001t0002g0129a0001c0001t0002g0137a0001c0001t0002g0205others(54): Show | 63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.843+842delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920286 | ||||||
chr9:124920308
|
G | A | 2 | a0002c0002t0001g0310a0002c0002t0001g0311 | 2 | NA18945.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.843+821C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920308 | ||||||
chr9:124920332
|
CAT | C | 144 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(141): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.843+795_843+796del others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920332 | ||||||
chr9:124920434
|
T | C | 1 | a0002c0002t0001g0264 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.843+695A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920434 | ||||||
chr9:124920659
|
G | C | 4 | a0002c0002t0001g0025a0002c0002t0001g0032a0002c0002t0001g0271others(1): Show | 6 | HG01099.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+470C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920659 | ||||||
chr9:124920680
|
A | C | 2 | a0002c0003t0012g0113a0002c0003t0012g0114 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.843+449T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920680 | ||||||
chr9:124920751
|
T | C | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.843+378A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920751 | ||||||
chr9:124920855
|
G | GA | 55 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0020others(52): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.843+273dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920855 | ||||||
chr9:124920855
|
GA | G | 56 | a0001c0001t0002g0076a0001c0001t0002g0123a0001c0001t0002g0158others(53): Show | 62 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.843+273delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124920855 | ||||||
chr9:124921035
|
G | T | 1 | a0002c0002t0001g0278 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.843+94C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124921035 | ||||||
chr9:124921105
|
G | A | 2 | a0003c0004t0013g0040a0011c0015t0013g0039 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.843+24C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 10/22 | chr9 | 124921105 | ||||||
chr9:124921373
|
C | T | 2 | a0001c0001t0003g0046a0001c0001t0003g0083 | 2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.732-133G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/22 | chr9 | 124921373 | ||||||
chr9:124921497
|
G | C | 1 | a0002c0003t0001g0223 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.731+226C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/22 | chr9 | 124921497 | ||||||
chr9:124921619
|
C | T | 1 | a0002c0002t0001g0277 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.731+104G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 9/22 | chr9 | 124921619 | ||||||
chr9:124921976
|
C | T | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-84G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124921976 | ||||||
chr9:124921993
|
T | G | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.562-101A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124921993 | ||||||
chr9:124922044
|
A | G | 1 | a0002c0003t0001g0194 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.562-152T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922044 | ||||||
chr9:124922153
|
G | A | 1 | a0002c0003t0001g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.562-261C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922153 | ||||||
chr9:124922409
|
C | T | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-517G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922409 | ||||||
chr9:124922423
|
C | T | 2 | a0001c0001t0002g0067a0001c0001t0002g0071 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.562-531G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922423 | ||||||
chr9:124922550
|
C | CA | 6 | a0001c0001t0002g0127a0001c0001t0003g0101a0001c0001t0004g0242others(3): Show | 6 | HG01257.hp2 HG03831.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+544dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922550 | ||||||
chr9:124922861
|
A | C | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | NA19055.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.561+234T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922861 | ||||||
chr9:124922884
|
C | G | 7 | a0002c0002t0001g0002a0002c0002t0001g0253a0002c0002t0001g0259others(4): Show | 10 | NA18954.hp2 NA18957.hp2 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.561+211G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124922884 | ||||||
chr9:124923014
|
G | T | 4 | a0003c0004t0009g0038a0003c0004t0009g0058a0003c0004t0009g0060others(1): Show | 4 | HG00639.hp2 HG01884.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+81C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 8/22 | chr9 | 124923014 | ||||||
chr9:124923227
|
T | C | 24 | a0001c0001t0002g0015a0001c0001t0002g0168a0001c0001t0002g0169others(21): Show | 25 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.433-4A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923227 | ||||||
chr9:124923231
|
A | G | 53 | a0001c0001t0002g0205a0001c0001t0016g0041a0002c0003t0001g0001others(50): Show | 59 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
splice_region_variant&intron_variant | LOW | c.433-8T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923231 | ||||||
chr9:124923237
|
G | A | 2 | a0002c0002t0001g0300a0002c0002t0001g0324 | 2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.433-14C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923237 | ||||||
chr9:124923282
|
G | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-59C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923282 | ||||||
chr9:124923383
|
C | T | 5 | a0002c0002t0001g0031a0002c0002t0001g0267a0002c0002t0001g0316others(2): Show | 6 | HG02622.hp1 HG02886.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-160G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923383 | ||||||
chr9:124923537
|
T | C | 2 | a0001c0001t0002g0112a0001c0001t0002g0118 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.433-314A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923537 | ||||||
chr9:124923662
|
T | C | 1 | a0002c0002t0001g0325 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.433-439A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923662 | ||||||
chr9:124923781
|
G | A | 10 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(7): Show | 13 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.433-558C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923781 | ||||||
chr9:124923847
|
C | T | 248 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(245): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.433-624G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124923847 | ||||||
