geneid | 55750 |
---|---|
ensemblid | ENSG00000006530.18 |
hgncid | 21869 |
symbol | AGK |
name | acylglycerol kinase |
refseq_nuc | NM_018238.4 |
refseq_prot | NP_060708.1 |
ensembl_nuc | ENST00000649286.2 |
ensembl_prot | ENSP00000497280.1 |
mane_status | MANE Select |
chr | chr7 |
start | 141551410 |
end | 141655244 |
strand | + |
ver | v1.2 |
region | chr7:141551410-141655244 |
region5000 | chr7:141546410-141660244 |
regionname0 | AGK_chr7_141551410_141655244 |
regionname5000 | AGK_chr7_141546410_141660244 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 422 | 268 | 68 | 43 | 115 | 8 | 32 | 83 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0002 | 0/0 | 422 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0003 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0004 | 0/0 | 422 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0005 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1269 | 268 | 68 | 43 | 115 | 8 | 32 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
c0002 | 0/0 | 1269 | 3 | 2 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
c0003 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
c0004 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
c0005 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2360 | 216 | 43 | 39 | 102 | 7 | 23 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0002 | 0/0 | 2360 | 24 | 6 | 2 | 10 | 0 | 6 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0003 | 0/0 | 2364 | 8 | 7 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0004 | 0/0 | 2360 | 6 | 6 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0005 | 0/0 | 2360 | 3 | 1 | 0 | 2 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0006 | 0/0 | 2364 | 3 | 3 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0007 | 0/0 | 2360 | 2 | 0 | 1 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0008 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0009 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0010 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0011 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0012 | 0/0 | 2360 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0013 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0014 | 0/0 | 2360 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0015 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0016 | 0/0 | 2360 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
t0017 | 0/0 | 2360 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1269 | 268 | 68 | 43 | 115 | 8 | 32 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0002c0002 | 0/0 | 1269 | 3 | 2 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0003c0003 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0004c0004 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0005c0005 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3628 | 215 | 42 | 39 | 102 | 7 | 23 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0002 | 0/0 | 3628 | 23 | 6 | 2 | 9 | 0 | 6 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0003 | 0/0 | 3632 | 5 | 5 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0004 | 0/0 | 3628 | 6 | 6 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0005 | 0/0 | 3628 | 3 | 1 | 0 | 2 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0006 | 0/0 | 3632 | 3 | 3 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0007 | 0/0 | 3628 | 2 | 0 | 1 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0008 | 0/0 | 3628 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0009 | 0/0 | 3628 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0011 | 0/0 | 3628 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0012 | 0/0 | 3628 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0013 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0014 | 0/0 | 3628 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0015 | 0/0 | 3628 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0016 | 0/0 | 3628 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0001c0001t0017 | 0/0 | 3628 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0002c0002t0003 | 0/0 | 3632 | 3 | 2 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0003c0003t0010 | 0/0 | 3632 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0004c0004t0002 | 0/0 | 3628 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
a0005c0005t0001 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | copy fasta | chr7 | 141546410 | 141660244 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0012g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0013g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0014g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0015g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0016g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0001c0001t0017g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0002c0002t0003g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0002c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0003c0003t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0004c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
a0005c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0015 | EUR | GBR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0054 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01261 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01361 | hp1 | a0001 | c0001 | t0012 | g0041 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0224 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CDX | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02615 | hp1 | a0001 | c0001 | t0013 | g0136 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0120 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02683 | hp1 | a0001 | c0001 | t0016 | g0170 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0119 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0270 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0034 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03041 | hp1 | a0005 | c0005 | t0001 | g0021 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0004 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03942 | hp1 | a0001 | c0001 | t0017 | g0244 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18906 | hp2 | a0003 | c0003 | t0010 | g0227 | AFR | YRI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18951 | hp2 | a0001 | c0001 | t0011 | g0186 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19078 | hp1 | a0004 | c0004 | t0002 | g0245 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ASW | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ASW | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20905 | hp2 | a0001 | c0001 | t0014 | g0006 | SAS | GIH | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0053 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | USA | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0159 | REF | REF | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:141555483
|
A | G | 1 | a0002 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.17A>G | p.Lys6Arg | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/16 | 56/3628 | 17/1269 | 6/422 | chr7 | 141555483 | ||
chr7:141596602
|
A | G | 1 | a0005 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.182A>G | p.Lys61Arg | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/16 | 221/3628 | 182/1269 | 61/422 | chr7 | 141596602 | ||
chr7:141611252
|
A | G | 1 | a0004 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.355A>G | p.Ile119Val | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/16 | 394/3628 | 355/1269 | 119/422 | chr7 | 141611252 | ||
chr7:141614171
|
C | G | 1 | a0003 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.416C>G | p.Thr139Arg | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/16 | 455/3628 | 416/1269 | 139/422 | chr7 | 141614171 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:141653065
|
C | T | 1 | a0001c0001t0004 | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*141C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 141 | chr7 | 141653065 | |||||
chr7:141653068
|
C | A | 1 | a0003c0003t0010 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 144 | chr7 | 141653068 | |||||
chr7:141653108
|
C | T | 1 | a0001c0001t0009 | 2 | HG02622.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 184 | chr7 | 141653108 | |||||
chr7:141653239
|
C | T | 1 | a0001c0001t0017 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*315C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 315 | chr7 | 141653239 | |||||
chr7:141653244
|
G | A | 3 | a0001c0001t0003a0001c0001t0005a0002c0002t0003 | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*320G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 320 | chr7 | 141653244 | |||||
chr7:141653383
|
T | A | 1 | a0001c0001t0011 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 459 | chr7 | 141653383 | |||||
chr7:141653385
|
C | CTGTT | 4 | a0001c0001t0003a0001c0001t0006a0002c0002t0003others(1): Show | 12 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*463_*466dupGTTT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 467 | INFO_REALIGN_3_PRIME | chr7 | 141653385 | ||||
chr7:141653628
|
A | G | 1 | a0001c0001t0016 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*704A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 704 | chr7 | 141653628 | |||||
chr7:141654099
|
C | T | 4 | a0001c0001t0002a0001c0001t0015a0001c0001t0017others(1): Show | 26 | HG00408.hp1 HG00597.hp2 HG01168.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1175C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1175 | chr7 | 141654099 | |||||
chr7:141654134
|
A | T | 2 | a0001c0001t0006a0003c0003t0010 | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1210A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1210 | chr7 | 141654134 | |||||
chr7:141654391
|
T | C | 1 | a0001c0001t0015 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1467T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1467 | chr7 | 141654391 | |||||
chr7:141654673
|
G | A | 1 | a0001c0001t0007 | 2 | HG00140.hp2 HG01123.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1749 | chr7 | 141654673 | |||||
chr7:141654695
|
G | A | 1 | a0001c0001t0012 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1771G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1771 | chr7 | 141654695 | |||||
chr7:141654934
|
A | G | 1 | a0001c0001t0008 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2010A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 2010 | chr7 | 141654934 | |||||
chr7:141654942
|
C | T | 1 | a0001c0001t0014 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 2018 | chr7 | 141654942 | |||||
chr7:141655072
|
C | A | 1 | a0001c0001t0006 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2148C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 2148 | chr7 | 141655072 | |||||
chr7:141655089
|
G | A | 1 | a0001c0001t0013 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 2165 | chr7 | 141655089 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:141551465
|
C | G | 49 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(46): Show | 51 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.-15+31C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551465 | ||||||
chr7:141551493
|
G | T | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-15+59G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551493 | ||||||
chr7:141551642
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0223 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+208C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551642 | ||||||
chr7:141551768
|
C | T | 49 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(46): Show | 51 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.-15+334C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551768 | ||||||
chr7:141551808
|
GGGTT | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG00642.hp2 HG01168.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+383_-15+386del others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 141551808 | |||||
chr7:141551910
|
T | G | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-15+476T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551910 | ||||||
chr7:141551973
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15+539C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551973 | ||||||
chr7:141552086
|
C | G | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+652C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552086 | ||||||
chr7:141552380
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-15+946A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552380 | ||||||
chr7:141552479
|
T | G | 4 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1045T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552479 | ||||||
chr7:141552605
|
A | G | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-15+1171A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552605 | ||||||
chr7:141552607
|
G | A | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-15+1173G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552607 | ||||||
chr7:141552623
|
T | G | 1 | a0001c0001t0001g0011 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-15+1189T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552623 | ||||||
chr7:141552626
|
C | T | 4 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1192C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552626 | ||||||
chr7:141552627
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0002g0229 | 2 | HG01952.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-15+1193G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552627 | ||||||
chr7:141552682
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15+1248G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552682 | ||||||
chr7:141552753
|
T | C | 150 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(147): Show | 152 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-15+1319T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552753 | ||||||
chr7:141552762
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+1328G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552762 | ||||||
chr7:141553616
|
G | T | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14-1837G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141553616 | ||||||
chr7:141553729
|
C | T | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-14-1724C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141553729 | ||||||
chr7:141553827
|
G | A | 23 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(20): Show | 23 | HG00408.hp1 HG01952.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-1626G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141553827 | ||||||
chr7:141553915
|
C | T | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-14-1538C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141553915 | ||||||
chr7:141554051
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14-1402G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554051 | ||||||
chr7:141554077
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-14-1376C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554077 | ||||||
chr7:141554338
|
T | TA | 17 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(14): Show | 18 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-14-1096dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 141554338 | |||||
chr7:141554481
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-14-972G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554481 | ||||||
chr7:141554495
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-958C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554495 | ||||||
chr7:141554600
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-853G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554600 | ||||||
chr7:141554691
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-14-762T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554691 | ||||||
chr7:141554694
|
C | T | 47 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(44): Show | 49 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.-14-759C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554694 | ||||||
chr7:141554923
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-14-530A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554923 | ||||||
chr7:141555050
|
T | C | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-403T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141555050 | ||||||
chr7:141555096
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-14-357A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141555096 | ||||||
chr7:141555178
|
G | C | 1 | a0001c0001t0002g0230 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-14-275G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141555178 | ||||||
chr7:141555184
|
A | G | 26 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(23): Show | 26 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.-14-269A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141555184 | ||||||
chr7:141555572
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | splice_region_variant&intron_variant | LOW | c.101+5C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141555572 | ||||||
chr7:141555638
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+71A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141555638 | ||||||
chr7:141556095
|
T | C | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+528T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556095 | ||||||
chr7:141556289
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.101+722G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556289 | ||||||
chr7:141556489
|
C | T | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+922C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556489 | ||||||
chr7:141556497
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.101+930G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556497 | ||||||
chr7:141556540
|
C | CA | 14 | a0001c0001t0001g0014a0001c0001t0001g0104a0001c0001t0001g0111others(11): Show | 14 | HG00140.hp2 HG01168.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.101+990dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141556540 | |||||
chr7:141556583
|
C | T | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101+1016C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556583 | ||||||
chr7:141556748
|
T | G | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.101+1181T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556748 | ||||||
chr7:141557066
|
C | G | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.101+1499C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557066 | ||||||
chr7:141557130
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101+1563T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557130 | ||||||
chr7:141557196
|
A | T | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101+1629A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557196 | ||||||
chr7:141557247
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101+1680T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557247 | ||||||
chr7:141557480
|
G | A | 26 | a0001c0001t0001g0016a0001c0001t0002g0219a0001c0001t0002g0229others(23): Show | 26 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.101+1913G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557480 | ||||||
chr7:141557964
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.101+2397A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557964 | ||||||
chr7:141558007
|
C | T | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.101+2440C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558007 | ||||||
chr7:141558180
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02083.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.101+2613C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558180 | ||||||
chr7:141558250
|
G | A | 9 | a0001c0001t0001g0116a0001c0001t0001g0228a0001c0001t0003g0265others(6): Show | 10 | HG01261.hp1 HG02559.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+2683G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558250 | ||||||
chr7:141558347
|
GT | G | 41 | a0001c0001t0001g0104a0001c0001t0001g0228a0001c0001t0002g0219others(38): Show | 43 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.101+2794delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141558347 | |||||
chr7:141558348
|
T | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0230 | 3 | HG01081.hp2 NA19064.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.101+2781T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558348 | ||||||
chr7:141558349
|
T | G | 41 | a0001c0001t0001g0104a0001c0001t0001g0228a0001c0001t0002g0219others(38): Show | 43 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.101+2782T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558349 | ||||||
chr7:141558411
|
C | A | 2 | a0001c0001t0009g0119a0001c0001t0009g0120 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.101+2844C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558411 | ||||||
chr7:141558457
|
G | A | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.101+2890G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558457 | ||||||
chr7:141558500
|
G | A | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+2933G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558500 | ||||||
chr7:141558579
|
