Item | Value |
---|---|
geneid | 10985 |
ensemblid | ENSG00000089154.11 |
hgncid | 4199 |
symbol | GCN1 |
name | GCN1 activator of EIF2AK4 |
refseq_nuc | NM_006836.2 |
refseq_prot | NP_006827.1 |
ensembl_nuc | ENST00000300648.7 |
ensembl_prot | ENSP00000300648.6 |
mane_status | MANE Select |
chr | chr12 |
start | 120127202 |
end | 120194715 |
strand | - |
ver | v1.2 |
region | chr12:120127202-120194715 |
region5000 | chr12:120122202-120199715 |
regionname0 | GCN1_chr12_120127202_120194715 |
regionname5000 | GCN1_chr12_120122202_120199715 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2671 | 287 | 78 | 50 | 118 | 8 | 31 | 86 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0002 | 0/0 | 2671 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0003 | 0/0 | 2671 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0004 | 0/0 | 2671 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0005 | 0/0 | 2671 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0006 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0007 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0008 | 0/0 | 2671 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0009 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0010 | 0/0 | 2671 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0011 | 0/0 | 2671 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0012 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0013 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0014 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0015 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0016 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 8016 | 113 | 18 | 10 | 71 | 2 | 11 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0002 | 0/0 | 8016 | 104 | 19 | 27 | 38 | 3 | 17 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0003 | 1/0 | 8016 | 18 | 0 | 9 | 3 | 3 | 2 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0004 | 0/0 | 8016 | 10 | 10 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0005 | 0/0 | 8016 | 8 | 6 | 0 | 1 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0006 | 0/0 | 8016 | 6 | 5 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0007 | 0/0 | 8016 | 5 | 5 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0008 | 0/0 | 8016 | 5 | 0 | 0 | 5 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0009 | 0/0 | 8016 | 5 | 4 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0010 | 0/0 | 8016 | 4 | 0 | 0 | 4 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0011 | 0/0 | 8016 | 4 | 3 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0012 | 0/0 | 8016 | 3 | 0 | 0 | 3 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0013 | 0/0 | 8016 | 3 | 3 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0014 | 0/0 | 8016 | 2 | 2 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0015 | 0/0 | 8016 | 2 | 1 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0016 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0017 | 0/0 | 8016 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0018 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0019 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0020 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0021 | 0/0 | 8016 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0022 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0023 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0024 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0025 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0026 | 0/0 | 8016 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0027 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0028 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0029 | 0/0 | 8016 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0030 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0031 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0032 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0033 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0034 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
c0035 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 666 | 166 | 43 | 21 | 79 | 5 | 16 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
t0002 | 0/0 | 666 | 143 | 41 | 29 | 52 | 5 | 16 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
t0003 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
t0004 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
t0005 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 8016 | 113 | 18 | 10 | 71 | 2 | 11 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0002 | 0/0 | 8016 | 104 | 19 | 27 | 38 | 3 | 17 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0003 | 1/0 | 8016 | 18 | 0 | 9 | 3 | 3 | 2 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0004 | 0/0 | 8016 | 10 | 10 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0005 | 0/0 | 8016 | 8 | 6 | 0 | 1 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0006 | 0/0 | 8016 | 6 | 5 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0007 | 0/0 | 8016 | 5 | 5 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0009 | 0/0 | 8016 | 5 | 4 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0011 | 0/0 | 8016 | 4 | 3 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0012 | 0/0 | 8016 | 3 | 0 | 0 | 3 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0014 | 0/0 | 8016 | 2 | 2 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0016 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0017 | 0/0 | 8016 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0018 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0020 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0022 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0025 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0030 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0031 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0001c0035 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0002c0008 | 0/0 | 8016 | 5 | 0 | 0 | 5 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0003c0010 | 0/0 | 8016 | 4 | 0 | 0 | 4 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0004c0013 | 0/0 | 8016 | 3 | 3 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0005c0015 | 0/0 | 8016 | 2 | 1 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0006c0033 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0007c0019 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0008c0021 | 0/0 | 8016 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0009c0027 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0010c0026 | 0/0 | 8016 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0011c0029 | 0/0 | 8016 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0012c0028 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0013c0024 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0014c0023 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0015c0032 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 | |
a0016c0034 | 0/0 | 8016 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 8681 | 111 | 18 | 10 | 69 | 2 | 11 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0001t0002 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0001t0005 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0002t0001 | 0/0 | 8681 | 4 | 1 | 2 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0002t0002 | 0/0 | 8681 | 100 | 18 | 25 | 38 | 3 | 16 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0003t0001 | 1/0 | 8681 | 16 | 0 | 8 | 3 | 2 | 2 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0003t0002 | 0/0 | 8681 | 2 | 0 | 1 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0004t0001 | 0/0 | 8681 | 9 | 9 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0004t0003 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0005t0001 | 0/0 | 8681 | 2 | 0 | 0 | 1 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0005t0002 | 0/0 | 8681 | 6 | 6 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0006t0002 | 0/0 | 8681 | 6 | 5 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0007t0002 | 0/0 | 8681 | 5 | 5 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0009t0002 | 0/0 | 8681 | 5 | 4 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0011t0001 | 0/0 | 8681 | 4 | 3 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0012t0001 | 0/0 | 8681 | 3 | 0 | 0 | 3 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0014t0001 | 0/0 | 8681 | 2 | 2 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0016t0001 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0017t0002 | 0/0 | 8681 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0018t0001 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0020t0001 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0022t0001 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0025t0001 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0030t0001 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0031t0002 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0001c0035t0002 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0002c0008t0002 | 0/0 | 8681 | 5 | 0 | 0 | 5 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0003c0010t0002 | 0/0 | 8681 | 4 | 0 | 0 | 4 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0004c0013t0001 | 0/0 | 8681 | 3 | 3 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0005c0015t0002 | 0/0 | 8681 | 2 | 1 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0006c0033t0004 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0007c0019t0001 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0008c0021t0001 | 0/0 | 8681 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0009c0027t0002 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0010c0026t0002 | 0/0 | 8681 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0011c0029t0001 | 0/0 | 8681 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0012c0028t0002 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0013c0024t0001 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0014c0023t0001 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0015c0032t0001 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
a0016c0034t0002 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | copy fasta | chr12 | 120122202 | 120199715 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0004t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0005t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0005t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0005t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0005t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0005t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0005t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0006t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0006t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0006t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0006t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0006t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0006t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0007t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0007t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0007t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0007t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0007t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0009t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0009t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0009t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0009t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0009t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0011t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0011t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0011t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0011t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0012t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0012t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0012t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0014t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0014t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0016t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0017t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0018t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0020t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0022t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0025t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0030t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0031t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0001c0035t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0002c0008t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0002c0008t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0002c0008t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0002c0008t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0003c0010t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0003c0010t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0003c0010t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0003c0010t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0004c0013t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0004c0013t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0004c0013t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0005c0015t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0005c0015t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0006c0033t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0007c0019t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0008c0021t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0009c0027t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0010c0026t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0011c0029t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0012c0028t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0013c0024t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0014c0023t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0015c0032t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