chr9:124924136
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.433-913C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924136 | ||||||
chr9:124924370
|
C | T | 1 | a0001c0001t0004g0232 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.433-1147G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924370 | ||||||
chr9:124924440
|
C | T | 101 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0013others(98): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.433-1217G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924440 | ||||||
chr9:124924636
|
C | CA | 221 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(218): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.433-1414dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924636 | ||||||
chr9:124924636
|
C | CAA | 21 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0020others(18): Show | 27 | HG00597.hp2 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.433-1415_433-1414d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924636 | ||||||
chr9:124924655
|
A | T | 1 | a0002c0002t0020g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.433-1432T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924655 | ||||||
chr9:124924691
|
C | T | 9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0128others(6): Show | 11 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-1468G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924691 | ||||||
chr9:124924756
|
G | T | 5 | a0002c0002t0001g0031a0002c0002t0001g0267a0002c0002t0001g0316others(2): Show | 6 | HG02622.hp1 HG02886.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-1533C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924756 | ||||||
chr9:124924921
|
T | C | 3 | a0001c0001t0002g0112a0001c0001t0002g0118a0001c0001t0002g0249 | 3 | HG01109.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.433-1698A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924921 | ||||||
chr9:124924932
|
T | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0155a0001c0001t0002g0156others(1): Show | 5 | HG01106.hp1 HG01123.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-1709A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124924932 | ||||||
chr9:124925103
|
C | T | 1 | a0002c0002t0001g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.432+1606G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925103 | ||||||
chr9:124925156
|
T | G | 3 | a0001c0001t0002g0112a0001c0001t0002g0118a0001c0001t0002g0249 | 3 | HG01109.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.432+1553A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925156 | ||||||
chr9:124925221
|
AT | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.432+1487delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925221 | ||||||
chr9:124925285
|
T | C | 23 | a0001c0001t0002g0015a0001c0001t0002g0168a0001c0001t0002g0169others(20): Show | 24 | HG00408.hp1 HG00609.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.432+1424A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925285 | ||||||
chr9:124925359
|
AT | A | 191 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(188): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.432+1349delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925359 | ||||||
chr9:124925359
|
ATT | A | 50 | a0001c0001t0002g0205a0001c0001t0003g0050a0002c0003t0001g0001others(47): Show | 55 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.432+1348_432+1349d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925359 | ||||||
chr9:124925457
|
C | T | 2 | a0003c0004t0013g0040a0011c0015t0013g0039 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.432+1252G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925457 | ||||||
chr9:124925735
|
C | T | 48 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(45): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.432+974G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925735 | ||||||
chr9:124925937
|
T | C | 4 | a0001c0001t0002g0133a0001c0001t0002g0134a0001c0001t0002g0135others(1): Show | 4 | HG01175.hp2 HG01952.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+772A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124925937 | ||||||
chr9:124926148
|
G | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.432+561C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926148 | ||||||
chr9:124926174
|
A | G | 4 | a0004c0007t0007g0051a0004c0007t0007g0052a0004c0007t0007g0053others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+535T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926174 | ||||||
chr9:124926265
|
C | T | 1 | a0003c0004t0009g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.432+444G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926265 | ||||||
chr9:124926267
|
A | G | 46 | a0001c0001t0002g0205a0002c0003t0001g0001a0002c0003t0001g0017others(43): Show | 51 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.432+442T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926267 | ||||||
chr9:124926335
|
A | G | 39 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0115others(36): Show | 41 | HG00280.hp2 HG00423.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.432+374T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926335 | ||||||
chr9:124926398
|
A | G | 2 | a0001c0001t0002g0069a0001c0010t0002g0070 | 2 | NA18942.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.432+311T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926398 | ||||||
chr9:124926415
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.432+294C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926415 | ||||||
chr9:124926688
|
C | T | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.432+21G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 7/22 | chr9 | 124926688 | ||||||
chr9:124926890
|
G | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.400-149C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124926890 | ||||||
chr9:124927040
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.400-299G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927040 | ||||||
chr9:124927249
|
G | A | 1 | a0002c0002t0001g0302 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.400-508C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927249 | ||||||
chr9:124927348
|
G | T | 2 | a0002c0003t0001g0227a0002c0003t0001g0228 | 2 | NA19054.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.400-607C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927348 | ||||||
chr9:124927375
|
C | A | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.400-634G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927375 | ||||||
chr9:124927407
|
T | C | 2 | a0002c0003t0001g0227a0002c0003t0001g0228 | 2 | NA19054.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.400-666A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927407 | ||||||
chr9:124927442
|