T | C | 42 | a0001c0001t0001g0104a0001c0001t0001g0228a0001c0001t0002g0219others(39): Show | 44 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.101+3012T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558579 | ||||||
chr7:141558590
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.101+3023A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558590 | ||||||
chr7:141558652
|
G | A | 4 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0232others(1): Show | 4 | HG01952.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+3085G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558652 | ||||||
chr7:141558720
|
G | T | 1 | a0001c0001t0001g0215 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.101+3153G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558720 | ||||||
chr7:141558760
|
T | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+3193T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558760 | ||||||
chr7:141558805
|
T | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0234 | 2 | NA18997.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.101+3238T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558805 | ||||||
chr7:141559004
|
A | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+3437A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559004 | ||||||
chr7:141559093
|
C | T | 3 | a0001c0001t0002g0251a0001c0001t0005g0261a0001c0001t0005g0262 | 3 | NA18949.hp2 NA18959.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.101+3526C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559093 | ||||||
chr7:141559168
|
T | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+3601T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559168 | ||||||
chr7:141559238
|
T | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+3671T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559238 | ||||||
chr7:141559387
|
C | T | 7 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG00544.hp2 HG03209.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.101+3820C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559387 | ||||||
chr7:141559665
|
T | C | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+4098T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559665 | ||||||
chr7:141559694
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.101+4127C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559694 | ||||||
chr7:141559752
|
CT | C | 23 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(20): Show | 23 | HG00408.hp1 HG01952.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.101+4188delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141559752 | |||||
chr7:141559810
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.101+4243T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559810 | ||||||
chr7:141559959
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.101+4392G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559959 | ||||||
chr7:141559969
|
C | CT | 67 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0098others(64): Show | 69 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.101+4412dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141559969 | |||||
chr7:141560271
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.101+4704C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560271 | ||||||
chr7:141560272
|
G | T | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.101+4705G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560272 | ||||||
chr7:141560284
|
G | C | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.101+4717G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560284 | ||||||
chr7:141560403
|
TTTC | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+4848_101+4850d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141560403 | |||||
chr7:141560560
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.101+4993G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560560 | ||||||
chr7:141560762
|
A | G | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+5195A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560762 | ||||||
chr7:141560795
|
C | CT | 108 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 108 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.101+5247dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141560795 | |||||
chr7:141560799
|
T | C | 9 | a0001c0001t0001g0228a0001c0001t0003g0265a0001c0001t0003g0266others(6): Show | 10 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+5232T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560799 | ||||||
chr7:141560800
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.101+5233T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560800 | ||||||
chr7:141560852
|
A | G | 36 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(33): Show | 37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.101+5285A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560852 | ||||||
chr7:141560859
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.101+5292C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560859 | ||||||
chr7:141560880
|
T | TCCGC | 9 | a0001c0001t0001g0228a0001c0001t0003g0265a0001c0001t0003g0266others(6): Show | 10 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+5315_101+5318d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141560880 | |||||
chr7:141560994
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.101+5427C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560994 | ||||||
chr7:141560995
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.101+5428G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560995 | ||||||
chr7:141561029
|
G | A | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.101+5462G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561029 | ||||||
chr7:141561088
|
C | T | 6 | a0001c0001t0001g0109a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG01070.hp1 HG01099.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+5521C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561088 | ||||||
chr7:141561142
|
T | C | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101+5575T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561142 | ||||||
chr7:141561354
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.101+5787C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561354 | ||||||
chr7:141561487
|
TA | T | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+5921delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561487 | ||||||
chr7:141561496
|
T | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01070.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.101+5929T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561496 | ||||||
chr7:141561614
|
A | AT | 6 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(3): Show | 7 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+6057dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141561614 | |||||
chr7:141561623
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+6056T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561623 | ||||||
chr7:141561669
|
G | T | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+6102G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561669 | ||||||
chr7:141561687
|
C | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+6120C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561687 | ||||||
chr7:141562150
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.101+6583C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562150 | ||||||
chr7:141562274
|
T | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(266): Show | 273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.101+6707T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562274 | ||||||
chr7:141562357
|
C | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+6790C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562357 | ||||||
chr7:141562542
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.101+6975A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562542 | ||||||
chr7:141562585
|
G | T | 1 | a0001c0001t0004g0256 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101+7018G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562585 | ||||||
chr7:141562765
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.101+7198G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562765 | ||||||
chr7:141563026
|
G | A | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+7459G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563026 | ||||||
chr7:141563106
|
G | A | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+7539G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563106 | ||||||
chr7:141563107
|
T | G | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+7540T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563107 | ||||||
chr7:141563226
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.101+7659G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563226 | ||||||
chr7:141563366
|
T | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+7799T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563366 | ||||||
chr7:141563666
|
G | T | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+8099G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563666 | ||||||
chr7:141563837
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.101+8270C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563837 | ||||||
chr7:141563963
|
G | C | 1 | a0001c0001t0002g0263 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.101+8396G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563963 | ||||||
chr7:141563989
|
C | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+8422C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563989 | ||||||
chr7:141563992
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0124 | 2 | HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.101+8425G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563992 | ||||||
chr7:141564016
|
A | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+8449A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564016 | ||||||
chr7:141564200
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+8633T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564200 | ||||||
chr7:141564251
|
T | C | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+8684T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564251 | ||||||
chr7:141564469
|
AACTC | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0001t0001g0108others(18): Show | 21 | HG00642.hp1 HG01255.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.101+8910_101+8913d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141564469 | |||||
chr7:141564531
|
A | G | 4 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0232others(1): Show | 4 | HG01952.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+8964A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564531 | ||||||
chr7:141564551
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101+8984C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564551 | ||||||
chr7:141564579
|
G | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+9012G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564579 | ||||||
chr7:141564647
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101+9080C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564647 | ||||||
chr7:141564800
|
A | G | 149 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(146): Show | 151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.101+9233A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564800 | ||||||
chr7:141564844
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.101+9277C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564844 | ||||||
chr7:141564898
|
T | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+9331T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564898 | ||||||
chr7:141564956
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.101+9389A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564956 | ||||||
chr7:141565131
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+9564C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565131 | ||||||
chr7:141565244
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+9677C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565244 | ||||||
chr7:141565421
|
C | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+9854C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565421 | ||||||
chr7:141565448
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.101+9881C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565448 | ||||||
chr7:141565498
|
A | C | 1 | a0001c0001t0001g0011 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.101+9931A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565498 | ||||||
chr7:141565585
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.101+10018G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565585 | ||||||
chr7:141565637
|
C | CA | 7 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0097others(4): Show | 7 | HG01243.hp1 HG02683.hp2 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.101+10085dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141565637 | |||||
chr7:141565706
|
C | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG00544.hp1 HG02040.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+10139C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565706 | ||||||
chr7:141565800
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG02602.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.101+10233A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565800 | ||||||
chr7:141565891
|
G | T | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101+10324G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565891 | ||||||
chr7:141566025
|
G | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.101+10458G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566025 | ||||||
chr7:141566086
|
T | C | 10 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(7): Show | 11 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+10519T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566086 | ||||||
chr7:141566104
|
C | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+10537C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566104 | ||||||
chr7:141566141
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.101+10574A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566141 | ||||||
chr7:141566208
|
A | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+10641A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566208 | ||||||
chr7:141566470
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.101+10903G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566470 | ||||||
chr7:141566587
|
G | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+11020G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566587 | ||||||
chr7:141566713
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG01496.hp2 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.101+11146G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566713 | ||||||
chr7:141566714
|
C | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+11147C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566714 | ||||||
chr7:141567021
|
A | G | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+11454A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567021 | ||||||
chr7:141567167
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0223 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.101+11600C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567167 | ||||||
chr7:141567194
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0162 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.101+11627C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567194 | ||||||
chr7:141567433
|
A | T | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.101+11866A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567433 | ||||||
chr7:141567469
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101+11902T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567469 | ||||||
chr7:141567543
|
A | G | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 9 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+11976A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567543 | ||||||
chr7:141567619
|
T | C | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+12052T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567619 | ||||||
chr7:141567852
|
T | C | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+12285T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567852 | ||||||
chr7:141568057
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.101+12490C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568057 | ||||||
chr7:141568218
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18977.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.101+12651A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568218 | ||||||
chr7:141568291
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.101+12724G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568291 | ||||||
chr7:141568574
|
C | CT | 15 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(12): Show | 16 | HG01884.hp1 HG01891.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.101+13022dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141568574 | |||||
chr7:141568625
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.101+13058G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568625 | ||||||
chr7:141568657
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.101+13090C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568657 | ||||||
chr7:141568774
|
C | A | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101+13207C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568774 | ||||||
chr7:141568842
|
C | T | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101+13275C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568842 | ||||||
chr7:141568971
|
T | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0145a0001c0001t0001g0156others(1): Show | 4 | HG02602.hp1 HG03688.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+13404T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568971 | ||||||
chr7:141569047
|
C | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+13480C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569047 | ||||||
chr7:141569217
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.101+13650C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569217 | ||||||
chr7:141569232
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.101+13665C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569232 | ||||||
chr7:141569306
|
C | T | 9 | a0001c0001t0001g0110a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.101+13739C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569306 | ||||||
chr7:141569464
|
G | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+13897G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569464 | ||||||
chr7:141569592
|
C | T | 46 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0022others(43): Show | 46 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.101+14025C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569592 | ||||||
chr7:141569634
|
A | G | 9 | a0001c0001t0001g0228a0001c0001t0003g0265a0001c0001t0003g0266others(6): Show | 10 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+14067A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569634 | ||||||
chr7:141569693
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101+14126C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569693 | ||||||
chr7:141569704
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101+14137G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569704 | ||||||
chr7:141569782
|
G | A | 1 | a0001c0001t0016g0170 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.101+14215G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569782 | ||||||
chr7:141569827
|
A | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG01081.hp1 HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.101+14260A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569827 | ||||||
chr7:141569829
|
C | T | 10 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(7): Show | 11 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+14262C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569829 | ||||||
chr7:141569923
|
G | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+14356G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569923 | ||||||
chr7:141570061
|
G | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0202others(1): Show | 4 | NA18948.hp1 NA19000.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+14494G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570061 | ||||||
chr7:141570100
|
A | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+14533A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570100 | ||||||
chr7:141570123
|
C | T | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+14556C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570123 | ||||||
chr7:141570295
|
CAGA | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0143 | 3 | HG01081.hp2 HG03927.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.101+14730_101+1473 others(7): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141570295 | |||||
chr7:141570436
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.101+14869A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570436 | ||||||
chr7:141570462
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101+14895C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570462 | ||||||