a0016c0034t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0189 | EUR | GBR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0007 | EUR | GBR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00140 | hp2 | a0011 | c0029 | t0001 | g0042 | EUR | GBR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00280 | hp1 | a0001 | c0003 | t0002 | g0115 | EUR | FIN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0003 | EUR | FIN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0118 | EUR | FIN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00323 | hp2 | a0010 | c0026 | t0002 | g0062 | EUR | FIN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00438 | hp2 | a0001 | c0005 | t0001 | g0092 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00609 | hp2 | a0002 | c0008 | t0002 | g0195 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0051 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | CHS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0050 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0041 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0139 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01099 | hp1 | a0001 | c0011 | t0001 | g0231 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01106 | hp1 | a0001 | c0017 | t0002 | g0174 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0054 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01109 | hp2 | a0001 | c0009 | t0002 | g0028 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0052 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01169 | hp1 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0037 | AMR | CLM | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0159 | AMR | CLM | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0073 | AMR | CLM | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0044 | EUR | IBS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01884 | hp1 | a0013 | c0024 | t0001 | g0297 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01891 | hp1 | a0001 | c0014 | t0001 | g0080 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0067 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0134 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01943 | hp2 | a0001 | c0006 | t0002 | g0019 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0146 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0063 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02055 | hp1 | a0001 | c0009 | t0002 | g0016 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02132 | hp2 | a0009 | c0027 | t0002 | g0165 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02155 | hp1 | a0002 | c0008 | t0002 | g0006 | EAS | CDX | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02257 | hp1 | a0015 | c0032 | t0001 | g0113 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02257 | hp2 | a0001 | c0025 | t0001 | g0083 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02258 | hp1 | a0001 | c0009 | t0002 | g0026 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02280 | hp1 | a0001 | c0007 | t0002 | g0192 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02280 | hp2 | a0001 | c0004 | t0001 | g0084 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0047 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0168 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | PEL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02451 | hp1 | a0001 | c0004 | t0001 | g0086 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02523 | hp1 | a0014 | c0023 | t0001 | g0222 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | KHV | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02572 | hp1 | a0001 | c0011 | t0001 | g0249 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02572 | hp2 | a0001 | c0006 | t0002 | g0022 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0156 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02630 | hp1 | a0001 | c0018 | t0001 | g0032 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02630 | hp2 | a0004 | c0013 | t0001 | g0104 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0132 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0082 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02723 | hp1 | a0004 | c0013 | t0001 | g0098 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02723 | hp2 | a0001 | c0030 | t0001 | g0033 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0152 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0188 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0122 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02809 | hp1 | a0001 | c0011 | t0001 | g0247 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02809 | hp2 | a0001 | c0006 | t0002 | g0020 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02818 | hp2 | a0001 | c0011 | t0001 | g0248 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02886 | hp1 | a0004 | c0013 | t0001 | g0103 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0027 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0059 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0076 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0018 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02965 | hp1 | a0001 | c0004 | t0003 | g0031 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02976 | hp1 | a0001 | c0014 | t0001 | g0079 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0148 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03041 | hp1 | a0001 | c0006 | t0002 | g0017 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03041 | hp2 | a0006 | c0033 | t0004 | g0107 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03098 | hp1 | a0001 | c0006 | t0002 | g0023 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03098 | hp2 | a0001 | c0007 | t0002 | g0140 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03139 | hp1 | a0005 | c0015 | t0002 | g0180 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03139 | hp2 | a0001 | c0007 | t0002 | g0136 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03225 | hp2 | a0001 | c0006 | t0002 | g0021 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0087 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03486 | hp1 | a0001 | c0020 | t0001 | g0096 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03486 | hp2 | a0001 | c0007 | t0002 | g0078 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03540 | hp1 | a0001 | c0005 | t0002 | g0036 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0126 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0184 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | STU | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0142 | SAS | BEB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03927 | hp1 | a0001 | c0005 | t0001 | g0093 | SAS | BEB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03927 | hp2 | a0008 | c0021 | t0001 | g0276 | SAS | BEB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | STU | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0121 | SAS | STU | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0088 | AFR | YRI | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | YRI | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18942 | hp1 | a0002 | c0008 | t0002 | g0193 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18948 | hp2 | a0001 | c0012 | t0001 | g0221 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18962 | hp1 | a0016 | c0034 | t0002 | g0147 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18966 | hp1 | a0003 | c0010 | t0002 | g0123 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18973 | hp1 | a0003 | c0010 | t0002 | g0157 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18979 | hp2 | a0007 | c0019 | t0001 | g0239 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18984 | hp2 | a0001 | c0035 | t0002 | g0124 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18985 | hp1 | a0002 | c0008 | t0002 | g0006 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18997 | hp1 | a0002 | c0008 | t0002 | g0194 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18997 | hp2 | a0001 | c0012 | t0001 | g0282 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA18999 | hp2 | a0005 | c0015 | t0002 | g0143 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19005 | hp2 | a0001 | c0012 | t0001 | g0224 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19011 | hp2 | a0003 | c0010 | t0002 | g0178 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19030 | hp1 | a0001 | c0005 | t0002 | g0057 | AFR | LWK | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0085 | AFR | LWK | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | LWK | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | LWK | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19056 | hp1 | a0003 | c0010 | t0002 | g0137 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19068 | hp1 | a0001 | c0022 | t0001 | g0268 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | YRI | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA19240 | hp2 | a0001 | c0031 | t0002 | g0030 | AFR | YRI | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA20129 | hp1 | a0012 | c0028 | t0002 | g0175 | AFR | ASW | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | ASW | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | GIH | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | GIH | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02109 | hp1 | a0001 | c0007 | t0002 | g0141 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02109 | hp2 | a0001 | c0009 | t0002 | g0024 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02486 | hp1 | a0001 | c0005 | t0002 | g0039 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0081 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02559 | hp1 | a0001 | c0005 | t0002 | g0038 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG02559 | hp2 | a0001 | c0009 | t0002 | g0025 | AFR | ACB | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03471 | hp1 | a0001 | c0016 | t0001 | g0015 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG03471 | hp2 | a0001 | c0005 | t0002 | g0056 | AFR | MSL | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | USA | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
HG06807 | hp2 | a0001 | c0005 | t0002 | g0060 | AFR | USA | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0258 | REF | REF | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0045 | REF | REF | GCN1_chr12_120122202_120199715 | GCN1 | chr12 | 120122202 | 120199715 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120131328 | C | T | 1 | a0005 | 2 | HG03139.hp1 NA18999.hp2 |
missense_variant | MODERATE | c.7420G>A | p.Val2474Met | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 55/58 | 7438/8681 | 7420/8016 | 2474/2671 | chr12 | 120131328 | ||
chr12:120137277 | G | A | 1 | a0010 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.6706C>T | p.His2236Tyr | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/58 | 6724/8681 | 6706/8016 | 2236/2671 | chr12 | 120137277 | ||
chr12:120137603 | T | C | 1 | a0006 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.6605A>G | p.Asn2202Ser | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 49/58 | 6623/8681 | 6605/8016 | 2202/2671 | chr12 | 120137603 | ||
chr12:120137727 | G | A | 1 | a0009 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.6481C>T | p.Arg2161Cys | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 49/58 | 6499/8681 | 6481/8016 | 2161/2671 | chr12 | 120137727 | ||
chr12:120137745 | C | A | 1 | a0011 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.6463G>T | p.Asp2155Tyr | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 49/58 | 6481/8681 | 6463/8016 | 2155/2671 | chr12 | 120137745 | ||
chr12:120137749 | G | C | 2 | a0003a0016 | 5 | NA18962.hp1 NA18966.hp1 NA18973.hp1 others(2): Show |
missense_variant | MODERATE | c.6459C>G | p.Ile2153Met | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 49/58 | 6477/8681 | 6459/8016 | 2153/2671 | chr12 | 120137749 | ||