A | T | 1 | a0002c0002t0001g0269 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.400-701T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927442 | ||||||
chr9:124927540
|
ACT | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0171a0001c0001t0002g0172others(5): Show | 9 | HG00609.hp2 HG02074.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+646_399+647del others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927540 | ||||||
chr9:124927632
|
T | C | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+556A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927632 | ||||||
chr9:124927709
|
G | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+479C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927709 | ||||||
chr9:124927876
|
T | C | 1 | a0001c0001t0002g0184 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.399+312A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124927876 | ||||||
chr9:124928005
|
A | T | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.399+183T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124928005 | ||||||
chr9:124928050
|
A | C | 1 | a0002c0003t0001g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.399+138T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 6/22 | chr9 | 124928050 | ||||||
chr9:124928332
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.302-47G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928332 | ||||||
chr9:124928523
|
T | C | 1 | a0002c0002t0001g0303 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.302-238A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928523 | ||||||
chr9:124928546
|
GT | G | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.302-262delA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928546 | ||||||
chr9:124928643
|
A | G | 1 | a0001c0001t0003g0081 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.302-358T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928643 | ||||||
chr9:124928773
|
T | C | 1 | a0002c0002t0001g0304 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.301+443A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928773 | ||||||
chr9:124928840
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.301+376T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928840 | ||||||
chr9:124928905
|
T | TCCAGACC others(111): Show |
1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.301+193_301+310dup others(118): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124928905 | ||||||
chr9:124929090
|
A | T | 1 | a0001c0001t0002g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.301+126T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 5/22 | chr9 | 124929090 | ||||||
chr9:124929524
|
GC | G | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.227-235delG | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929524 | ||||||
chr9:124929672
|
C | T | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.227-382G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929672 | ||||||
chr9:124929710
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.227-420G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929710 | ||||||
chr9:124929781
|
A | C | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.227-491T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929781 | ||||||
chr9:124929821
|
C | T | 1 | a0002c0003t0001g0191 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.227-531G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929821 | ||||||
chr9:124929959
|
T | C | 4 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(1): Show | 4 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-669A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124929959 | ||||||
chr9:124930152
|
C | T | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-862G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930152 | ||||||
chr9:124930167
|
C | T | 4 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(1): Show | 4 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-877G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930167 | ||||||
chr9:124930181
|
T | C | 5 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0098others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-891A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930181 | ||||||
chr9:124930259
|
C | A | 1 | a0001c0001t0003g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.227-969G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930259 | ||||||
chr9:124930322
|
A | G | 167 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(164): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.226+994T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930322 | ||||||
chr9:124930399
|
C | T | 1 | a0002c0002t0001g0264 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.226+917G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930399 | ||||||
chr9:124930558
|
T | C | 4 | a0002c0002t0001g0250a0002c0002t0001g0261a0002c0002t0001g0305others(1): Show | 4 | HG00558.hp2 NA18965.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+758A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930558 | ||||||
chr9:124930840
|
A | G | 1 | a0002c0003t0001g0190 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.226+476T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930840 | ||||||
chr9:124930969
|
T | C | 193 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(190): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.226+347A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124930969 | ||||||
chr9:124931021
|
A | G | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.226+295T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124931021 | ||||||
chr9:124931111
|
T | A | 1 | a0002c0002t0001g0307 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.226+205A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124931111 | ||||||
chr9:124931201
|
A | T | 1 | a0001c0001t0003g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.226+115T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 4/22 | chr9 | 124931201 | ||||||
chr9:124931428
|
A | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-22T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931428 | ||||||
chr9:124931568
|
C | T | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-162G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931568 | ||||||
chr9:124931596
|
G | C | 1 | a0001c0001t0003g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136-190C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931596 | ||||||
chr9:124931786
|
G | A | 1 | a0001c0001t0003g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136-380C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931786 | ||||||
chr9:124931850
|
C | T | 1 | a0002c0003t0014g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.136-444G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931850 | ||||||
chr9:124931930