chr7:141570646
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101+15079A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570646 | ||||||
chr7:141571060
|
G | C | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.101+15493G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141571060 | ||||||
chr7:141571266
|
T | C | 9 | a0001c0001t0001g0228a0001c0001t0003g0265a0001c0001t0003g0266others(6): Show | 10 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+15699T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141571266 | ||||||
chr7:141571823
|
G | C | 1 | a0001c0001t0002g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.101+16256G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141571823 | ||||||
chr7:141571841
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101+16274A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141571841 | ||||||
chr7:141572242
|
A | C | 1 | a0001c0001t0007g0015 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.101+16675A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572242 | ||||||
chr7:141572499
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.101+16932T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572499 | ||||||
chr7:141572731
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0223 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.101+17164G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572731 | ||||||
chr7:141572803
|
TG | T | 26 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(23): Show | 26 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.101+17245delG | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141572803 | |||||
chr7:141572806
|
G | C | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+17239G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572806 | ||||||
chr7:141572807
|
G | C | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+17240G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572807 | ||||||
chr7:141572809
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.101+17242G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572809 | ||||||
chr7:141572828
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.101+17261C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572828 | ||||||
chr7:141572916
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(38): Show | 42 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.101+17349G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572916 | ||||||
chr7:141573016
|
G | T | 36 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(33): Show | 37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.101+17449G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573016 | ||||||
chr7:141573226
|
T | A | 1 | a0001c0001t0001g0061 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.101+17659T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573226 | ||||||
chr7:141573360
|
A | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG02602.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.101+17793A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573360 | ||||||
chr7:141573703
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+18136C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573703 | ||||||
chr7:141573796
|
G | A | 35 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(32): Show | 36 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.101+18229G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573796 | ||||||
chr7:141573827
|
T | C | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+18260T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573827 | ||||||
chr7:141573829
|
C | T | 10 | a0001c0001t0001g0228a0001c0001t0003g0265a0001c0001t0003g0266others(7): Show | 11 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+18262C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573829 | ||||||
chr7:141574443
|
G | A | 1 | a0002c0002t0003g0004 | 2 | HG01261.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-18703G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574443 | ||||||
chr7:141574578
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.102-18568G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574578 | ||||||
chr7:141574591
|
G | C | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.102-18555G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574591 | ||||||
chr7:141574637
|
A | T | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.102-18509A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574637 | ||||||
chr7:141574754
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.102-18392A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574754 | ||||||
chr7:141574758
|
G | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-18388G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574758 | ||||||
chr7:141574860
|
GGGAGCGA others(9): Show |
G | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.102-18283_102-1826 others(20): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141574860 | |||||
chr7:141574944
|
G | T | 1 | a0004c0004t0002g0245 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.102-18202G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574944 | ||||||
chr7:141575009
|
A | G | 1 | a0001c0001t0017g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.102-18137A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575009 | ||||||
chr7:141575119
|
G | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-18027G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575119 | ||||||
chr7:141575457
|
T | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | NA18991.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.102-17689T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575457 | ||||||
chr7:141575654
|
C | CT | 62 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0026others(59): Show | 62 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.102-17463dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | |||||
chr7:141575654
|
C | CTT | 9 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0028others(6): Show | 9 | HG00558.hp2 HG00642.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.102-17464_102-1746 others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | |||||
chr7:141575654
|
CT | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0146a0001c0001t0001g0220others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-17463delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | |||||
chr7:141575654
|
CTTT | C | 6 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(3): Show | 6 | HG02015.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-17465_102-1746 others(7): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | |||||
chr7:141575654
|
CTTTT | C | 18 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0002g0234others(15): Show | 18 | HG00408.hp1 HG02155.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.102-17466_102-1746 others(8): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | |||||
chr7:141575654
|
CTTTTT | C | 12 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0231others(9): Show | 13 | HG01168.hp2 HG01884.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-17467_102-1746 others(9): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | |||||
chr7:141575654
|
CTTTTTT | C | 5 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0269others(2): Show | 6 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-17468_102-1746 others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | |||||
chr7:141575654
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0173 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.102-17475_102-1746 others(17): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | |||||
chr7:141575683
|
T | G | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-17463T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575683 | ||||||
chr7:141575687
|
C | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-17459C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575687 | ||||||
chr7:141575837
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.102-17309C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575837 | ||||||
chr7:141576246
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.102-16900A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576246 | ||||||
chr7:141576263
|
A | G | 36 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(33): Show | 37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.102-16883A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576263 | ||||||
chr7:141576334
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.102-16812C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576334 | ||||||
chr7:141576355
|
CTTG | C | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.102-16786_102-1678 others(7): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141576355 | |||||
chr7:141576404
|
A | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-16742A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576404 | ||||||
chr7:141576427
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.102-16719A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576427 | ||||||
chr7:141576485
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102-16661A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576485 | ||||||
chr7:141576632
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.102-16514C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576632 | ||||||
chr7:141576633
|
G | A | 7 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(4): Show | 7 | HG01891.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-16513G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576633 | ||||||
chr7:141576651
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.102-16495A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576651 | ||||||
chr7:141576765
|
C | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-16381C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576765 | ||||||
chr7:141576847
|
C | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-16299C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576847 | ||||||
chr7:141577035
|
G | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.102-16111G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577035 | ||||||
chr7:141577239
|
A | G | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-15907A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577239 | ||||||
chr7:141577418
|
C | T | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-15728C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577418 | ||||||
chr7:141577614
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-15532G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577614 | ||||||
chr7:141577633
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-15513G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577633 | ||||||
chr7:141577742
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-15404C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577742 | ||||||
chr7:141577796
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.102-15350C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577796 | ||||||
chr7:141577818
|
C | CT | 16 | a0001c0001t0001g0011a0001c0001t0001g0104a0001c0001t0001g0123others(13): Show | 16 | HG01168.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-15310dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141577818 | |||||
chr7:141577818
|
C | CTT | 21 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(18): Show | 21 | HG00408.hp1 HG01952.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.102-15311_102-1531 others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141577818 | |||||
chr7:141577818
|
CT | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0088others(9): Show | 13 | HG01256.hp1 HG01884.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.102-15310delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141577818 | |||||
chr7:141577935
|
C | G | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-15211C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577935 | ||||||
chr7:141578085
|
CGTCCATG others(5958): Show |
C | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.102-14991_102-9027 others(3): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141578085 | |||||
chr7:141578143
|
C | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-15003C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578143 | ||||||
chr7:141578156
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-14990G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578156 | ||||||
chr7:141578313
|
G | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-14833G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578313 | ||||||
chr7:141578323
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.102-14823G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578323 | ||||||
chr7:141578396
|
C | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-14750C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578396 | ||||||
chr7:141578401
|
G | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0222 | 2 | HG00408.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.102-14745G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578401 | ||||||
chr7:141578402
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0222 | 2 | HG00408.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.102-14744C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578402 | ||||||
chr7:141578469
|
C | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-14677C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578469 | ||||||
chr7:141578776
|
CGAATAAG others(4): Show |
C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | NA18991.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.102-14366_102-1435 others(15): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141578776 | |||||
chr7:141578847
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102-14299G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578847 | ||||||
chr7:141579017
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-14129A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579017 | ||||||
chr7:141579027
|
A | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0096 | 2 | NA18975.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.102-14119A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579027 | ||||||
chr7:141579152
|
G | C | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-13994G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579152 | ||||||
chr7:141579249
|
G | C | 1 | a0001c0001t0002g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.102-13897G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579249 | ||||||
chr7:141579270
|
C | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-13876C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579270 | ||||||
chr7:141579308
|
G | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-13838G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579308 | ||||||
chr7:141579336
|
A | C | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-13810A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579336 | ||||||
chr7:141579370
|
T | C | 5 | a0001c0001t0003g0265a0001c0001t0003g0269a0001c0001t0005g0260others(2): Show | 6 | HG01261.hp1 HG02258.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-13776T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579370 | ||||||
chr7:141579380
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.102-13766C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579380 | ||||||
chr7:141579456
|
G | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-13690G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579456 | ||||||
chr7:141579527
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.102-13619G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579527 | ||||||
chr7:141579597
|
C | T | 7 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(4): Show | 8 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-13549C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579597 | ||||||
chr7:141579689
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-13457G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579689 | ||||||
chr7:141579779
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.102-13367C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579779 | ||||||
chr7:141579847
|
T | C | 10 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(7): Show | 11 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-13299T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579847 | ||||||
chr7:141579983
|
G | T | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-13163G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579983 | ||||||
chr7:141580005
|
G | A | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-13141G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580005 | ||||||
chr7:141580220
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.102-12926G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580220 | ||||||
chr7:141580273
|
A | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-12873A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580273 | ||||||
chr7:141580278
|
G | C | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.102-12868G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580278 | ||||||
chr7:141580279
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18977.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.102-12867G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580279 | ||||||
chr7:141580385
|
G | A | 4 | a0001c0001t0003g0265a0001c0001t0003g0269a0002c0002t0003g0004others(1): Show | 5 | HG01261.hp1 HG02896.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-12761G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580385 | ||||||
chr7:141580409
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0008g0033others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-12737T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580409 | ||||||
chr7:141580506
|
C | T | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-12640C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580506 | ||||||
chr7:141580625
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.102-12521G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580625 | ||||||
chr7:141580705
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0045 | 2 | HG02027.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.102-12441C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580705 | ||||||
chr7:141580706
|
G | A | 6 | a0001c0001t0003g0265a0001c0001t0003g0269a0001c0001t0005g0261others(3): Show | 7 | HG01261.hp1 HG02896.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-12440G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580706 | ||||||
chr7:141580798
|
G | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.102-12348G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580798 | ||||||
chr7:141580891
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-12255C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580891 | ||||||
chr7:141580915
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0096 | 2 | NA18975.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.102-12231G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580915 | ||||||
chr7:141581010
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0100 | 3 | HG02080.hp2 NA18948.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.102-12136G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581010 | ||||||
chr7:141581081
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102-12065C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581081 | ||||||
chr7:141581246
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-11900G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581246 | ||||||
chr7:141581458
|
G | C | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-11688G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581458 | ||||||
chr7:141581632
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.102-11514A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581632 | ||||||
chr7:141581883
|
T | C | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-11263T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581883 | ||||||
chr7:141581930
|
G | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-11216G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581930 | ||||||
chr7:141582002
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.102-11144C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582002 | ||||||
chr7:141582012
|
G | A | 1 | a0001c0001t0009g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.102-11134G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582012 | ||||||
chr7:141582069
|
C | T | 41 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(38): Show | 43 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.102-11077C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582069 | ||||||
chr7:141582208
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0013g0136 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.102-10938G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582208 | ||||||
chr7:141582295
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102-10851G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582295 | ||||||
chr7:141582340
|
G | A | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-10806G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582340 | ||||||