chr12:120142628 | G | A | 1 | a0012 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.5708C>T | p.Ala1903Val | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/58 | 5726/8681 | 5708/8016 | 1903/2671 | chr12 | 120142628 | ||
chr12:120148316 | T | A | 1 | a0008 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.4577A>T | p.Tyr1526Phe | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 37/58 | 4595/8681 | 4577/8016 | 1526/2671 | chr12 | 120148316 | ||
chr12:120153866 | C | T | 1 | a0013 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.3745G>A | p.Asp1249Asn | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 32/58 | 3763/8681 | 3745/8016 | 1249/2671 | chr12 | 120153866 | ||
chr12:120155305 | C | T | 1 | a0007 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.3566G>A | p.Arg1189His | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 30/58 | 3584/8681 | 3566/8016 | 1189/2671 | chr12 | 120155305 | ||
chr12:120155701 | T | C | 1 | a0014 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.3331A>G | p.Met1111Val | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 29/58 | 3349/8681 | 3331/8016 | 1111/2671 | chr12 | 120155701 | ||
chr12:120157874 | T | C | 1 | a0015 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.3062A>G | p.Asn1021Ser | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/58 | 3080/8681 | 3062/8016 | 1021/2671 | chr12 | 120157874 | ||
chr12:120159926 | G | C | 1 | a0006 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.2648C>G | p.Ser883Cys | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/58 | 2666/8681 | 2648/8016 | 883/2671 | chr12 | 120159926 | ||
chr12:120163210 | G | A | 1 | a0002 | 5 | HG00609.hp2 HG02155.hp1 NA18942.hp1 others(2): Show |
missense_variant | MODERATE | c.1898C>T | p.Ala633Val | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 19/58 | 1916/8681 | 1898/8016 | 633/2671 | chr12 | 120163210 | ||
chr12:120170210 | G | C | 1 | a0016 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.1478C>G | p.Ala493Gly | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/58 | 1496/8681 | 1478/8016 | 493/2671 | chr12 | 120170210 | ||
chr12:120175790 | G | A | 1 | a0004 | 3 | HG02630.hp2 HG02723.hp1 HG02886.hp1 |
missense_variant | MODERATE | c.998C>T | p.Ser333Leu | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 11/58 | 1016/8681 | 998/8016 | 333/2671 | chr12 | 120175790 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120137251 | G | A | 1 | a0001c0031 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.6732C>T | p.Asn2244Asn | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/58 | 6750/8681 | 6732/8016 | 2244/2671 | chr12 | 120137251 | ||
chr12:120137596 | G | A | 2 | a0001c0007a0001c0031 | 6 | HG02109.hp1 HG02280.hp1 HG03098.hp2 others(3): Show |
synonymous_variant | LOW | c.6612C>T | p.Ser2204Ser | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 49/58 | 6630/8681 | 6612/8016 | 2204/2671 | chr12 | 120137596 | ||
chr12:120138833 | G | A | 1 | a0001c0020 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.6018C>T | p.Leu2006Leu | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 46/58 | 6036/8681 | 6018/8016 | 2006/2671 | chr12 | 120138833 | ||
chr12:120142519 | T | C | 2 | a0001c0006a0001c0009 | 11 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(8): Show |
synonymous_variant | LOW | c.5817A>G | p.Ala1939Ala | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/58 | 5835/8681 | 5817/8016 | 1939/2671 | chr12 | 120142519 | ||
chr12:120142588 | G | C | 1 | a0001c0025 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.5748C>G | p.Pro1916Pro | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/58 | 5766/8681 | 5748/8016 | 1916/2671 | chr12 | 120142588 | ||
chr12:120144810 | C | T | 2 | a0001c0014a0001c0031 | 3 | HG01891.hp1 HG02976.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.5181G>A | p.Leu1727Leu | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 41/58 | 5199/8681 | 5181/8016 | 1727/2671 | chr12 | 120144810 | ||
chr12:120148189 | A | G | 2 | a0001c0014a0001c0031 | 3 | HG01891.hp1 HG02976.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.4704T>C | p.Val1568Val | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 37/58 | 4722/8681 | 4704/8016 | 1568/2671 | chr12 | 120148189 | ||
chr12:120151260 | G | C | 20 | a0001c0001a0001c0004a0001c0005others(17): Show | 163 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
synonymous_variant | LOW | c.4194C>G | p.Ala1398Ala | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/58 | 4212/8681 | 4194/8016 | 1398/2671 | chr12 | 120151260 | ||
chr12:120151356 | A | G | 33 | a0001c0001a0001c0002a0001c0004others(30): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
synonymous_variant | LOW | c.4098T>C | p.Leu1366Leu | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/58 | 4116/8681 | 4098/8016 | 1366/2671 | chr12 | 120151356 | ||
chr12:120153339 | A | G | 15 | a0001c0001a0001c0004a0001c0011others(12): Show | 144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
synonymous_variant | LOW | c.3936T>C | p.Tyr1312Tyr | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/58 | 3954/8681 | 3936/8016 | 1312/2671 | chr12 | 120153339 | ||
chr12:120155241 | G | A | 1 | a0001c0031 | 1 | NA19240.hp2 | splice_region_variant&synonymous_variant | LOW | c.3630C>T | p.Tyr1210Tyr | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 30/58 | 3648/8681 | 3630/8016 | 1210/2671 | chr12 | 120155241 | ||
chr12:120155268 | G | A | 1 | a0001c0030 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.3603C>T | p.Leu1201Leu | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 30/58 | 3621/8681 | 3603/8016 | 1201/2671 | chr12 | 120155268 | ||
chr12:120155331 | G | A | 1 | a0001c0031 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.3540C>T | p.Ala1180Ala | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 30/58 | 3558/8681 | 3540/8016 | 1180/2671 | chr12 | 120155331 | ||
chr12:120159915 | A | G | 1 | a0013c0024 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.2659T>C | p.Leu887Leu | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/58 | 2677/8681 | 2659/8016 | 887/2671 | chr12 | 120159915 | ||
chr12:120170227 | A | G | 9 | a0001c0001a0001c0011a0001c0012others(6): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
synonymous_variant | LOW | c.1461T>C | p.Thr487Thr | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/58 | 1479/8681 | 1461/8016 | 487/2671 | chr12 | 120170227 | ||
chr12:120170263 | C | T | 1 | a0001c0018 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1425G>A | p.Lys475Lys | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/58 | 1443/8681 | 1425/8016 | 475/2671 | chr12 | 120170263 | ||
chr12:120175193 | A | G | 1 | a0001c0017 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.1062T>C | p.Thr354Thr | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/58 | 1080/8681 | 1062/8016 | 354/2671 | chr12 | 120175193 | ||
chr12:120177538 | C | A | 1 | a0001c0035 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.747G>T | p.Leu249Leu | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/58 | 765/8681 | 747/8016 | 249/2671 | chr12 | 120177538 | ||
chr12:120177732 | G | A | 1 | a0001c0011 | 4 | HG01099.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.681C>T | p.Tyr227Tyr | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 8/58 | 699/8681 | 681/8016 | 227/2671 | chr12 | 120177732 | ||
chr12:120178643 | G | A | 1 | a0001c0009 | 5 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
synonymous_variant | LOW | c.642C>T | p.Asp214Asp | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 7/58 | 660/8681 | 642/8016 | 214/2671 | chr12 | 120178643 | ||
chr12:120190317 | C | T | 1 | a0001c0016 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.102G>A | p.Gly34Gly | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/58 | 120/8681 | 102/8016 | 34/2671 | chr12 | 120190317 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120127384 | G | A | 17 | a0001c0001t0002a0001c0002t0002a0001c0003t0002others(14): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*465C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 58/58 | 465 | chr12 | 120127384 | |||||
chr12:120127695 | G | T | 1 | a0006c0033t0004 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*154C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 58/58 | 154 | chr12 | 120127695 | |||||
chr12:120127719 | G | A | 1 | a0001c0001t0005 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*130C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 58/58 | 130 | chr12 | 120127719 | |||||
chr12:120127750 | C | T | 1 | a0001c0004t0003 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*99G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 58/58 | 99 | chr12 | 120127750 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120128026 | C | T | 11 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.7891-52G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128026 | ||||||
chr12:120128069 | A | G | 1 | a0001c0002t0002g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.7891-95T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128069 | ||||||
chr12:120128074 | G | C | 2 | a0001c0001t0001g0223a0014c0023t0001g0222 | 2 | HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.7891-100C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128074 | ||||||
chr12:120128200 | G | A | 11 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.7891-226C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128200 | ||||||
chr12:120128292 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.7891-318T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128292 | ||||||
chr12:120128559 | C | T | 1 | a0001c0003t0002g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.7891-585G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128559 | ||||||
chr12:120128574 | G | C | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7891-600C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128574 | ||||||
chr12:120128583 | A | G | 2 | a0001c0002t0002g0066a0001c0031t0002g0030 | 2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7891-609T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128583 | ||||||
chr12:120128775 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7890+501G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128775 | ||||||
chr12:120128806 | T | C | 1 | a0001c0002t0002g0158 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.7890+470A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128806 | ||||||
chr12:120128834 | A | C | 3 | a0001c0001t0001g0283a0001c0002t0002g0058a0001c0002t0002g0059 | 3 | HG02886.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.7890+442T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128834 | ||||||
chr12:120128837 | C | CT | 65 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0202others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.7890+438dupA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128837 | ||||||
chr12:120128837 | C | CTT | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 90 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.7890+437_7890+438d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128837 | ||||||
chr12:120128837 | C | CTTT | 9 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0106others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.7890+436_7890+438d others(5): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128837 | ||||||
chr12:120128837 | CT | C | 7 | a0001c0001t0001g0278a0001c0002t0002g0007a0001c0002t0002g0091others(4): Show | 8 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.7890+438delA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120128837 | ||||||
chr12:120129029 | G | A | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7890+247C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120129029 | ||||||
chr12:120129156 | T | C | 1 | a0001c0005t0001g0092 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.7890+120A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 57/57 | chr12 | 120129156 | ||||||
chr12:120129599 | C | T | 1 | a0007c0019t0001g0239 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.7672-105G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120129599 | ||||||
chr12:120129602 | C | A | 87 | a0001c0001t0001g0215a0001c0002t0002g0002a0001c0002t0002g0007others(84): Show | 91 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.7672-108G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120129602 | ||||||
chr12:120129762 | T | G | 1 | a0001c0004t0003g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7672-268A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120129762 | ||||||
chr12:120129779 | C | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0207others(12): Show | 17 | HG01934.hp1 HG02004.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.7672-285G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120129779 | ||||||
chr12:120129780 | G | A | 2 | a0001c0002t0001g0035a0001c0002t0001g0130 | 2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.7672-286C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120129780 | ||||||