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.136-524C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124931930 | ||||||
chr9:124932352
|
C | T | 52 | a0001c0001t0002g0205a0002c0003t0001g0001a0002c0003t0001g0017others(49): Show | 58 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.136-946G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932352 | ||||||
chr9:124932382
|
A | G | 1 | a0002c0003t0001g0268 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136-976T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932382 | ||||||
chr9:124932390
|
T | C | 2 | a0001c0001t0003g0100a0001c0001t0003g0101 | 2 | HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136-984A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932390 | ||||||
chr9:124932395
|
G | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-989C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932395 | ||||||
chr9:124932494
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136-1088A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932494 | ||||||
chr9:124932668
|
T | C | 1 | a0003c0004t0006g0065 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136-1262A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932668 | ||||||
chr9:124932881
|
A | G | 1 | a0001c0005t0005g0332 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.136-1475T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932881 | ||||||
chr9:124932894
|
T | C | 245 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(242): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.136-1488A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932894 | ||||||
chr9:124932975
|
T | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1569A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932975 | ||||||
chr9:124932980
|
A | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1574T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932980 | ||||||
chr9:124932982
|
A | T | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1576T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932982 | ||||||
chr9:124932983
|
T | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1577A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932983 | ||||||
chr9:124932984
|
A | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1578T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932984 | ||||||
chr9:124932998
|
A | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1592T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124932998 | ||||||
chr9:124933005
|
T | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1599A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933005 | ||||||
chr9:124933025
|
G | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1619C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933025 | ||||||
chr9:124933026
|
T | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1620A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933026 | ||||||
chr9:124933030
|
A | T | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1624T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933030 | ||||||
chr9:124933041
|
T | G | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1635A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933041 | ||||||
chr9:124933044
|
T | G | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1638A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933044 | ||||||
chr9:124933045
|
T | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1639A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933045 | ||||||
chr9:124933046
|
A | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1640T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933046 | ||||||
chr9:124933047
|
T | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1641A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933047 | ||||||
chr9:124933056
|
G | T | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1650C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933056 | ||||||
chr9:124933058
|
G | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1652C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933058 | ||||||
chr9:124933065
|
A | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1659T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933065 | ||||||
chr9:124933066
|
G | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1660C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933066 | ||||||
chr9:124933067
|
G | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1661C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933067 | ||||||
chr9:124933079
|
G | GCAGTAGA others(3): Show |
1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1674_136-1673i others(12): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933079 | ||||||
chr9:124933081
|
C | T | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1675G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933081 | ||||||
chr9:124933084
|
A | C | 57 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0020others(54): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.136-1678T>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933084 | ||||||
chr9:124933275
|
T | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1869A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933275 | ||||||
chr9:124933276
|
T | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1870A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933276 | ||||||
chr9:124933277
|
G | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1871C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933277 | ||||||
chr9:124933278
|
G | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1872C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933278 | ||||||
chr9:124933281
|
C | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1875G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933281 | ||||||
chr9:124933282
|
T | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1876A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933282 | ||||||
chr9:124933283
|
T | G | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1877A>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933283 | ||||||
chr9:124933285
|
G | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1879C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933285 | ||||||
chr9:124933286
|
C | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1880G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933286 | ||||||
chr9:124933287
|
T | C | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1881A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933287 | ||||||
chr9:124933297
|
G | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1891C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933297 | ||||||
chr9:124933301
|
T | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1895A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933301 | ||||||