chr7:141582529
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0162 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.102-10617G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582529 | ||||||
chr7:141582624
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.102-10522T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582624 | ||||||
chr7:141582659
|
G | A | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.102-10487G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582659 | ||||||
chr7:141582768
|
C | G | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-10378C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582768 | ||||||
chr7:141582898
|
G | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-10248G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582898 | ||||||
chr7:141582957
|
A | T | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-10189A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582957 | ||||||
chr7:141582968
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.102-10178A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582968 | ||||||
chr7:141583060
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-10086G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583060 | ||||||
chr7:141583236
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102-9910A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583236 | ||||||
chr7:141583256
|
C | A | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-9890C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583256 | ||||||
chr7:141583353
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.102-9793A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583353 | ||||||
chr7:141583476
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.102-9670C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583476 | ||||||
chr7:141583541
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(200): Show | 206 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.102-9605T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583541 | ||||||
chr7:141583573
|
A | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-9573A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583573 | ||||||
chr7:141583618
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-9528C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583618 | ||||||
chr7:141583711
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.102-9435G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583711 | ||||||
chr7:141583737
|
G | A | 4 | a0001c0001t0003g0265a0001c0001t0003g0269a0002c0002t0003g0004others(1): Show | 5 | HG01261.hp1 HG02896.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-9409G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583737 | ||||||
chr7:141583810
|
C | T | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.102-9336C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583810 | ||||||
chr7:141583951
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.102-9195T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583951 | ||||||
chr7:141584049
|
G | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-9097G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584049 | ||||||
chr7:141584059
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.102-9087G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584059 | ||||||
chr7:141584125
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.102-9021C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584125 | ||||||
chr7:141584131
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.102-9015C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584131 | ||||||
chr7:141584140
|
A | G | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-9006A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584140 | ||||||
chr7:141584166
|
G | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-8980G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584166 | ||||||
chr7:141584256
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG01496.hp2 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.102-8890A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584256 | ||||||
chr7:141584445
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.102-8701C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584445 | ||||||
chr7:141584587
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.102-8559A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584587 | ||||||
chr7:141584593
|
T | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-8553T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584593 | ||||||
chr7:141584865
|
C | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA20752.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.102-8281C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584865 | ||||||
chr7:141584911
|
G | A | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-8235G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584911 | ||||||
chr7:141584930
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.102-8216T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584930 | ||||||
chr7:141585002
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0207 | 2 | NA18957.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.102-8144A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585002 | ||||||
chr7:141585110
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.102-8036G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585110 | ||||||
chr7:141585111
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.102-8035T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585111 | ||||||
chr7:141585174
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-7972G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585174 | ||||||
chr7:141585379
|
C | T | 40 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(37): Show | 41 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.102-7767C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585379 | ||||||
chr7:141585409
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.102-7737G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585409 | ||||||
chr7:141585555
|
G | A | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-7591G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585555 | ||||||
chr7:141585706
|
A | G | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.102-7440A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585706 | ||||||
chr7:141585910
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.102-7236T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585910 | ||||||
chr7:141586034
|
G | A | 2 | a0001c0001t0003g0266a0001c0001t0003g0268 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.102-7112G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586034 | ||||||
chr7:141586098
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02055.hp2 HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.102-7048C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586098 | ||||||
chr7:141586156
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102-6990C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586156 | ||||||
chr7:141586337
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0043 | 2 | HG00735.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.102-6809C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586337 | ||||||
chr7:141586475
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.102-6671A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586475 | ||||||
chr7:141586663
|
A | C | 2 | a0001c0001t0001g0132a0001c0001t0013g0136 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.102-6483A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586663 | ||||||
chr7:141586672
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102-6474A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586672 | ||||||
chr7:141586831
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.102-6315G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586831 | ||||||
chr7:141586956
|
G | A | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.102-6190G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586956 | ||||||
chr7:141587021
|
C | T | 40 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(37): Show | 41 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.102-6125C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587021 | ||||||
chr7:141587040
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.102-6106G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587040 | ||||||
chr7:141587067
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0032others(3): Show | 6 | HG02735.hp2 HG02738.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-6079G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587067 | ||||||
chr7:141587085
|
T | C | 152 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(149): Show | 154 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.102-6061T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587085 | ||||||
chr7:141587484
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.102-5662T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587484 | ||||||
chr7:141587584
|
C | T | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-5562C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587584 | ||||||
chr7:141587671
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.102-5475A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587671 | ||||||
chr7:141587729
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-5417A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587729 | ||||||
chr7:141587792
|
T | C | 10 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(7): Show | 11 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-5354T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587792 | ||||||
chr7:141587852
|
G | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.102-5294G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587852 | ||||||
chr7:141587949
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.102-5197A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587949 | ||||||
chr7:141588114
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.102-5032T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588114 | ||||||
chr7:141588135
|
A | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-5011A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588135 | ||||||
chr7:141588270
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.102-4876G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588270 | ||||||
chr7:141588617
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.102-4529G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588617 | ||||||
chr7:141588617
|
G | GA | 8 | a0001c0001t0001g0063a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-4516dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141588617 | |||||
chr7:141588966
|
G | A | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-4180G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588966 | ||||||
chr7:141589347
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-3799T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141589347 | ||||||
chr7:141589563
|
A | AT | 7 | a0001c0001t0001g0114a0001c0001t0001g0252a0001c0001t0001g0253others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-3569dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141589563 | |||||
chr7:141589749
|
G | A | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.102-3397G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141589749 | ||||||
chr7:141589751
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.102-3395G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141589751 | ||||||
chr7:141589787
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0048 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.102-3359C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141589787 | ||||||
chr7:141590271
|
T | C | 50 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(47): Show | 52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.102-2875T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590271 | ||||||
chr7:141590384
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | HG00735.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2762G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590384 | ||||||
chr7:141590457
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18977.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.102-2689G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590457 | ||||||
chr7:141590507
|
T | C | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-2639T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590507 | ||||||
chr7:141590518
|
G | A | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-2628G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590518 | ||||||
chr7:141590623
|
CTT | C | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.102-2521_102-2520d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141590623 | |||||
chr7:141590930
|
G | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-2216G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590930 | ||||||
chr7:141590953
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102-2193A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590953 | ||||||
chr7:141591058
|
T | A | 1 | a0001c0001t0001g0209 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.102-2088T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591058 | ||||||
chr7:141591082
|
G | GT | 15 | a0001c0001t0001g0020a0001c0001t0001g0057a0001c0001t0001g0102others(12): Show | 15 | HG00735.hp2 HG01952.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.102-2037dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591082 | |||||
chr7:141591082
|
GT | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(147): Show | 152 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.102-2037delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591082 | |||||
chr7:141591082
|
GTT | G | 10 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 11 | HG01346.hp1 HG01884.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-2038_102-2037d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591082 | |||||
chr7:141591082
|
GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 9 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-2049_102-2037d others(15): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591082 | |||||
chr7:141591083
|
T | A | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.102-2063T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591083 | ||||||
chr7:141591086
|
T | G | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2060T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591086 | ||||||
chr7:141591087
|
T | G | 1 | a0001c0001t0006g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.102-2059T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591087 | ||||||
chr7:141591088
|
T | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 7 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-2058T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591088 | ||||||
chr7:141591096
|
T | G | 1 | a0001c0001t0001g0064 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.102-2050T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591096 | ||||||
chr7:141591114
|
CAG | C | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.102-2029_102-2028d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591114 | |||||
chr7:141591323
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.102-1823C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591323 | ||||||
chr7:141591340
|
A | G | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1806A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591340 | ||||||
chr7:141591466
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.102-1680C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591466 | ||||||
chr7:141591610
|
T | G | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-1536T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591610 | ||||||
chr7:141591712
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102-1434C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591712 | ||||||
chr7:141591751
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.102-1395T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591751 | ||||||
chr7:141591826
|
G | A | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.102-1320G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591826 | ||||||
chr7:141592043
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.102-1103C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592043 | ||||||
chr7:141592273
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.102-873G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592273 | ||||||
chr7:141592345
|
T | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-801T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592345 | ||||||
chr7:141592613
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-533A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592613 | ||||||
chr7:141592641
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-505C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592641 | ||||||
chr7:141592743
|
G | A | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.102-403G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592743 | ||||||
chr7:141592746
|
C | T | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-400C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592746 | ||||||
chr7:141592964
|
AAAGTGCT others(10): Show |
A | 6 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(3): Show | 7 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-181_102-165del others(17): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592964 | ||||||
chr7:141593452
|
C | T | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+267C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141593452 | ||||||
chr7:141593617
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.141+432A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141593617 | ||||||
chr7:141593995
|
C | T | 1 | a0001c0001t0014g0006 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.141+810C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141593995 | ||||||
chr7:141594535
|
G | C | 4 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0232others(1): Show | 4 | HG01952.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+1350G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141594535 | ||||||
chr7:141594684
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.141+1499G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141594684 | ||||||
chr7:141594798
|
A | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.141+1613A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141594798 | ||||||
chr7:141594949
|
C | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-1613C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141594949 | ||||||
chr7:141595059
|
C | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142-1503C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595059 | ||||||
chr7:141595128
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-1434A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595128 | ||||||
chr7:141595258
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0106others(76): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.142-1304T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595258 | ||||||
chr7:141595371
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142-1191A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595371 | ||||||
chr7:141595669
|
A | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0222 | 2 | HG00408.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.142-893A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595669 | ||||||
chr7:141595811
|
C | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142-751C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595811 | ||||||
chr7:141596081
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.142-481C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141596081 | ||||||
chr7:141596670
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.221+29T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596670 | ||||||
chr7:141596749
|
A | G | 1 | a0001c0001t0017g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.221+108A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596749 | ||||||
chr7:141596848
|
G | A | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.221+207G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596848 | ||||||
chr7:141596921
|
C | T | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.221+280C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596921 | ||||||
chr7:141596929
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.221+288G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596929 | ||||||
chr7:141597735
|
G | A | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.221+1094G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141597735 | ||||||
chr7:141597876
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.221+1235G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141597876 | ||||||
chr7:141597890
|
C | CA | 16 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0050others(13): Show | 17 | HG00140.hp1 HG01192.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.221+1278dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141597890
|