chr12:120129996 | C | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0209others(23): Show | 27 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.7672-502G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120129996 | ||||||
chr12:120130031 | G | C | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7672-537C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130031 | ||||||
chr12:120130031 | G | T | 1 | a0001c0018t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7672-537C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130031 | ||||||
chr12:120130093 | A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.7671+553T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130093 | ||||||
chr12:120130099 | T | C | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7671+547A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130099 | ||||||
chr12:120130148 | A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(292): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.7671+498T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130148 | ||||||
chr12:120130228 | C | T | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7671+418G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130228 | ||||||
chr12:120130370 | G | A | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.7671+276C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130370 | ||||||
chr12:120130431 | T | G | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7671+215A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130431 | ||||||
chr12:120130533 | C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.7671+113G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 56/57 | chr12 | 120130533 | ||||||
chr12:120130807 | C | T | 2 | a0001c0002t0002g0122a0001c0002t0002g0152 | 2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.7564-54G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 55/57 | chr12 | 120130807 | ||||||
chr12:120130936 | A | C | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7564-183T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 55/57 | chr12 | 120130936 | ||||||
chr12:120131076 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.7563+109A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 55/57 | chr12 | 120131076 | ||||||
chr12:120131116 | C | T | 16 | a0001c0001t0001g0101a0001c0004t0001g0018a0001c0004t0001g0027others(13): Show | 16 | HG00438.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.7563+69G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 55/57 | chr12 | 120131116 | ||||||
chr12:120131144 | G | A | 1 | a0001c0002t0002g0191 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.7563+41C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 55/57 | chr12 | 120131144 | ||||||
chr12:120131365 | G | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7415-32C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 54/57 | chr12 | 120131365 | ||||||
chr12:120131382 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.7415-49G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 54/57 | chr12 | 120131382 | ||||||
chr12:120131472 | G | T | 1 | a0001c0001t0001g0278 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.7415-139C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 54/57 | chr12 | 120131472 | ||||||
chr12:120131538 | T | C | 1 | a0001c0003t0001g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.7415-205A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 54/57 | chr12 | 120131538 | ||||||
chr12:120131551 | C | T | 4 | a0001c0005t0002g0036a0001c0005t0002g0038a0001c0005t0002g0039others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.7415-218G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 54/57 | chr12 | 120131551 | ||||||
chr12:120131672 | G | C | 2 | a0006c0033t0004g0107a0013c0024t0001g0297 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.7414+254C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 54/57 | chr12 | 120131672 | ||||||
chr12:120131863 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7414+63C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 54/57 | chr12 | 120131863 | ||||||
chr12:120131874 | G | C | 1 | a0001c0002t0002g0182 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7414+52C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 54/57 | chr12 | 120131874 | ||||||
chr12:120132058 | G | A | 1 | a0001c0002t0002g0197 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.7318-36C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132058 | ||||||
chr12:120132134 | A | C | 1 | a0001c0001t0001g0266 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.7318-112T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132134 | ||||||
chr12:120132194 | T | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0001g0210others(21): Show | 25 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.7318-172A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132194 | ||||||
chr12:120132210 | A | G | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7318-188T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132210 | ||||||
chr12:120132288 | T | C | 3 | a0001c0005t0001g0092a0001c0005t0001g0093a0001c0031t0002g0030 | 3 | HG00438.hp2 HG03927.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7318-266A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132288 | ||||||
chr12:120132305 | CTG | C | 69 | a0001c0002t0001g0035a0001c0002t0001g0130a0001c0002t0002g0002others(66): Show | 73 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.7318-285_7318-284d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132305 | ||||||
chr12:120132400 | G | A | 1 | a0001c0002t0002g0294 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.7318-378C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132400 | ||||||
chr12:120132446 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7318-424G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132446 | ||||||
chr12:120132541 | C | A | 1 | a0002c0008t0002g0194 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.7318-519G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132541 | ||||||
chr12:120132616 | A | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.7318-594T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132616 | ||||||
chr12:120132663 | G | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7318-641C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132663 | ||||||
chr12:120132696 | G | A | 1 | a0001c0020t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7318-674C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132696 | ||||||
chr12:120132898 | C | A | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.7318-876G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120132898 | ||||||
chr12:120133004 | T | G | 1 | a0001c0004t0003g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7318-982A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133004 | ||||||
chr12:120133118 | C | T | 2 | a0001c0002t0002g0161a0001c0031t0002g0030 | 2 | NA19080.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7318-1096G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133118 | ||||||
chr12:120133165 | G | T | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.7317+1126C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133165 | ||||||
chr12:120133223 | C | T | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.7317+1068G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133223 | ||||||
chr12:120133229 | C | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 149 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.7317+1062G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133229 | ||||||
chr12:120133234 | A | G | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7317+1057T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133234 | ||||||
chr12:120133255 | C | T | 2 | a0006c0033t0004g0107a0013c0024t0001g0297 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.7317+1036G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133255 | ||||||
chr12:120133280 | A | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 92 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.7317+1011T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133280 | ||||||
chr12:120133546 | C | T | 1 | a0001c0002t0002g0177 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.7317+745G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133546 | ||||||
chr12:120133810 | T | C | 24 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0049others(21): Show | 26 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.7317+481A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120133810 | ||||||
chr12:120134072 | A | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.7317+219T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120134072 | ||||||
chr12:120134142 | T | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7317+149A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120134142 | ||||||
chr12:120134175 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.7317+116C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 53/57 | chr12 | 120134175 | ||||||
chr12:120134467 | G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0269 | 2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.7203-62C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 52/57 | chr12 | 120134467 | ||||||
chr12:120134471 | G | C | 1 | a0001c0002t0002g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.7202+62C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 52/57 | chr12 | 120134471 | ||||||
chr12:120134526 | G | A | 1 | a0001c0002t0001g0043 | 1 | HG03579.hp2 | splice_region_variant&intron_variant | LOW | c.7202+7C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 52/57 | chr12 | 120134526 | ||||||
chr12:120134794 | A | C | 5 | a0001c0005t0001g0092a0001c0005t0001g0093a0001c0014t0001g0079others(2): Show | 5 | HG00438.hp2 HG01891.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.7009-68T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120134794 | ||||||
chr12:120134818 | C | G | 1 | a0001c0004t0003g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7009-92G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120134818 | ||||||
chr12:120134921 | T | A | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7009-195A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120134921 | ||||||
chr12:120134982 | G | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0001g0210others(21): Show | 25 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.7009-256C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120134982 | ||||||
chr12:120134987 | G | A | 1 | a0001c0002t0002g0164 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.7009-261C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120134987 | ||||||
chr12:120135067 | T | G | 1 | a0001c0002t0002g0127 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.7009-341A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135067 | ||||||
chr12:120135184 | G | T | 4 | a0001c0011t0001g0231a0001c0011t0001g0247a0001c0011t0001g0248others(1): Show | 4 | HG01099.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.7009-458C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135184 | ||||||
chr12:120135320 | T | C | 1 | a0001c0004t0003g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7009-594A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135320 | ||||||
chr12:120135322 | C | T | 1 | a0001c0002t0002g0005 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7009-596G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135322 | ||||||
chr12:120135389 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.7009-663T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135389 | ||||||
chr12:120135525 | G | A | 1 | a0001c0003t0002g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.7009-799C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135525 | ||||||
chr12:120135607 | C | T | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7009-881G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135607 | ||||||
chr12:120135752 | A | C | 3 | a0004c0013t0001g0098a0004c0013t0001g0103a0004c0013t0001g0104 | 3 | HG02630.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.7008+750T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135752 | ||||||
chr12:120135907 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7008+595A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135907 | ||||||
chr12:120135962 | GC | G | 18 | a0001c0005t0002g0036a0001c0005t0002g0038a0001c0005t0002g0039others(15): Show | 18 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.7008+539delG | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120135962 | ||||||
chr12:120136011 | T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.7008+491A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120136011 | ||||||
chr12:120136289 | T | C | 1 | a0001c0035t0002g0124 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.7008+213A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120136289 | ||||||