chr9:124933316
|
G | A | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-1910C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933316 | ||||||
chr9:124933382
|
G | C | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-1976C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933382 | ||||||
chr9:124933413
|
A | ATTAT | 20 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0124others(17): Show | 23 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.136-2011_136-2008d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933413 | ||||||
chr9:124933422
|
TTATTTAT others(46): Show |
T | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-2069_136-2017d others(55): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933422 | ||||||
chr9:124933697
|
G | A | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-2291C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933697 | ||||||
chr9:124933794
|
C | T | 3 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0121 | 3 | NA18960.hp2 NA18969.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.136-2388G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933794 | ||||||
chr9:124933914
|
C | CTCATGCA others(52): Show |
1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-2509_136-2508i others(61): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933914 | ||||||
chr9:124933920
|
G | C | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-2514C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124933920 | ||||||
chr9:124934015
|
T | A | 3 | a0002c0003t0001g0229a0002c0003t0001g0230a0002c0003t0001g0231 | 3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.136-2609A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934015 | ||||||
chr9:124934019
|
AGTCCTCC others(2306): Show |
A | 3 | a0002c0003t0001g0229a0002c0003t0001g0230a0002c0003t0001g0231 | 3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.135+2245_136-2614d others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934019 | ||||||
chr9:124934112
|
T | C | 1 | a0001c0014t0003g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.136-2706A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934112 | ||||||
chr9:124934231
|
G | A | 12 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-2825C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934231 | ||||||
chr9:124934263
|
G | C | 2 | a0001c0001t0002g0179a0001c0001t0002g0180 | 2 | NA18988.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.136-2857C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934263 | ||||||
chr9:124934291
|
G | A | 4 | a0004c0007t0007g0051a0004c0007t0007g0052a0004c0007t0007g0053others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-2885C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934291 | ||||||
chr9:124934440
|
G | C | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-3034C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934440 | ||||||
chr9:124934520
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136-3114C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124934520 | ||||||
chr9:124935175
|
T | A | 2 | a0002c0002t0001g0319a0002c0002t0001g0326 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.135+3402A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935175 | ||||||
chr9:124935288
|
G | A | 49 | a0001c0001t0002g0205a0001c0001t0016g0041a0002c0003t0001g0001others(46): Show | 55 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.135+3289C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935288 | ||||||
chr9:124935615
|
G | A | 4 | a0003c0004t0006g0059a0003c0004t0006g0063a0003c0004t0006g0064others(1): Show | 4 | HG02258.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+2962C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935615 | ||||||
chr9:124935763
|
CA | C | 218 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(215): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.135+2813delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935763 | ||||||
chr9:124935763
|
CAA | C | 16 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(13): Show | 20 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+2812_135+2813d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935763 | ||||||
chr9:124935781
|
A | G | 1 | a0003c0004t0006g0248 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.135+2796T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935781 | ||||||
chr9:124935995
|
A | G | 1 | a0002c0002t0001g0251 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.135+2582T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124935995 | ||||||
chr9:124936046
|
T | C | 1 | a0001c0001t0003g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.135+2531A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936046 | ||||||
chr9:124936148
|
C | T | 3 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0044 | 3 | HG00639.hp1 HG01358.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.135+2429G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936148 | ||||||
chr9:124936155
|
G | T | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+2422C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936155 | ||||||
chr9:124936222
|
TATTTCCT others(37): Show |
T | 1 | a0001c0005t0005g0333 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135+2311_135+2354d others(46): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936222 | ||||||
chr9:124936260
|
T | C | 4 | a0004c0007t0007g0051a0004c0007t0007g0052a0004c0007t0007g0053others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+2317A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936260 | ||||||
chr9:124936333
|
T | C | 3 | a0002c0003t0001g0229a0002c0003t0001g0230a0002c0003t0001g0231 | 3 | NA18952.hp2 NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.135+2244A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936333 | ||||||
chr9:124936410
|
A | T | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2167T>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936410 | ||||||
chr9:124936444
|
T | A | 1 | a0001c0001t0004g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.135+2133A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936444 | ||||||
chr9:124936609
|
T | TA | 7 | a0001c0001t0003g0103a0002c0002t0001g0312a0002c0006t0003g0104others(4): Show | 7 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+1967dupT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936609 | ||||||
chr9:124936609
|
TA | T | 6 | a0001c0001t0002g0123a0001c0001t0003g0080a0001c0001t0004g0233others(3): Show | 6 | HG01993.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+1967delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936609 | ||||||
chr9:124936779
|
T | C | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+1798A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936779 | ||||||
chr9:124936834
|
T | C | 1 | a0001c0001t0016g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.135+1743A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124936834 | ||||||