CA | C | 20 | a0001c0001t0001g0095a0001c0001t0001g0104a0001c0001t0001g0108others(17): Show | 21 | HG00673.hp2 HG01255.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.221+1278delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141597890
|
CAA | C | 12 | a0001c0001t0001g0165a0001c0001t0001g0228a0001c0001t0001g0252others(9): Show | 12 | HG01099.hp2 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+1277_221+1278d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141597890
|
CAAA | C | 24 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0002g0229others(21): Show | 25 | HG00408.hp1 HG01261.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.221+1276_221+1278d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141597890
|
CAAAA | C | 6 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0263others(3): Show | 6 | HG01168.hp2 HG02486.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+1275_221+1278d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141597890
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0080others(2): Show | 5 | HG00673.hp1 HG01070.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+1268_221+1278d others(13): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141597890
|
CAAAAAAA others(5): Show |
C | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 73 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.221+1267_221+1278d others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141597890
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0079 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.221+1266_221+1278d others(15): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141597890
|
CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+1263_221+1278d others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | |||||
chr7:141598116
|
G | A | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.221+1475G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141598116 | ||||||
chr7:141598179
|
C | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0117a0001c0001t0001g0118others(8): Show | 12 | HG00140.hp1 HG01081.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+1538C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141598179 | ||||||
chr7:141598259
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0223 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.221+1618C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141598259 | ||||||
chr7:141598967
|
A | G | 10 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.222-2238A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141598967 | ||||||
chr7:141599061
|
A | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.222-2144A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599061 | ||||||
chr7:141599169
|
T | C | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.222-2036T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599169 | ||||||
chr7:141599172
|
C | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG02602.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.222-2033C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599172 | ||||||
chr7:141599233
|
T | A | 8 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0127others(5): Show | 8 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-1972T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599233 | ||||||
chr7:141599249
|
C | T | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.222-1956C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599249 | ||||||
chr7:141599271
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.222-1934G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599271 | ||||||
chr7:141599339
|
GCTAAAAG others(3): Show |
G | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.222-1861_222-1852d others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141599339 | |||||
chr7:141599371
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.222-1834G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599371 | ||||||
chr7:141599435
|
A | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.222-1770A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599435 | ||||||
chr7:141599527
|
A | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0144a0001c0001t0001g0218 | 3 | HG02572.hp1 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.222-1678A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599527 | ||||||
chr7:141599696
|
G | A | 7 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0127others(4): Show | 7 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-1509G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599696 | ||||||
chr7:141599865
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.222-1340C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599865 | ||||||
chr7:141600013
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.222-1192G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600013 | ||||||
chr7:141600099
|
T | C | 11 | a0001c0001t0001g0129a0001c0001t0001g0252a0001c0001t0001g0253others(8): Show | 12 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-1106T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600099 | ||||||
chr7:141600228
|
G | A | 1 | a0001c0001t0014g0006 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.222-977G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600228 | ||||||
chr7:141600239
|
A | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.222-966A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600239 | ||||||
chr7:141600270
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0207 | 2 | NA18957.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.222-935T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600270 | ||||||
chr7:141600696
|
A | G | 50 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(47): Show | 52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.222-509A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600696 | ||||||
chr7:141600811
|
T | C | 36 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(33): Show | 37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.222-394T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600811 | ||||||
chr7:141600957
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0184 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.222-248C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600957 | ||||||
chr7:141601077
|
T | C | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 9 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-128T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141601077 | ||||||
chr7:141601298
|
A | G | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.297+18A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141601298 | ||||||
chr7:141601404
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.297+124C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141601404 | ||||||
chr7:141601891
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.297+611T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141601891 | ||||||
chr7:141602033
|
C | CAT | 40 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(37): Show | 41 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.297+756_297+757dup others(2): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602033 | |||||
chr7:141602045
|
C | T | 4 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+765C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602045 | ||||||
chr7:141602073
|
A | G | 50 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(47): Show | 52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.297+793A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602073 | ||||||
chr7:141602172
|
C | CGTGTGT | 11 | a0001c0001t0002g0230a0001c0001t0002g0234a0001c0001t0002g0235others(8): Show | 11 | HG00408.hp1 HG02015.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(3): Show |
3 | a0001c0001t0002g0249a0001c0001t0003g0269a0001c0001t0004g0003 | 4 | HG03453.hp2 HG03540.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(5): Show |
9 | a0001c0001t0001g0228a0001c0001t0002g0229a0001c0001t0002g0231others(6): Show | 9 | HG01952.hp2 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(7): Show |
6 | a0001c0001t0001g0036a0001c0001t0002g0232a0001c0001t0003g0265others(3): Show | 6 | HG01884.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(9): Show |
3 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0004g0256 | 3 | HG02486.hp1 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.297+892_297+893ins others(16): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(11): Show |
3 | a0001c0001t0004g0254a0002c0002t0003g0004a0002c0002t0003g0270 | 4 | HG01261.hp1 HG02896.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(13): Show |
2 | a0001c0001t0002g0219a0001c0001t0003g0267 | 2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.297+892_297+893ins others(20): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(15): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0068 | 2 | HG01070.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.297+892_297+893ins others(22): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(21): Show |
1 | a0001c0001t0001g0083 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.297+892_297+893ins others(28): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(23): Show |
1 | a0001c0001t0001g0090 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.297+892_297+893ins others(30): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602172
|
C | CGTGTGTG others(25): Show |
1 | a0001c0001t0001g0091 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.297+892_297+893ins others(32): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | ||||||
chr7:141602173
|
T | G | 46 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0068others(43): Show | 48 | HG00408.hp1 HG01070.hp2 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.297+893T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602173 | ||||||
chr7:141602173
|
T | TGTGTGTG others(22): Show |
1 | a0001c0001t0001g0096 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.297+893_297+894ins others(29): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602173 | ||||||
chr7:141602173
|
T | TTG | 23 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0026others(20): Show | 23 | HG01070.hp1 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.297+931_297+932dup others(2): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTG | 6 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0163others(3): Show | 6 | HG01243.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+929_297+932dup others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(1): Show |
4 | a0001c0001t0001g0104a0001c0001t0001g0257a0001c0001t0001g0258others(1): Show | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+925_297+932dup others(8): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0006g0224a0001c0001t0006g0226 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.297+923_297+932dup others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(5): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0058others(1): Show | 4 | HG02109.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+921_297+932dup others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(7): Show |
6 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0031others(3): Show | 6 | HG02615.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+919_297+932dup others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(9): Show |
4 | a0001c0001t0001g0062a0001c0001t0001g0086a0001c0001t0001g0221others(1): Show | 4 | HG01081.hp1 HG01123.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+917_297+932dup others(16): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(11): Show |
7 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0065others(4): Show | 7 | HG00140.hp2 HG00423.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+915_297+932dup others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(13): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0038others(5): Show | 8 | HG01256.hp1 HG01361.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+913_297+932dup others(20): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(15): Show |
15 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0039others(12): Show | 15 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+911_297+932dup others(22): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(17): Show |
18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0023others(15): Show | 18 | HG00558.hp2 HG01168.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.297+909_297+932dup others(24): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(19): Show |
10 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0051others(7): Show | 10 | HG00597.hp2 HG00673.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.297+907_297+932dup others(26): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(21): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0045others(1): Show | 4 | HG02027.hp1 NA18954.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+905_297+932dup others(28): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(23): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0094 | 2 | NA19056.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.297+903_297+932dup others(30): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(27): Show |
1 | a0001c0001t0001g0075 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.297+899_297+932dup others(34): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(29): Show |
1 | a0001c0001t0001g0076 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.297+897_297+932dup others(36): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
T | TTGTGTGT others(31): Show |
1 | a0001c0001t0001g0077 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.297+895_297+932dup others(38): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602173
|
TTG | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0123others(3): Show | 6 | HG02080.hp1 HG02155.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+931_297+932del others(2): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | |||||
chr7:141602175
|
G | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.297+895G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602175 | ||||||
chr7:141602177
|
G | T | 1 | a0001c0001t0005g0262 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.297+897G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602177 | ||||||
chr7:141602213
|
A | G | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.297+933A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602213 | ||||||
chr7:141602301
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.297+1021C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602301 | ||||||
chr7:141602342
|
C | T | 36 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(33): Show | 37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.297+1062C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602342 | ||||||
chr7:141602369
|
A | C | 1 | a0001c0001t0001g0172 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.297+1089A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602369 | ||||||
chr7:141602786
|
T | C | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 9 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+1506T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602786 | ||||||
chr7:141602921
|
G | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0062others(5): Show | 8 | HG02040.hp1 NA18956.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+1641G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602921 | ||||||
chr7:141603121
|
A | G | 50 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(47): Show | 52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.297+1841A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603121 | ||||||
chr7:141603266
|
A | G | 4 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(1): Show | 5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+1986A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603266 | ||||||
chr7:141603346
|
T | C | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.297+2066T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603346 | ||||||
chr7:141603421
|
A | G | 10 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+2141A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603421 | ||||||
chr7:141603731
|
G | A | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.297+2451G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603731 | ||||||
chr7:141603890
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.297+2610C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603890 | ||||||
chr7:141604051
|
T | C | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.297+2771T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604051 | ||||||
chr7:141604310
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.297+3030C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604310 | ||||||
chr7:141604346
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+3066G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604346 | ||||||
chr7:141604372
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0058 | 2 | HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.297+3093_297+3094i others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604372 | |||||
chr7:141604374
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0052a0001c0001t0001g0058 | 3 | HG02717.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.297+3094G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604374 | ||||||
chr7:141604374
|
G | GTA | 30 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0107others(27): Show | 31 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.297+3123_297+3124d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTATA | 10 | a0001c0001t0001g0091a0001c0001t0001g0117a0001c0001t0001g0118others(7): Show | 10 | HG01081.hp2 HG01261.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+3121_297+3124d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTATATA | 24 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(21): Show | 24 | HG00140.hp2 HG00642.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+3119_297+3124d others(8): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTATATAT others(1): Show |
24 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(21): Show | 24 | HG00408.hp2 HG00544.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+3117_297+3124d others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTATATAT others(3): Show |
30 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(27): Show | 30 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.297+3115_297+3124d others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTATATAT others(5): Show |
8 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0063others(5): Show | 8 | HG00735.hp1 HG02148.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+3113_297+3124d others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTATATAT others(7): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0084others(4): Show | 7 | HG00423.hp2 HG01346.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+3111_297+3124d others(16): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTATATAT others(9): Show |
5 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0059others(2): Show | 5 | HG01099.hp1 HG02273.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+3109_297+3124d others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTGTA | 4 | a0001c0001t0004g0254a0001c0001t0004g0256a0002c0002t0003g0270others(1): Show | 4 | HG02896.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+3095_297+3096i others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTGTATA | 2 | a0001c0001t0001g0055a0002c0002t0003g0004 | 3 | HG01261.hp1 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.297+3095_297+3096i others(8): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTGTATAT others(1): Show |
4 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0096others(1): Show | 4 | HG01884.hp1 HG04204.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+3095_297+3096i others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0004g0003a0001c0001t0004g0255 | 3 | HG02630.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.297+3095_297+3096i others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTGTATAT others(5): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0252 | 2 | HG02970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.297+3095_297+3096i others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTGTATAT others(7): Show |
3 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG02896.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.297+3095_297+3096i others(16): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
G | GTGTGTAT others(17): Show |
1 | a0001c0001t0001g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.297+3095_297+3096i others(26): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
GTA | G | 13 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0155others(10): Show | 13 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.297+3123_297+3124d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
GTATA | G | 23 | a0001c0001t0001g0196a0001c0001t0002g0229a0001c0001t0002g0230others(20): Show | 23 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.297+3121_297+3124d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
GTATATAT others(3): Show |