chr12:120136394 | C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.7008+108G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 51/57 | chr12 | 120136394 | ||||||
chr12:120136846 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6778-114A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/57 | chr12 | 120136846 | ||||||
chr12:120136848 | G | C | 1 | a0001c0002t0002g0177 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.6778-116C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/57 | chr12 | 120136848 | ||||||
chr12:120136886 | T | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.6778-154A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/57 | chr12 | 120136886 | ||||||
chr12:120136910 | G | T | 2 | a0001c0012t0001g0221a0001c0012t0001g0282 | 2 | NA18948.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.6778-178C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/57 | chr12 | 120136910 | ||||||
chr12:120136978 | C | T | 1 | a0001c0009t0002g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6777+228G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/57 | chr12 | 120136978 | ||||||
chr12:120137148 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6777+58C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/57 | chr12 | 120137148 | ||||||
chr12:120137172 | C | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0209others(25): Show | 29 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.6777+34G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 50/57 | chr12 | 120137172 | ||||||
chr12:120137436 | C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.6663+109G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 49/57 | chr12 | 120137436 | ||||||
chr12:120137453 | A | G | 1 | a0001c0002t0002g0111 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.6663+92T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 49/57 | chr12 | 120137453 | ||||||
chr12:120137511 | C | A | 1 | a0001c0001t0001g0254 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.6663+34G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 49/57 | chr12 | 120137511 | ||||||
chr12:120137829 | G | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6394-15C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 48/57 | chr12 | 120137829 | ||||||
chr12:120138094 | G | C | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6250-50C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 47/57 | chr12 | 120138094 | ||||||
chr12:120138179 | A | G | 1 | a0001c0002t0002g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6250-135T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 47/57 | chr12 | 120138179 | ||||||
chr12:120138423 | G | C | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.6157-8C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 46/57 | chr12 | 120138423 | ||||||
chr12:120138435 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.6157-20G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 46/57 | chr12 | 120138435 | ||||||
chr12:120138461 | T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.6157-46A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 46/57 | chr12 | 120138461 | ||||||
chr12:120138469 | C | A | 1 | a0005c0015t0002g0143 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.6157-54G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 46/57 | chr12 | 120138469 | ||||||
chr12:120138580 | T | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.6156+115A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 46/57 | chr12 | 120138580 | ||||||
chr12:120138624 | G | A | 2 | a0001c0002t0002g0049a0001c0002t0002g0076 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6156+71C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 46/57 | chr12 | 120138624 | ||||||
chr12:120138967 | C | T | 6 | a0001c0003t0001g0034a0001c0003t0001g0037a0001c0003t0001g0040others(3): Show | 6 | HG01346.hp2 HG01928.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.5995-111G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120138967 | ||||||
chr12:120139009 | T | TA | 53 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(50): Show | 57 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.5995-154dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139009 | ||||||
chr12:120139023 | G | C | 1 | a0001c0002t0002g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5995-167C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139023 | ||||||
chr12:120139088 | T | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5995-232A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139088 | ||||||
chr12:120139268 | C | A | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5995-412G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139268 | ||||||
chr12:120139321 | T | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0280 | 3 | NA18941.hp1 NA18952.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.5995-465A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139321 | ||||||
chr12:120139322 | A | T | 1 | a0001c0002t0002g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5995-466T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139322 | ||||||
chr12:120139351 | G | A | 3 | a0001c0014t0001g0079a0001c0014t0001g0080a0001c0031t0002g0030 | 3 | HG01891.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5995-495C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139351 | ||||||
chr12:120139582 | C | T | 1 | a0001c0030t0001g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5995-726G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139582 | ||||||
chr12:120139999 | C | A | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5994+860G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120139999 | ||||||
chr12:120140038 | A | G | 1 | a0001c0002t0002g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5994+821T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140038 | ||||||
chr12:120140226 | T | C | 1 | a0001c0002t0002g0172 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5994+633A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140226 | ||||||
chr12:120140266 | A | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 116 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.5994+593T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140266 | ||||||
chr12:120140335 | T | C | 3 | a0001c0014t0001g0079a0001c0014t0001g0080a0001c0031t0002g0030 | 3 | HG01891.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5994+524A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140335 | ||||||
chr12:120140395 | T | C | 29 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(26): Show | 29 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.5994+464A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140395 | ||||||
chr12:120140504 | C | A | 1 | a0001c0020t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5994+355G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140504 | ||||||
chr12:120140585 | C | G | 1 | a0001c0002t0002g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.5994+274G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140585 | ||||||
chr12:120140689 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5994+170C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140689 | ||||||
chr12:120140777 | A | G | 29 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0095others(26): Show | 31 | HG00438.hp2 HG00597.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.5994+82T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 45/57 | chr12 | 120140777 | ||||||
chr12:120141118 | C | T | 1 | a0001c0002t0002g0144 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5830-95G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141118 | ||||||
chr12:120141362 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5830-339C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141362 | ||||||
chr12:120141375 | C | A | 1 | a0001c0002t0002g0112 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5830-352G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141375 | ||||||
chr12:120141465 | G | C | 12 | a0001c0006t0002g0017a0001c0006t0002g0019a0001c0006t0002g0020others(9): Show | 12 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.5830-442C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141465 | ||||||
chr12:120141596 | C | T | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.5830-573G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141596 | ||||||
chr12:120141623 | CT | C | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.5830-601delA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141623 | ||||||
chr12:120141644 | C | A | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5830-621G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141644 | ||||||
chr12:120141746 | G | A | 1 | a0001c0002t0002g0065 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5830-723C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141746 | ||||||
chr12:120141865 | T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.5829+642A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141865 | ||||||
chr12:120141910 | T | C | 1 | a0001c0007t0002g0141 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5829+597A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141910 | ||||||
chr12:120141962 | T | C | 1 | a0001c0022t0001g0268 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5829+545A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141962 | ||||||
chr12:120141970 | C | T | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.5829+537G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120141970 | ||||||
chr12:120142122 | C | G | 2 | a0006c0033t0004g0107a0013c0024t0001g0297 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.5829+385G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120142122 | ||||||
chr12:120142153 | C | T | 1 | a0001c0002t0002g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5829+354G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120142153 | ||||||
chr12:120142459 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5829+48T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 44/57 | chr12 | 120142459 | ||||||
chr12:120142783 | C | CA | 4 | a0001c0006t0002g0017a0001c0006t0002g0019a0001c0006t0002g0022others(1): Show | 4 | HG01943.hp2 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.5613+40dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 43/57 | chr12 | 120142783 | ||||||
chr12:120142802 | G | A | 2 | a0001c0002t0002g0069a0001c0002t0002g0073 | 2 | HG01433.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.5613+22C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 43/57 | chr12 | 120142802 | ||||||
chr12:120143117 | T | C | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5496-176A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143117 | ||||||
chr12:120143249 | G | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5496-308C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143249 | ||||||
chr12:120143412 | G | A | 1 | a0001c0002t0002g0111 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.5496-471C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143412 | ||||||
chr12:120143523 | G | A | 2 | a0006c0033t0004g0107a0013c0024t0001g0297 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.5496-582C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143523 | ||||||
chr12:120143540 | C | G | 1 | a0001c0002t0001g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5496-599G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143540 | ||||||
chr12:120143571 | G | A | 1 | a0001c0022t0001g0268 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5496-630C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143571 | ||||||
chr12:120143587 | G | GA | 100 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.5496-647_5496-646i others(3): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143587 | ||||||
chr12:120143587 | G | GAA | 19 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0209others(16): Show | 20 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.5496-647_5496-646i others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143587 | ||||||
chr12:120143588 | G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(154): Show | 165 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.5496-647C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143588 | ||||||
chr12:120143814 | G | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5495+492C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143814 | ||||||
chr12:120143969 | A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.5495+337T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120143969 | ||||||
chr12:120144054 | G | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5495+252C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120144054 | ||||||
chr12:120144119 | G | A | 1 | a0001c0004t0003g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5495+187C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120144119 | ||||||