chr9:124937009
|
G | C | 2 | a0002c0003t0012g0113a0002c0003t0012g0114 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.135+1568C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937009 | ||||||
chr9:124937044
|
G | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.135+1533C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937044 | ||||||
chr9:124937092
|
G | A | 1 | a0002c0003t0001g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.135+1485C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937092 | ||||||
chr9:124937127
|
T | TTA | 5 | a0002c0006t0003g0104a0002c0006t0003g0105a0002c0006t0003g0106others(2): Show | 5 | HG01167.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+1448_135+1449d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937127 | ||||||
chr9:124937143
|
C | T | 160 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(157): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.135+1434G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937143 | ||||||
chr9:124937189
|
C | T | 143 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(140): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.135+1388G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937189 | ||||||
chr9:124937219
|
C | T | 1 | a0002c0003t0001g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.135+1358G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937219 | ||||||
chr9:124937233
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.135+1344G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937233 | ||||||
chr9:124937312
|
C | T | 1 | a0002c0002t0001g0313 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.135+1265G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937312 | ||||||
chr9:124937330
|
T | A | 3 | a0003c0004t0006g0059a0003c0004t0006g0064a0003c0004t0006g0065 | 3 | HG02258.hp1 HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.135+1247A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937330 | ||||||
chr9:124937331
|
A | G | 5 | a0002c0002t0001g0031a0002c0002t0001g0267a0002c0002t0001g0316others(2): Show | 6 | HG02622.hp1 HG02886.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+1246T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937331 | ||||||
chr9:124937368
|
G | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+1209C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937368 | ||||||
chr9:124937421
|
C | T | 4 | a0004c0007t0007g0051a0004c0007t0007g0052a0004c0007t0007g0053others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+1156G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937421 | ||||||
chr9:124937435
|
A | G | 143 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(140): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.135+1142T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937435 | ||||||
chr9:124937488
|
G | A | 3 | a0002c0002t0001g0029a0002c0002t0001g0313a0002c0002t0001g0314 | 4 | HG00140.hp2 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+1089C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937488 | ||||||
chr9:124937521
|
C | T | 4 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0121others(1): Show | 4 | HG00423.hp1 NA18960.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+1056G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937521 | ||||||
chr9:124937552
|
A | G | 1 | a0005c0016t0001g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+1025T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937552 | ||||||
chr9:124937569
|
T | A | 1 | a0012c0017t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.135+1008A>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937569 | ||||||
chr9:124937592
|
C | T | 1 | a0003c0004t0006g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.135+985G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937592 | ||||||
chr9:124937630
|
CA | C | 186 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(183): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.135+946delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937630 | ||||||
chr9:124937682
|
G | A | 1 | a0002c0002t0001g0263 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.135+895C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937682 | ||||||
chr9:124937759
|
T | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0120a0001c0001t0002g0182 | 4 | HG01081.hp2 HG01346.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+818A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937759 | ||||||
chr9:124937904
|
A | G | 186 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(183): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.135+673T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937904 | ||||||
chr9:124937956
|
A | G | 1 | a0003c0004t0009g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135+621T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937956 | ||||||
chr9:124937976
|
G | A | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG02132.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.135+601C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124937976 | ||||||
chr9:124938037
|
C | G | 1 | a0002c0002t0001g0264 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.135+540G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938037 | ||||||
chr9:124938069
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.135+508G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938069 | ||||||
chr9:124938082
|
C | CAA | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+493_135+494dup others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938082 | ||||||
chr9:124938082
|
CA | C | 56 | a0001c0001t0002g0067a0001c0001t0002g0205a0001c0001t0004g0232others(53): Show | 62 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.135+494delT | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938082 | ||||||
chr9:124938098
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.135+479T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938098 | ||||||
chr9:124938271
|
C | T | 1 | a0002c0002t0001g0250 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.135+306G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938271 | ||||||
chr9:124938382
|
G | C | 100 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(97): Show | 108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.135+195C>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938382 | ||||||
chr9:124938388
|
AAT | A | 238 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(235): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.135+187_135+188del others(2): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938388 | ||||||
chr9:124938399
|
C | A | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+178G>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938399 | ||||||
chr9:124938437
|