G | 2 | a0001c0001t0001g0218a0001c0001t0006g0225 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.297+3115_297+3124d others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604374
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+3113_297+3124d others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | |||||
chr7:141604376
|
A | G | 9 | a0001c0001t0001g0190a0001c0001t0001g0212a0001c0001t0002g0219others(6): Show | 9 | HG02056.hp2 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+3096A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604376 | ||||||
chr7:141604378
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0002g0247 | 2 | HG02559.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.297+3098A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604378 | ||||||
chr7:141604380
|
A | G | 22 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(19): Show | 22 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.297+3100A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604380 | ||||||
chr7:141604382
|
A | G | 2 | a0001c0001t0002g0234a0004c0004t0002g0245 | 2 | NA18997.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.297+3102A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604382 | ||||||
chr7:141604384
|
A | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0226 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.297+3104A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604384 | ||||||
chr7:141604386
|
A | G | 1 | a0001c0001t0006g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.297+3106A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604386 | ||||||
chr7:141604394
|
A | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.297+3114A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604394 | ||||||
chr7:141604403
|
T | C | 13 | a0001c0001t0001g0169a0001c0001t0003g0265a0001c0001t0003g0266others(10): Show | 15 | HG01261.hp1 HG01884.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+3123T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604403 | ||||||
chr7:141604403
|
T | TATATATA others(9): Show |
1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.297+3124_297+3125i others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604403 | |||||
chr7:141604443
|
G | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0052others(4): Show | 7 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+3163G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604443 | ||||||
chr7:141604566
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.297+3286A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604566 | ||||||
chr7:141604582
|
A | AT | 5 | a0001c0001t0001g0198a0001c0001t0001g0228a0001c0001t0002g0235others(2): Show | 5 | HG02738.hp1 HG02922.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+3322dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604582 | |||||
chr7:141604582
|
A | ATT | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0268others(4): Show | 8 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+3321_297+3322d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604582 | |||||
chr7:141604582
|
AT | A | 12 | a0001c0001t0001g0036a0001c0001t0001g0079a0001c0001t0001g0102others(9): Show | 12 | HG01168.hp2 HG01256.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.297+3322delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604582 | |||||
chr7:141604622
|
T | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+3342T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604622 | ||||||
chr7:141604669
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+3389C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604669 | ||||||
chr7:141604984
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.297+3704C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604984 | ||||||
chr7:141605152
|
A | G | 36 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(33): Show | 37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.297+3872A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605152 | ||||||
chr7:141605168
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.297+3888G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605168 | ||||||
chr7:141605292
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.297+4012A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605292 | ||||||
chr7:141605848
|
T | C | 1 | a0001c0001t0015g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.297+4568T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605848 | ||||||
chr7:141605861
|
C | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+4581C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605861 | ||||||
chr7:141606011
|
G | A | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 147 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.297+4731G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606011 | ||||||
chr7:141606017
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+4737C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606017 | ||||||
chr7:141606495
|
T | A | 1 | a0001c0001t0002g0263 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.298-4700T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606495 | ||||||
chr7:141606502
|
A | G | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.298-4693A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606502 | ||||||
chr7:141606641
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.298-4554A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606641 | ||||||
chr7:141606723
|
G | T | 2 | a0001c0001t0009g0119a0001c0001t0009g0120 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.298-4472G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606723 | ||||||
chr7:141607303
|
C | T | 3 | a0001c0001t0003g0265a0002c0002t0003g0004a0002c0002t0003g0270 | 4 | HG01261.hp1 HG02896.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-3892C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607303 | ||||||
chr7:141607501
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0139 | 2 | HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.298-3694G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607501 | ||||||
chr7:141607658
|
T | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0095 | 3 | HG02735.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.298-3537T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607658 | ||||||
chr7:141607719
|
A | G | 3 | a0001c0001t0001g0171a0001c0001t0001g0202a0001c0001t0001g0205 | 3 | NA19000.hp2 NA19007.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.298-3476A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607719 | ||||||
chr7:141607817
|
T | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-3378T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607817 | ||||||
chr7:141607832
|
G | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-3363G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607832 | ||||||
chr7:141608108
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.298-3087C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608108 | ||||||
chr7:141608660
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.298-2535C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608660 | ||||||
chr7:141608728
|
C | T | 24 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(21): Show | 24 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-2467C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608728 | ||||||
chr7:141608767
|
C | T | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.298-2428C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608767 | ||||||
chr7:141608805
|
A | G | 50 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(47): Show | 52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.298-2390A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608805 | ||||||
chr7:141609245
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-1950C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609245 | ||||||
chr7:141609464
|
G | A | 45 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(42): Show | 47 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.298-1731G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609464 | ||||||
chr7:141609487
|
A | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-1708A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609487 | ||||||
chr7:141609604
|
A | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.298-1591A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609604 | ||||||
chr7:141609691
|
G | A | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-1504G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609691 | ||||||
chr7:141609759
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.298-1436G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609759 | ||||||
chr7:141609799
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0162 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.298-1396A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609799 | ||||||
chr7:141609868
|
G | A | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.298-1327G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609868 | ||||||
chr7:141609971
|
G | GT | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0032others(3): Show | 6 | HG02027.hp1 HG02922.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1212dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141609971 | |||||
chr7:141610102
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.298-1093A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610102 | ||||||
chr7:141610241
|
A | G | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-954A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610241 | ||||||
chr7:141610396
|
T | C | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.298-799T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610396 | ||||||
chr7:141610402
|
T | G | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.298-793T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610402 | ||||||
chr7:141610540
|
C | A | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-655C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610540 | ||||||
chr7:141610840
|
T | C | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.298-355T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610840 | ||||||
chr7:141611055
|
T | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.298-140T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141611055 | ||||||
chr7:141611089
|
G | A | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-106G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141611089 | ||||||
chr7:141612197
|
T | C | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.390+910T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612197 | ||||||
chr7:141612229
|
A | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.390+942A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612229 | ||||||
chr7:141612249
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0008g0033others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+962G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612249 | ||||||
chr7:141612297
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.390+1010C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612297 | ||||||
chr7:141612525
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.390+1238G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612525 | ||||||
chr7:141612557
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.390+1270A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612557 | ||||||
chr7:141612616
|
G | A | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1329G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612616 | ||||||
chr7:141612861
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.391-1285G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612861 | ||||||
chr7:141612906
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-1240A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612906 | ||||||
chr7:141612930
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.391-1216C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612930 | ||||||
chr7:141613123
|
T | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.391-1023T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613123 | ||||||
chr7:141613159
|
A | C | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-987A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613159 | ||||||
chr7:141613426
|
G | A | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-720G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613426 | ||||||
chr7:141613534
|
G | A | 4 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-612G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613534 | ||||||
chr7:141613619
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.391-527A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613619 | ||||||
chr7:141613797
|
A | G | 149 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(146): Show | 151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.391-349A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613797 | ||||||
chr7:141614087
|
C | A | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-59C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141614087 | ||||||
chr7:141614360
|
G | A | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+182G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | chr7 | 141614360 | ||||||
chr7:141614595
|
T | TTTCTACA others(320): Show |
1 | a0001c0001t0002g0263 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.423+429_423+430ins others(327): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | |||||
chr7:141614595
|
T | TTTCTACA others(314): Show |
1 | a0001c0001t0002g0247 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.423+431_423+432ins others(321): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | |||||
chr7:141614595
|
T | TTTCTACA others(315): Show |
6 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0240others(3): Show | 6 | HG02015.hp1 HG02155.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+431_423+432ins others(322): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | |||||
chr7:141614595
|
T | TTTCTACA others(316): Show |
13 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(10): Show | 13 | HG00408.hp1 HG01952.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.423+431_423+432ins others(323): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | |||||
chr7:141614595
|
T | TTTCTACA others(317): Show |
4 | a0001c0001t0002g0231a0001c0001t0002g0242a0001c0001t0002g0243others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+431_423+432ins others(324): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | |||||
chr7:141614596
|
T | A | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.423+418T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | chr7 | 141614596 | ||||||
chr7:141614791
|
CAT | C | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.423+616_423+617del others(2): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614791 | |||||
chr7:141614928
|
G | A | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-543G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | chr7 | 141614928 | ||||||
chr7:141615467
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.424-4C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | chr7 | 141615467 | ||||||
chr7:141615600
|
G | T | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.518+35G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141615600 | ||||||
chr7:141615645
|
TC | T | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+81delC | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141615645 | ||||||
chr7:141615874
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518+309A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141615874 | ||||||
chr7:141615919
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.518+354C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141615919 | ||||||
chr7:141616084
|
A | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.518+519A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616084 | ||||||
chr7:141616198
|
A | G | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.518+633A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616198 | ||||||
chr7:141616204
|
A | G | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.518+639A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616204 | ||||||
chr7:141616207
|
T | C | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.518+642T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616207 | ||||||
chr7:141616233
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG01081.hp1 HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.518+668A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616233 | ||||||
chr7:141616262
|
A | G | 3 | a0001c0001t0001g0171a0001c0001t0001g0202a0001c0001t0001g0205 | 3 | NA19000.hp2 NA19007.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.518+697A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616262 | ||||||
chr7:141616341
|
A | G | 1 | a0005c0005t0001g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.518+776A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616341 | ||||||
chr7:141616762
|
C | CT | 13 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG01070.hp2 HG01258.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.518+1211dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141616762 | |||||
chr7:141616805
|
C | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0162 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.518+1240C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616805 | ||||||
chr7:141616843
|
C | A | 1 | a0001c0001t0013g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.518+1278C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616843 | ||||||
chr7:141616853
|
G | A | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.518+1288G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616853 | ||||||
chr7:141616943
|
C | G | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.518+1378C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616943 | ||||||
chr7:141616999
|
C | T | 10 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.518+1434C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616999 | ||||||
chr7:141617034
|
C | T | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.518+1469C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141617034 | ||||||
chr7:141617585
|
T | G | 1 | a0001c0001t0002g0234 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.518+2020T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141617585 | ||||||
chr7:141618243
|
T | A | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.518+2678T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618243 | ||||||
chr7:141618441
|
G | A | 36 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(33): Show | 37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.518+2876G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618441 | ||||||
chr7:141618455
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.518+2890G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618455 | ||||||
chr7:141618705
|
A | G | 6 | a0001c0001t0001g0110a0001c0001t0001g0194a0001c0001t0001g0197others(3): Show | 6 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(3): Show |
intron_variant | MODIFIER | c.519-3027A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618705 | ||||||
chr7:141618827
|
C | T | 19 | a0001c0001t0002g0230a0001c0001t0002g0234a0001c0001t0002g0235others(16): Show | 19 | HG00408.hp1 HG02015.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.519-2905C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618827 | ||||||
chr7:141618890
|
G | A | 1 | a0001c0001t0005g0262 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.519-2842G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618890 | ||||||
chr7:141619115
|
T | G | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.519-2617T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619115 | ||||||
chr7:141619116
|
T | A | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.519-2616T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619116 | ||||||
chr7:141619149
|
T | A | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.519-2583T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619149 | ||||||
chr7:141619207
|
A | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.519-2525A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619207 | ||||||
chr7:141619222
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-2510G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619222 | ||||||
chr7:141619507
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-2225C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619507 | ||||||
chr7:141619643
|
A | G | 1 | a0001c0001t0002g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.519-2089A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619643 | ||||||
chr7:141619673
|
GA | G | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.519-2048delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141619673 | |||||
chr7:141619685
|
GCAAA | G | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.519-2042_519-2039d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141619685 | |||||
chr7:141619690
|
CAAA | C | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-2039_519-2037d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141619690 | |||||
chr7:141619754