chr12:120144168 | G | A | 2 | a0001c0004t0003g0031a0015c0032t0001g0113 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.5495+138C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120144168 | ||||||
chr12:120144286 | C | T | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG02040.hp1 HG02056.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.5495+20G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 42/57 | chr12 | 120144286 | ||||||
chr12:120144623 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5352+16T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 41/57 | chr12 | 120144623 | ||||||
chr12:120145074 | C | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.5017-13G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 39/57 | chr12 | 120145074 | ||||||
chr12:120145665 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4948-335T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120145665 | ||||||
chr12:120146136 | G | A | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4948-806C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146136 | ||||||
chr12:120146265 | C | CA | 8 | a0001c0001t0001g0244a0001c0011t0001g0231a0001c0011t0001g0248others(5): Show | 8 | HG01099.hp1 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.4947+786dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146265 | ||||||
chr12:120146265 | CA | C | 11 | a0001c0001t0001g0029a0001c0001t0001g0101a0001c0001t0001g0215others(8): Show | 11 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.4947+786delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146265 | ||||||
chr12:120146368 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4947+684A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146368 | ||||||
chr12:120146486 | A | G | 1 | a0003c0010t0002g0178 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4947+566T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146486 | ||||||
chr12:120146587 | AT | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 150 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.4947+464delA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146587 | ||||||
chr12:120146756 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4947+296C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146756 | ||||||
chr12:120146883 | T | A | 1 | a0001c0020t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4947+169A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146883 | ||||||
chr12:120146883 | T | C | 1 | a0001c0004t0003g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4947+169A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146883 | ||||||
chr12:120146956 | A | G | 1 | a0005c0015t0002g0180 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4947+96T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120146956 | ||||||
chr12:120147046 | C | T | 1 | a0001c0002t0002g0122 | 1 | HG02738.hp2 | splice_region_variant&intron_variant | LOW | c.4947+6G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 38/57 | chr12 | 120147046 | ||||||
chr12:120147369 | G | A | 2 | a0001c0018t0001g0032a0001c0030t0001g0033 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4727-97C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 37/57 | chr12 | 120147369 | ||||||
chr12:120147432 | A | G | 5 | a0001c0001t0001g0213a0001c0001t0001g0232a0001c0001t0001g0234others(2): Show | 5 | HG00642.hp2 HG01168.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.4727-160T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 37/57 | chr12 | 120147432 | ||||||
chr12:120147480 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4727-208G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 37/57 | chr12 | 120147480 | ||||||
chr12:120147503 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4727-231C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 37/57 | chr12 | 120147503 | ||||||
chr12:120148156 | G | C | 1 | a0001c0002t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4726+11C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 37/57 | chr12 | 120148156 | ||||||
chr12:120148389 | A | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.4547-43T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120148389 | ||||||
chr12:120148589 | G | T | 1 | a0001c0002t0002g0198 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4547-243C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120148589 | ||||||
chr12:120148663 | A | T | 4 | a0001c0006t0002g0017a0001c0006t0002g0019a0001c0006t0002g0022others(1): Show | 4 | HG01943.hp2 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4547-317T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120148663 | ||||||
chr12:120148986 | A | AT | 21 | a0001c0001t0001g0108a0001c0001t0001g0214a0001c0001t0001g0219others(18): Show | 21 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.4546+619dupA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120148986 | ||||||
chr12:120149001 | G | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(275): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.4546+605C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120149001 | ||||||
chr12:120149097 | T | TG | 117 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.4546+508dupC | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120149097 | ||||||
chr12:120149106 | A | G | 4 | a0001c0001t0001g0208a0001c0001t0001g0283a0001c0004t0003g0031others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4546+500T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120149106 | ||||||
chr12:120149246 | G | T | 1 | a0001c0002t0002g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4546+360C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120149246 | ||||||
chr12:120149386 | G | A | 12 | a0001c0006t0002g0017a0001c0006t0002g0019a0001c0006t0002g0020others(9): Show | 12 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.4546+220C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120149386 | ||||||
chr12:120149395 | T | C | 1 | a0001c0020t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4546+211A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120149395 | ||||||
chr12:120149421 | C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 89 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.4546+185G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120149421 | ||||||
chr12:120149422 | A | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 91 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.4546+184T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 36/57 | chr12 | 120149422 | ||||||
chr12:120149729 | G | A | 3 | a0001c0014t0001g0079a0001c0014t0001g0080a0001c0031t0002g0030 | 3 | HG01891.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4432-9C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 35/57 | chr12 | 120149729 | ||||||
chr12:120149747 | G | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4432-27C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 35/57 | chr12 | 120149747 | ||||||
chr12:120149786 | G | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4432-66C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 35/57 | chr12 | 120149786 | ||||||
chr12:120149903 | G | A | 2 | a0001c0005t0002g0057a0001c0005t0002g0060 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4431+19C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 35/57 | chr12 | 120149903 | ||||||
chr12:120150391 | T | C | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4310-348A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120150391 | ||||||
chr12:120150397 | C | T | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4310-354G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120150397 | ||||||
chr12:120150671 | T | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.4309+474A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120150671 | ||||||
chr12:120150675 | T | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.4309+470A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120150675 | ||||||
chr12:120150797 | C | T | 10 | a0001c0006t0002g0017a0001c0006t0002g0019a0001c0006t0002g0020others(7): Show | 10 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.4309+348G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120150797 | ||||||
chr12:120150862 | A | G | 4 | a0001c0014t0001g0079a0001c0014t0001g0080a0001c0031t0002g0030others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.4309+283T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120150862 | ||||||
chr12:120150869 | T | G | 3 | a0001c0014t0001g0079a0001c0014t0001g0080a0001c0031t0002g0030 | 3 | HG01891.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4309+276A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120150869 | ||||||
chr12:120150992 | G | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0216a0001c0030t0001g0033 | 4 | HG02451.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4309+153C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120150992 | ||||||
chr12:120151038 | C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(101): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.4309+107G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120151038 | ||||||
chr12:120151048 | A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(282): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.4309+97T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120151048 | ||||||
chr12:120151051 | G | A | 1 | a0001c0003t0001g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4309+94C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 34/57 | chr12 | 120151051 | ||||||
chr12:120151426 | C | T | 2 | a0001c0005t0002g0057a0001c0005t0002g0060 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4063-35G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120151426 | ||||||
chr12:120151487 | A | T | 1 | a0001c0003t0001g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4063-96T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120151487 | ||||||
chr12:120151521 | A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(134): Show | 144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.4063-130T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120151521 | ||||||
chr12:120151797 | A | G | 1 | a0001c0002t0002g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4063-406T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120151797 | ||||||
chr12:120151798 | T | C | 1 | a0002c0008t0002g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4063-407A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120151798 | ||||||
chr12:120151971 | A | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 127 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.4063-580T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120151971 | ||||||
chr12:120151990 | G | A | 3 | a0001c0005t0002g0036a0001c0005t0002g0038a0001c0005t0002g0039 | 3 | HG02486.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4063-599C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120151990 | ||||||
chr12:120152013 | GTAAAGTT others(3): Show |
G | 1 | a0001c0002t0002g0198 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4063-632_4063-623d others(12): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152013 | ||||||
chr12:120152017 | AGTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4063-636_4063-627d others(12): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152017 | ||||||
chr12:120152071 | C | G | 1 | a0001c0001t0001g0258 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4063-680G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152071 | ||||||
chr12:120152107 | A | G | 1 | a0001c0002t0002g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4063-716T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152107 | ||||||
chr12:120152249 | G | A | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.4063-858C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152249 | ||||||
chr12:120152280 | CAGCCTCC others(241): Show |
C | 1 | a0001c0014t0001g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4062+685_4063-890d others(2): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152280 | ||||||
chr12:120152385 | A | ACG | 31 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0001g0210others(28): Show | 32 | HG00408.hp2 HG02129.hp1 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.4062+826_4062+827d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152385 | ||||||
chr12:120152385 | A | G | 4 | a0001c0011t0001g0231a0001c0011t0001g0247a0001c0011t0001g0248others(1): Show | 4 | HG01099.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4062+828T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152385 | ||||||
chr12:120152387 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4062+826C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152387 | ||||||
chr12:120152387 | GCGCACAC others(239): Show |
G | 1 | a0001c0014t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4062+580_4062+825d others(2): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152387 | ||||||
chr12:120152389 | G | GCA | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.4062+822_4062+823d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152389 | ||||||