C | G | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.135+140G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938437 | ||||||
chr9:124938497
|
G | T | 1 | a0008c0011t0003g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+80C>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 3/22 | chr9 | 124938497 | ||||||
chr9:124939028
|
C | T | 1 | a0002c0002t0001g0262 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-155-162G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939028 | ||||||
chr9:124939527
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-156+579G>A | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939527 | ||||||
chr9:124939538
|
T | TTTTC | 16 | a0002c0002t0001g0004a0002c0002t0001g0031a0002c0002t0001g0032others(13): Show | 21 | HG00438.hp2 HG02080.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.-156+564_-156+567d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939538 | ||||||
chr9:124939546
|
CTTTCTTT | C | 9 | a0003c0004t0006g0059a0003c0004t0006g0062a0003c0004t0006g0063others(6): Show | 9 | HG01069.hp2 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-156+553_-156+559d others(9): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939546 | ||||||
chr9:124939550
|
C | CT | 15 | a0001c0001t0008g0035a0002c0002t0001g0023a0002c0002t0001g0250others(12): Show | 16 | HG00558.hp2 HG00738.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-156+555dupA | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | ||||||
chr9:124939550
|
CTTT | C | 32 | a0001c0001t0002g0006a0001c0001t0002g0066a0001c0001t0002g0067others(29): Show | 37 | HG00597.hp2 HG00621.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.-156+553_-156+555d others(5): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | ||||||
chr9:124939550
|
CTTTT | C | 77 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(74): Show | 84 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-156+552_-156+555d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | ||||||
chr9:124939550
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0001g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-156+545_-156+555d others(13): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | ||||||
chr9:124939550
|
CTTTTTTT others(5): Show |
C | 48 | a0001c0001t0002g0205a0002c0003t0001g0001a0002c0003t0001g0017others(45): Show | 54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-156+544_-156+555d others(14): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939550 | ||||||
chr9:124939552
|
T | TTC | 18 | a0001c0001t0002g0057a0001c0001t0003g0042a0001c0001t0003g0043others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-156+553_-156+554i others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939552 | ||||||
chr9:124939553
|
T | TC | 43 | a0001c0001t0002g0249a0001c0001t0003g0007a0001c0001t0003g0008others(40): Show | 50 | HG00099.hp1 HG00738.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.-156+552_-156+553i others(3): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939553 | ||||||
chr9:124939554
|
T | C | 3 | a0001c0001t0002g0112a0001c0001t0003g0111a0005c0016t0001g0110 | 3 | HG01109.hp2 HG01169.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-156+552A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939554 | ||||||
chr9:124939556
|
T | C | 2 | a0002c0003t0012g0113a0002c0003t0012g0114 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-156+550A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939556 | ||||||
chr9:124939557
|
T | C | 20 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0117others(17): Show | 24 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.-156+549A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939557 | ||||||
chr9:124939558
|
T | C | 76 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(73): Show | 83 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-156+548A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939558 | ||||||
chr9:124939559
|
T | C | 2 | a0001c0001t0002g0185a0001c0001t0002g0186 | 2 | HG02976.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-156+547A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939559 | ||||||
chr9:124939560
|
T | C | 1 | a0002c0002t0001g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-156+546A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939560 | ||||||
chr9:124939561
|
T | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.-156+545A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939561 | ||||||
chr9:124939563
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-156+543A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939563 | ||||||
chr9:124939565
|
T | C | 1 | a0002c0003t0001g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-156+541A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939565 | ||||||
chr9:124939566
|
T | C | 48 | a0001c0001t0002g0205a0002c0003t0001g0001a0002c0003t0001g0017others(45): Show | 54 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-156+540A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939566 | ||||||
chr9:124939593
|
G | A | 1 | a0001c0001t0002g0020 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-156+513C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939593 | ||||||
chr9:124939596
|
CTT | C | 15 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0022others(12): Show | 19 | HG00621.hp1 HG01123.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.-156+508_-156+509d others(4): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939596 | ||||||
chr9:124939676
|
C | G | 1 | a0001c0001t0010g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-156+430G>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939676 | ||||||
chr9:124939953
|
T | C | 1 | a0002c0002t0001g0329 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-156+153A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 2/22 | chr9 | 124939953 | ||||||
chr9:124940241
|
G | A | 1 | a0003c0004t0006g0248 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-205-86C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940241 | ||||||
chr9:124940490
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-205-335A>G | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940490 | ||||||
chr9:124940681
|
CAAAG | C | 5 | a0001c0005t0005g0005a0001c0005t0005g0033a0001c0005t0005g0332others(2): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-206+286_-206+289d others(6): Show |
GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940681 | ||||||
chr9:124940722
|
A | G | 240 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0012others(237): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-206+249T>C | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940722 | ||||||
chr9:124940880
|
G | A | 1 | a0002c0002t0001g0330 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-206+91C>T | GOLGA1 | ENSG00000136935.14 | transcript | ENST00000373555.9 | protein_coding | 1/22 | chr9 | 124940880 |