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-1978G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619754 | ||||||
chr7:141619767
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.519-1965G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619767 | ||||||
chr7:141619888
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-1844G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619888 | ||||||
chr7:141619986
|
A | G | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.519-1746A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619986 | ||||||
chr7:141620063
|
G | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0223 | 2 | HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.519-1669G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620063 | ||||||
chr7:141620526
|
CAG | C | 97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.519-1205_519-1204d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620526 | ||||||
chr7:141620566
|
CTGGAAAC others(5): Show |
C | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.519-1144_519-1133d others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141620566 | |||||
chr7:141620729
|
TCCAGGAG others(5): Show |
T | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.519-991_519-980del others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141620729 | |||||
chr7:141620772
|
A | G | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-960A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620772 | ||||||
chr7:141620828
|
A | G | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.519-904A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620828 | ||||||
chr7:141620937
|
C | T | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.519-795C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620937 | ||||||
chr7:141620976
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.519-756G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620976 | ||||||
chr7:141621002
|
C | T | 10 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.519-730C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621002 | ||||||
chr7:141621050
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | NA18991.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.519-682C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621050 | ||||||
chr7:141621094
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.519-638A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621094 | ||||||
chr7:141621209
|
C | T | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.519-523C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621209 | ||||||
chr7:141621437
|
A | G | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519-295A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621437 | ||||||
chr7:141621634
|
ATG | A | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519-84_519-83delGT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141621634 | |||||
chr7:141622012
|
A | T | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.588+211A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141622012 | ||||||
chr7:141622237
|
C | T | 1 | a0001c0001t0004g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.588+436C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141622237 | ||||||
chr7:141622408
|
G | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0234 | 2 | NA18997.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.588+607G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141622408 | ||||||
chr7:141622818
|
G | T | 1 | a0001c0001t0015g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.588+1017G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141622818 | ||||||
chr7:141622918
|
T | TA | 34 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(31): Show | 35 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.588+1128dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141622918 | |||||
chr7:141623125
|
A | G | 7 | a0001c0001t0002g0235a0001c0001t0002g0237a0001c0001t0002g0238others(4): Show | 7 | HG00408.hp1 HG02155.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+1324A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623125 | ||||||
chr7:141623335
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.588+1534C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623335 | ||||||
chr7:141623336
|
G | A | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+1535G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623336 | ||||||
chr7:141623379
|
CA | C | 26 | a0001c0001t0001g0013a0001c0001t0001g0228a0001c0001t0002g0229others(23): Show | 28 | HG01168.hp2 HG01261.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.588+1591delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141623379 | |||||
chr7:141623391
|
AAGAAAAA others(10): Show |
A | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588+1592_588+1608d others(19): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141623391 | |||||
chr7:141623409
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588+1608A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623409 | ||||||
chr7:141623412
|
A | G | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.588+1611A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623412 | ||||||
chr7:141623413
|
A | T | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.588+1612A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623413 | ||||||
chr7:141623818
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.588+2017G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623818 | ||||||
chr7:141623825
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.588+2024C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623825 | ||||||
chr7:141623852
|
G | A | 10 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+2051G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623852 | ||||||
chr7:141624195
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.588+2394C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624195 | ||||||
chr7:141624437
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.588+2636T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624437 | ||||||
chr7:141624559
|
A | G | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2758A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624559 | ||||||
chr7:141624632
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.588+2831A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624632 | ||||||
chr7:141624694
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | NA18991.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.588+2893G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624694 | ||||||
chr7:141624923
|
C | T | 45 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(42): Show | 47 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.588+3122C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624923 | ||||||
chr7:141625108
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.588+3307T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625108 | ||||||
chr7:141625263
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.588+3462C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625263 | ||||||
chr7:141625542
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.588+3741A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625542 | ||||||
chr7:141625822
|
T | C | 36 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(33): Show | 37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.588+4021T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625822 | ||||||
chr7:141625847
|
T | G | 1 | a0001c0001t0001g0018 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.588+4046T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625847 | ||||||
chr7:141625899
|
G | A | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588+4098G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625899 | ||||||
chr7:141625918
|
G | C | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.588+4117G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625918 | ||||||
chr7:141626116
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.588+4315A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626116 | ||||||
chr7:141626137
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.588+4336A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626137 | ||||||
chr7:141626206
|
G | A | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588+4405G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626206 | ||||||
chr7:141626328
|
A | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.588+4527A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626328 | ||||||
chr7:141626482
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.588+4681A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626482 | ||||||
chr7:141626950
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.588+5149C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626950 | ||||||
chr7:141627003
|
A | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.588+5202A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627003 | ||||||
chr7:141627210
|
T | G | 10 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+5409T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627210 | ||||||
chr7:141627286
|
A | AT | 12 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0232others(9): Show | 13 | HG01261.hp1 HG01952.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.588+5494dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141627286 | |||||
chr7:141627367
|
T | C | 8 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0127others(5): Show | 8 | HG01261.hp2 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+5566T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627367 | ||||||
chr7:141627596
|
C | T | 10 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+5795C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627596 | ||||||
chr7:141627709
|
C | T | 7 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0127others(4): Show | 7 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+5908C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627709 | ||||||
chr7:141627769
|
A | C | 1 | a0001c0001t0001g0017 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.588+5968A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627769 | ||||||
chr7:141627856
|
A | T | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589-6045A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627856 | ||||||
chr7:141627967
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-5934C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627967 | ||||||
chr7:141628051
|
T | G | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.589-5850T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628051 | ||||||
chr7:141628183
|
G | T | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.589-5718G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628183 | ||||||
chr7:141628338
|
G | A | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.589-5563G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628338 | ||||||
chr7:141628673
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0082 | 2 | HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.589-5228C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628673 | ||||||
chr7:141628722
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-5179C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628722 | ||||||
chr7:141628965
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589-4936C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628965 | ||||||
chr7:141629845
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.589-4056T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141629845 | ||||||
chr7:141629851
|
T | C | 140 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 141 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.589-4050T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141629851 | ||||||
chr7:141629916
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.589-3985G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141629916 | ||||||
chr7:141630106
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.589-3795T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630106 | ||||||
chr7:141630167
|
G | T | 1 | a0002c0002t0003g0004 | 2 | HG01261.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.589-3734G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630167 | ||||||
chr7:141630379
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.589-3522C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630379 | ||||||
chr7:141630433
|
G | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.589-3468G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630433 | ||||||
chr7:141630534
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.589-3367A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630534 | ||||||
chr7:141630539
|
AAAT | A | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.589-3355_589-3353d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141630539 | |||||
chr7:141630938
|
G | T | 1 | a0002c0002t0003g0004 | 2 | HG01261.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.589-2963G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630938 | ||||||
chr7:141630999
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.589-2902A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630999 | ||||||
chr7:141631093
|
A | G | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2808A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631093 | ||||||
chr7:141631409
|
G | C | 10 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(7): Show | 11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-2492G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631409 | ||||||
chr7:141631527
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.589-2374C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631527 | ||||||
chr7:141631575
|
C | A | 1 | a0001c0001t0001g0207 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.589-2326C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631575 | ||||||
chr7:141631891
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.589-2010T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631891 | ||||||
chr7:141631954
|
T | C | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.589-1947T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631954 | ||||||
chr7:141632076
|
C | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02027.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.589-1825C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632076 | ||||||
chr7:141632187
|
T | C | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.589-1714T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632187 | ||||||
chr7:141632230
|
T | TA | 13 | a0001c0001t0001g0028a0001c0001t0001g0100a0001c0001t0001g0111others(10): Show | 13 | HG01361.hp2 HG01891.hp2 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-1657dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141632230 | |||||
chr7:141632230
|
TA | T | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.589-1657delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141632230 | |||||
chr7:141632245
|
CAAAA | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0165others(1): Show | 4 | HG01070.hp1 HG01099.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1651_589-1648d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141632245 | |||||
chr7:141632253
|
A | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.589-1648A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632253 | ||||||
chr7:141632435
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02027.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.589-1466T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632435 | ||||||
chr7:141632443
|
T | C | 4 | a0001c0001t0001g0228a0001c0001t0006g0224a0001c0001t0006g0225others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1458T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632443 | ||||||
chr7:141632930
|
G | A | 99 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(96): Show | 99 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.589-971G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632930 | ||||||
chr7:141633140
|
C | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.589-761C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633140 | ||||||
chr7:141633180
|
C | T | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.589-721C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633180 | ||||||
chr7:141633409
|
CACTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0228a0001c0001t0006g0224a0001c0001t0006g0225others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-484_589-472del others(13): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141633409 | |||||
chr7:141633458
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.589-443T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633458 | ||||||
chr7:141633553
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.589-348T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633553 | ||||||
chr7:141633635
|
A | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0056others(4): Show | 7 | HG00735.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-266A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633635 | ||||||
chr7:141634141
|
T | G | 1 | a0001c0001t0003g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.668+161T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634141 | ||||||
chr7:141634257
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.668+277G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634257 | ||||||
chr7:141634345
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.668+365G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634345 | ||||||
chr7:141634460
|
C | T | 2 | a0001c0001t0002g0230a0001c0001t0002g0234 | 2 | NA18997.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.668+480C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634460 | ||||||
chr7:141634730
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.668+750C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634730 | ||||||
chr7:141634738
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.668+758T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634738 | ||||||
chr7:141634830
|
C | CT | 12 | a0001c0001t0001g0074a0001c0001t0001g0108a0001c0001t0001g0178others(9): Show | 13 | HG01255.hp2 HG01261.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.668+865dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 141634830 | |||||
chr7:141634830
|
CT | C | 27 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0002g0219others(24): Show | 27 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.668+865delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 141634830 | |||||
chr7:141634990
|
ATGATTAT others(8): Show |
A | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.668+1011_668+1025d others(17): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634990 | ||||||
chr7:141635007
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.668+1027C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635007 | ||||||
chr7:141635096
|
C | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.668+1116C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635096 | ||||||
chr7:141635161
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01261.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.668+1181A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635161 | ||||||
chr7:141635186
|
G | A | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.668+1206G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635186 | ||||||
chr7:141635301
|
AATC | A | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1324_668+1326d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 141635301 | |||||
chr7:141635320
|
G | GTA | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.668+1341_668+1342d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 141635320 | |||||
chr7:141635526
|
C | A | 1 | a0001c0001t0001g0007 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.669-1434C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635526 | ||||||
chr7:141635550
|
C | T | 5 | a0001c0001t0001g0228a0001c0001t0006g0224a0001c0001t0006g0225others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-1410C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635550 | ||||||
chr7:141635603
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.669-1357A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635603 | ||||||
chr7:141635647
|
C | A | 1 | a0001c0001t0015g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.669-1313C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635647 | ||||||
chr7:141635671
|
T | C | 25 | a0001c0001t0001g0220a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.669-1289T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635671 | ||||||
chr7:141635885
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.669-1075A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635885 | ||||||
chr7:141635943
|
A | G | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.669-1017A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635943 | ||||||
chr7:141636516
|
G | A | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.669-444G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141636516 | ||||||
chr7:141636748
|
G | A | 34 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(31): Show | 35 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.669-212G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141636748 | ||||||