chr12:120152389 | G | GCACA | 24 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0099others(21): Show | 24 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.4062+820_4062+823d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152389 | ||||||
chr12:120152391 | ACACACAC others(239): Show |
A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4062+576_4062+821d others(2): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152391 | ||||||
chr12:120152415 | T | A | 1 | a0001c0002t0002g0117 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4062+798A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152415 | ||||||
chr12:120152421 | T | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.4062+792A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152421 | ||||||
chr12:120152429 | TATATATA others(239): Show |
T | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4062+538_4062+783d others(2): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152429 | ||||||
chr12:120152637 | GCACA | G | 5 | a0001c0002t0002g0182a0001c0009t0002g0016a0001c0009t0002g0024others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.4062+572_4062+575d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152637 | ||||||
chr12:120152639 | A | ACG | 21 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 22 | HG00408.hp2 HG01169.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.4062+573_4062+574i others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152639 | ||||||
chr12:120152639 | A | G | 1 | a0001c0014t0001g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4062+574T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152639 | ||||||
chr12:120152641 | A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(96): Show | 106 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.4062+572T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152641 | ||||||
chr12:120152669 | T | C | 1 | a0001c0020t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4062+544A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152669 | ||||||
chr12:120152831 | C | G | 3 | a0001c0014t0001g0079a0001c0014t0001g0080a0001c0031t0002g0030 | 3 | HG01891.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4062+382G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152831 | ||||||
chr12:120152891 | G | T | 1 | a0001c0002t0002g0166 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4062+322C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152891 | ||||||
chr12:120152960 | T | TA | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.4062+252dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120152960 | ||||||
chr12:120153029 | C | T | 24 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0049others(21): Show | 26 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.4062+184G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120153029 | ||||||
chr12:120153162 | G | A | 3 | a0001c0002t0002g0151a0001c0002t0002g0153a0001c0002t0002g0173 | 3 | HG02523.hp2 NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.4062+51C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120153162 | ||||||
chr12:120153175 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4062+38G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 33/57 | chr12 | 120153175 | ||||||
chr12:120153447 | C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(275): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.3868-40G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 32/57 | chr12 | 120153447 | ||||||
chr12:120154148 | T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.3702-239A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 31/57 | chr12 | 120154148 | ||||||
chr12:120154347 | T | A | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3702-438A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 31/57 | chr12 | 120154347 | ||||||
chr12:120154405 | G | C | 1 | a0001c0002t0002g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3702-496C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 31/57 | chr12 | 120154405 | ||||||
chr12:120154532 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3701+438G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 31/57 | chr12 | 120154532 | ||||||
chr12:120154636 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3701+334C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 31/57 | chr12 | 120154636 | ||||||
chr12:120154852 | A | G | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3701+118T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 31/57 | chr12 | 120154852 | ||||||
chr12:120155074 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3631-34C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 30/57 | chr12 | 120155074 | ||||||
chr12:120155141 | C | T | 1 | a0001c0002t0002g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3630+100G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 30/57 | chr12 | 120155141 | ||||||
chr12:120155511 | G | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3440+81C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 29/57 | chr12 | 120155511 | ||||||
chr12:120156330 | A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.3312+131T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 28/57 | chr12 | 120156330 | ||||||
chr12:120156387 | A | C | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3312+74T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 28/57 | chr12 | 120156387 | ||||||
chr12:120156400 | C | T | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3312+61G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 28/57 | chr12 | 120156400 | ||||||
chr12:120156430 | C | A | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3312+31G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 28/57 | chr12 | 120156430 | ||||||
chr12:120157005 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3088-13C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157005 | ||||||
chr12:120157217 | C | A | 2 | a0001c0002t0002g0090a0001c0002t0002g0091 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3088-225G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157217 | ||||||
chr12:120157319 | C | T | 1 | a0001c0002t0002g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3088-327G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157319 | ||||||
chr12:120157350 | G | C | 1 | a0001c0001t0001g0286 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3088-358C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157350 | ||||||
chr12:120157372 | G | C | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3088-380C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157372 | ||||||
chr12:120157487 | C | T | 1 | a0001c0002t0002g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3087+362G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157487 | ||||||
chr12:120157595 | C | T | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3087+254G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157595 | ||||||
chr12:120157670 | G | C | 1 | a0001c0002t0002g0127 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3087+179C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157670 | ||||||
chr12:120157782 | C | T | 1 | a0001c0020t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3087+67G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157782 | ||||||
chr12:120157789 | A | G | 1 | a0001c0002t0002g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3087+60T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157789 | ||||||
chr12:120157826 | G | A | 1 | a0001c0003t0001g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3087+23C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 26/57 | chr12 | 120157826 | ||||||
chr12:120158079 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2906-49C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 25/57 | chr12 | 120158079 | ||||||
chr12:120158266 | G | C | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2905+194C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 25/57 | chr12 | 120158266 | ||||||
chr12:120158797 | G | A | 2 | a0001c0002t0002g0187a0001c0002t0002g0189 | 2 | HG00099.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2750-182C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120158797 | ||||||
chr12:120158805 | G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.2750-190C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120158805 | ||||||
chr12:120158846 | A | G | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2750-231T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120158846 | ||||||
chr12:120158915 | A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.2750-300T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120158915 | ||||||
chr12:120158993 | C | G | 1 | a0001c0002t0002g0166 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2750-378G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120158993 | ||||||
chr12:120159374 | C | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG02071.hp1 NA18971.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2749+451G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120159374 | ||||||
chr12:120159466 | C | T | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2749+359G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120159466 | ||||||
chr12:120159601 | T | C | 1 | a0001c0002t0002g0004 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2749+224A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120159601 | ||||||
chr12:120159628 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2749+197C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120159628 | ||||||
chr12:120159681 | G | A | 2 | a0001c0005t0002g0057a0001c0005t0002g0060 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2749+144C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120159681 | ||||||
chr12:120159744 | ACAAGCAC others(18): Show |
A | 2 | a0001c0001t0001g0204a0001c0001t0001g0285 | 2 | HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2749+56_2749+80del others(25): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 24/57 | chr12 | 120159744 | ||||||
chr12:120160422 | A | G | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2437-167T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 22/57 | chr12 | 120160422 | ||||||
chr12:120160565 | A | C | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2437-310T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 22/57 | chr12 | 120160565 | ||||||
chr12:120160681 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2437-426C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 22/57 | chr12 | 120160681 | ||||||
chr12:120160973 | A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2436+517T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 22/57 | chr12 | 120160973 | ||||||
chr12:120161306 | A | G | 3 | a0001c0003t0001g0050a0001c0003t0001g0053a0001c0003t0002g0052 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2436+184T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 22/57 | chr12 | 120161306 | ||||||
chr12:120161370 | G | A | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2436+120C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 22/57 | chr12 | 120161370 | ||||||
chr12:120161480 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2436+10C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 22/57 | chr12 | 120161480 | ||||||
chr12:120161692 | C | G | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2343-109G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 21/57 | chr12 | 120161692 | ||||||
chr12:120161699 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2343-116C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 21/57 | chr12 | 120161699 | ||||||
chr12:120161847 | C | T | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2342+33G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 21/57 | chr12 | 120161847 | ||||||
chr12:120162121 | A | G | 1 | a0001c0003t0001g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2164-63T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 20/57 | chr12 | 120162121 | ||||||
chr12:120162198 | G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 127 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.2164-140C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 20/57 | chr12 | 120162198 | ||||||
chr12:120162368 | T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(155): Show | 166 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2164-310A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 20/57 | chr12 | 120162368 | ||||||
chr12:120162385 | C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0292 | 2 | NA18956.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.2164-327G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 20/57 | chr12 | 120162385 | ||||||
chr12:120162398 | T | C | 1 | a0003c0010t0002g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2164-340A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 20/57 | chr12 | 120162398 | ||||||