chr7:141636767
|
T | C | 1 | a0001c0001t0016g0170 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.669-193T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141636767 | ||||||
chr7:141637174
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 6 | HG00140.hp1 HG01192.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.726+157G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637174 | ||||||
chr7:141637204
|
T | C | 51 | a0001c0001t0001g0220a0001c0001t0001g0228a0001c0001t0001g0252others(48): Show | 53 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.726+187T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637204 | ||||||
chr7:141637279
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0126 | 2 | HG01496.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.726+262A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637279 | ||||||
chr7:141637430
|
G | A | 4 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(1): Show | 5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+413G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637430 | ||||||
chr7:141637725
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.726+708G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637725 | ||||||
chr7:141637767
|
T | C | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+750T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637767 | ||||||
chr7:141637853
|
A | G | 1 | a0001c0001t0006g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.726+836A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637853 | ||||||
chr7:141637965
|
GT | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0114others(7): Show | 10 | HG02083.hp1 NA18951.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+949delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637965 | ||||||
chr7:141638304
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.726+1287T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141638304 | ||||||
chr7:141638547
|
A | G | 40 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0229others(37): Show | 41 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.726+1530A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141638547 | ||||||
chr7:141638973
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG00544.hp2 NA18974.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.726+1956G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141638973 | ||||||
chr7:141639275
|
C | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.727-1973C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639275 | ||||||
chr7:141639404
|
G | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0135 | 2 | HG00735.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.727-1844G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639404 | ||||||
chr7:141639508
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.727-1740T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639508 | ||||||
chr7:141639807
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.727-1441C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639807 | ||||||
chr7:141639929
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.727-1319C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639929 | ||||||
chr7:141640003
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.727-1245A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640003 | ||||||
chr7:141640026
|
C | A | 1 | a0001c0001t0003g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.727-1222C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640026 | ||||||
chr7:141640245
|
A | G | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.727-1003A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640245 | ||||||
chr7:141640257
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.727-991C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640257 | ||||||
chr7:141640287
|
A | C | 5 | a0001c0001t0001g0228a0001c0001t0006g0224a0001c0001t0006g0225others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-961A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640287 | ||||||
chr7:141640307
|
T | TAGAAGCA others(11): Show |
2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.727-937_727-920dup others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr7 | 141640307 | |||||
chr7:141640476
|
G | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-772G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640476 | ||||||
chr7:141640518
|
C | A | 1 | a0001c0001t0007g0053 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.727-730C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640518 | ||||||
chr7:141640697
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.727-551G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640697 | ||||||
chr7:141640876
|
G | A | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.727-372G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640876 | ||||||
chr7:141640993
|
G | A | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.727-255G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640993 | ||||||
chr7:141641038
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.727-210G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141641038 | ||||||
chr7:141641577
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.877+179A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 12/15 | chr7 | 141641577 | ||||||
chr7:141641595
|
A | G | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.877+197A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 12/15 | chr7 | 141641595 | ||||||
chr7:141641706
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.878-105C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 12/15 | chr7 | 141641706 | ||||||
chr7:141641773
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.878-38A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 12/15 | chr7 | 141641773 | ||||||
chr7:141642129
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.975+221A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642129 | ||||||
chr7:141642170
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.975+262G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642170 | ||||||
chr7:141642343
|
T | G | 34 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(31): Show | 35 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.975+435T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642343 | ||||||
chr7:141642545
|
C | T | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.975+637C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642545 | ||||||
chr7:141642852
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0153 | 3 | HG00642.hp1 HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.975+944T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642852 | ||||||
chr7:141642959
|
A | G | 2 | a0001c0001t0002g0230a0001c0001t0002g0234 | 2 | NA18997.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.975+1051A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642959 | ||||||
chr7:141643222
|
C | T | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.975+1314C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643222 | ||||||
chr7:141643287
|
C | T | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.975+1379C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643287 | ||||||
chr7:141643417
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG00735.hp2 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.975+1509G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643417 | ||||||
chr7:141643594
|
C | T | 4 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(1): Show | 5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+1686C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643594 | ||||||
chr7:141643746
|
G | A | 24 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(21): Show | 24 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.975+1838G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643746 | ||||||
chr7:141644052
|
T | C | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.975+2144T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644052 | ||||||
chr7:141644091
|
T | C | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+2183T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644091 | ||||||
chr7:141644094
|
T | TA | 9 | a0001c0001t0001g0154a0001c0001t0001g0169a0001c0001t0001g0213others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.975+2199dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141644094 | |||||
chr7:141644094
|
TA | T | 99 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(96): Show | 99 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.975+2199delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141644094 | |||||
chr7:141644322
|
T | G | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.975+2414T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644322 | ||||||
chr7:141644418
|
A | G | 34 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(31): Show | 35 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.975+2510A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644418 | ||||||
chr7:141644730
|
A | G | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+2822A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644730 | ||||||
chr7:141644750
|
ATAAG | A | 5 | a0001c0001t0001g0228a0001c0001t0006g0224a0001c0001t0006g0225others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+2844_975+2847d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141644750 | |||||
chr7:141644946
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.975+3038A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644946 | ||||||
chr7:141644984
|
TATA | T | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.975+3081_975+3083d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141644984 | |||||
chr7:141644988
|
A | G | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268 | 3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.975+3080A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644988 | ||||||
chr7:141645072
|
T | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.975+3164T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141645072 | ||||||
chr7:141645566
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.975+3658G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141645566 | ||||||
chr7:141645587
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.976-3676C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141645587 | ||||||
chr7:141645863
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.976-3400G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141645863 | ||||||
chr7:141646176
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.976-3087A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646176 | ||||||
chr7:141646283
|
T | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0065a0001c0001t0001g0082others(2): Show | 5 | HG01346.hp1 HG02273.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.976-2980T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646283 | ||||||
chr7:141646372
|
CAATT | C | 4 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(1): Show | 5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-2889_976-2886d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141646372 | |||||
chr7:141646384
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.976-2879A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646384 | ||||||
chr7:141646427
|
A | G | 2 | a0001c0001t0008g0033a0001c0001t0008g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.976-2836A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646427 | ||||||
chr7:141646440
|
G | C | 50 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(47): Show | 52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.976-2823G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646440 | ||||||
chr7:141646645
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.976-2618T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646645 | ||||||
chr7:141646816
|
G | A | 4 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0185others(1): Show | 4 | HG00423.hp1 HG00597.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-2447G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646816 | ||||||
chr7:141646866
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.976-2397C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646866 | ||||||
chr7:141647158
|
A | T | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.976-2105A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647158 | ||||||
chr7:141647245
|
T | G | 2 | a0001c0001t0005g0261a0001c0001t0005g0262 | 2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.976-2018T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647245 | ||||||
chr7:141647298
|
T | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.976-1965T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647298 | ||||||
chr7:141647309
|
T | C | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-1954T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647309 | ||||||
chr7:141647367
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01261.hp2 HG02559.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.976-1896T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647367 | ||||||
chr7:141647423
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.976-1840C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647423 | ||||||
chr7:141647431
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.976-1832C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647431 | ||||||
chr7:141647733
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.976-1530C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647733 | ||||||
chr7:141647774
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.976-1489G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647774 | ||||||
chr7:141647829
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.976-1434C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647829 | ||||||
chr7:141647859
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.976-1404C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647859 | ||||||
chr7:141647873
|
G | A | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.976-1390G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647873 | ||||||
chr7:141647880
|
G | A | 27 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(24): Show | 27 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.976-1383G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647880 | ||||||
chr7:141648080
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.976-1183G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648080 | ||||||
chr7:141648127
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.976-1136G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648127 | ||||||
chr7:141648195
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.976-1068G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648195 | ||||||
chr7:141648517
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.976-746A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648517 | ||||||
chr7:141648579
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0049 | 2 | HG02080.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.976-684A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648579 | ||||||
chr7:141648595
|
A | G | 5 | a0001c0001t0004g0003a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-668A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648595 | ||||||
chr7:141648619
|
G | A | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.976-644G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648619 | ||||||
chr7:141648804
|
G | T | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.976-459G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648804 | ||||||
chr7:141649013
|
T | C | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.976-250T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141649013 | ||||||
chr7:141649094
|
G | GA | 12 | a0001c0001t0001g0020a0001c0001t0001g0084a0001c0001t0001g0109others(9): Show | 12 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.976-152dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141649094 | |||||
chr7:141649094
|
GA | G | 37 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0035others(34): Show | 37 | HG01952.hp2 HG02015.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.976-152delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141649094 | |||||
chr7:141649114
|
T | C | 50 | a0001c0001t0001g0228a0001c0001t0001g0252a0001c0001t0001g0253others(47): Show | 52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.976-149T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141649114 | ||||||
chr7:141649216
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.976-47T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141649216 | ||||||
chr7:141649483
|
T | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0079 | 3 | HG01943.hp1 HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1046+150T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649483 | ||||||
chr7:141649599
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1046+266G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649599 | ||||||
chr7:141649611
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1046+278G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649611 | ||||||
chr7:141649674
|
G | A | 2 | a0002c0002t0003g0004a0002c0002t0003g0270 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1046+341G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649674 | ||||||
chr7:141649703
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1046+370G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649703 | ||||||
chr7:141649734
|
T | C | 4 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+401T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649734 | ||||||
chr7:141649743
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1046+410T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649743 | ||||||
chr7:141649967
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1046+634C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649967 | ||||||
chr7:141650054
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1046+721T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650054 | ||||||
chr7:141650065
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1046+732G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650065 | ||||||
chr7:141650132
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1046+799C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650132 | ||||||
chr7:141650718
|
T | C | 1 | a0003c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1047-807T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650718 | ||||||
chr7:141650734
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1047-791C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650734 | ||||||
chr7:141650780
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1047-745C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650780 | ||||||
chr7:141650902
|
A | G | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1047-623A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650902 | ||||||
chr7:141650919
|
G | A | 1 | a0001c0001t0003g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1047-606G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650919 | ||||||
chr7:141650960
|
G | C | 9 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1047-565G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650960 | ||||||
chr7:141651170
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1047-355C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141651170 | ||||||
chr7:141651290
|
A | G | 25 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0001t0002g0230others(22): Show | 25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.1047-235A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141651290 | ||||||
chr7:141651467
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1047-58T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141651467 | ||||||
chr7:141652122
|
C | CG | 7 | a0001c0001t0001g0064a0001c0001t0001g0069a0001c0001t0001g0072others(4): Show | 7 | HG00558.hp2 HG01943.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131+515dupG | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr7 | 141652122 | |||||
chr7:141652122
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1131+513C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652122 | ||||||
chr7:141652189
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1131+580A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652189 | ||||||
chr7:141652229
|
G | A | 4 | a0001c0001t0001g0104a0001c0001t0001g0209a0001c0001t0001g0212others(1): Show | 4 | HG03225.hp1 NA18956.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132-558G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652229 | ||||||
chr7:141652304
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1132-483G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652304 | ||||||
chr7:141652308
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1132-479A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652308 | ||||||
chr7:141652747
|
T | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0032others(3): Show | 6 | HG02735.hp2 HG02738.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132-40T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652747 |