chr12:120162439 | G | T | 1 | a0001c0020t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2164-381C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 20/57 | chr12 | 120162439 | ||||||
chr12:120162761 | G | A | 2 | a0001c0018t0001g0032a0001c0030t0001g0033 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2163+86C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 20/57 | chr12 | 120162761 | ||||||
chr12:120163014 | C | A | 2 | a0001c0004t0003g0031a0015c0032t0001g0113 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2039-43G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 19/57 | chr12 | 120163014 | ||||||
chr12:120163024 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2038+46T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 19/57 | chr12 | 120163024 | ||||||
chr12:120163263 | T | C | 2 | a0001c0004t0003g0031a0015c0032t0001g0113 | 2 | HG02257.hp1 HG02965.hp1 |
splice_region_variant&intron_variant | LOW | c.1849-4A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120163263 | ||||||
chr12:120163321 | C | T | 1 | a0001c0002t0002g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1849-62G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120163321 | ||||||
chr12:120163641 | G | A | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1849-382C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120163641 | ||||||
chr12:120163717 | C | T | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1849-458G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120163717 | ||||||
chr12:120163792 | A | G | 1 | a0010c0026t0002g0062 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1849-533T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120163792 | ||||||
chr12:120163875 | C | A | 2 | a0001c0002t0002g0122a0001c0002t0002g0152 | 2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1848+461G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120163875 | ||||||
chr12:120163888 | C | T | 93 | a0001c0002t0001g0130a0001c0002t0001g0162a0001c0002t0002g0002others(90): Show | 97 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1848+448G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120163888 | ||||||
chr12:120163985 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1848+351G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120163985 | ||||||
chr12:120164040 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1848+296C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120164040 | ||||||
chr12:120164073 | C | T | 2 | a0001c0004t0003g0031a0015c0032t0001g0113 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1848+263G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120164073 | ||||||
chr12:120164147 | A | C | 3 | a0001c0003t0001g0050a0001c0003t0001g0053a0001c0003t0002g0052 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1848+189T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120164147 | ||||||
chr12:120164274 | T | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 145 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1848+62A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 18/57 | chr12 | 120164274 | ||||||
chr12:120164631 | G | A | 1 | a0001c0002t0001g0035 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1688+15C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 17/57 | chr12 | 120164631 | ||||||
chr12:120164778 | A | G | 6 | a0001c0006t0002g0020a0001c0009t0002g0016a0001c0009t0002g0024others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1613-57T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120164778 | ||||||
chr12:120164788 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1613-67G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120164788 | ||||||
chr12:120164865 | G | GT | 13 | a0001c0002t0002g0138a0001c0004t0001g0018a0001c0004t0001g0027others(10): Show | 13 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1613-145dupA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120164865 | ||||||
chr12:120164952 | CATATACA others(3): Show |
C | 2 | a0001c0001t0001g0095a0001c0001t0001g0108 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1613-241_1613-232d others(12): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120164952 | ||||||
chr12:120165000 | T | TAC | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0105others(1): Show | 4 | HG02055.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613-280_1613-279i others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165000 | ||||||
chr12:120165000 | T | TACAC | 5 | a0001c0001t0001g0215a0001c0031t0002g0030a0004c0013t0001g0098others(2): Show | 5 | HG00639.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613-280_1613-279i others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165000 | ||||||
chr12:120165000 | T | TACACACA others(3): Show |
3 | a0001c0001t0001g0266a0001c0001t0001g0278a0001c0020t0001g0096 | 3 | HG00099.hp2 HG02071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1613-280_1613-279i others(12): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165000 | ||||||
chr12:120165000 | TATAC | T | 4 | a0001c0002t0002g0059a0001c0002t0002g0156a0006c0033t0004g0107others(1): Show | 4 | HG01884.hp1 HG02602.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1613-283_1613-280d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165000 | ||||||
chr12:120165002 | T | C | 16 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(13): Show | 16 | HG00099.hp2 HG00639.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1613-281A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | T | TAC | 5 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0208others(2): Show | 6 | HG01106.hp2 HG01109.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1613-283_1613-282d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | T | TACAC | 9 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0001t0001g0245others(6): Show | 9 | HG00597.hp1 HG00642.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1613-285_1613-282d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | T | TACACAC | 36 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0094others(33): Show | 39 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1613-287_1613-282d others(8): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | T | TACACACA others(1): Show |
20 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0201others(17): Show | 22 | HG00621.hp2 HG01243.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1613-289_1613-282d others(10): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | T | TACACACA others(3): Show |
15 | a0001c0001t0001g0010a0001c0001t0001g0207a0001c0001t0001g0214others(12): Show | 16 | HG01099.hp1 HG01934.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.1613-291_1613-282d others(12): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | T | TACACACA others(5): Show |
3 | a0001c0001t0001g0235a0001c0001t0001g0293a0008c0021t0001g0276 | 3 | HG02004.hp1 HG03927.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1613-293_1613-282d others(14): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | T | TATACACA others(7): Show |
2 | a0001c0018t0001g0032a0001c0030t0001g0033 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1613-282_1613-281i others(16): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | TAC | T | 39 | a0001c0002t0001g0035a0001c0002t0001g0043a0001c0002t0002g0132others(36): Show | 40 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1613-283_1613-282d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165002 | TACAC | T | 101 | a0001c0002t0001g0130a0001c0002t0001g0162a0001c0002t0002g0002others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1613-285_1613-282d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165002 | ||||||
chr12:120165004 | C | T | 2 | a0001c0002t0002g0153a0001c0002t0002g0173 | 2 | NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1613-283G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165004 | ||||||
chr12:120165006 | C | T | 1 | a0001c0002t0002g0173 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1613-285G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165006 | ||||||
chr12:120165008 | C | T | 4 | a0001c0007t0002g0136a0001c0007t0002g0140a0001c0007t0002g0141others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1613-287G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165008 | ||||||
chr12:120165034 | C | T | 3 | a0001c0014t0001g0080a0006c0033t0004g0107a0013c0024t0001g0297 | 3 | HG01884.hp1 HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1613-313G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165034 | ||||||
chr12:120165034 | CACAT | C | 4 | a0001c0005t0002g0036a0001c0005t0002g0038a0001c0005t0002g0039others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1613-317_1613-314d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165034 | ||||||
chr12:120165036 | C | T | 5 | a0001c0002t0002g0146a0001c0014t0001g0080a0001c0016t0001g0015others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613-315G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165036 | ||||||
chr12:120165036 | CAT | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0095a0001c0001t0001g0209others(19): Show | 23 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1613-317_1613-316d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165036 | ||||||
chr12:120165038 | T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 117 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1613-317A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165038 | ||||||
chr12:120165040 | T | C | 43 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0099others(40): Show | 43 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1613-319A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165040 | ||||||
chr12:120165042 | T | C | 12 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1613-321A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165042 | ||||||
chr12:120165049 | A | T | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1613-328T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165049 | ||||||
chr12:120165051 | A | T | 28 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(25): Show | 29 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1613-330T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165051 | ||||||
chr12:120165051 | AT | A | 13 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(10): Show | 13 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1613-331delA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165051 | ||||||
chr12:120165053 | T | A | 1 | a0009c0027t0002g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1613-332A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165053 | ||||||
chr12:120165196 | G | A | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1613-475C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165196 | ||||||
chr12:120165206 | T | G | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1613-485A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165206 | ||||||
chr12:120165242 | A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1613-521T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165242 | ||||||
chr12:120165249 | A | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1613-528T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165249 | ||||||
chr12:120165251 | G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1613-530C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165251 | ||||||
chr12:120165281 | T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1613-560A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165281 | ||||||
chr12:120165421 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1613-700G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165421 | ||||||
chr12:120165459 | C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1613-738G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165459 | ||||||
chr12:120165508 | C | T | 2 | a0006c0033t0004g0107a0013c0024t0001g0297 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1613-787G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165508 | ||||||
chr12:120165627 | C | G | 1 | a0001c0002t0002g0172 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1613-906G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165627 | ||||||
chr12:120165662 | C | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1613-941G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165662 | ||||||
chr12:120165814 | C | T | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1613-1093G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165814 | ||||||
chr12:120165845 | A | G | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1613-1124T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165845 | ||||||
chr12:120165917 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1613-1196C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165917 | ||||||
chr12:120165948 | C | T | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1613-1227G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120165948 | ||||||
chr12:120166017 | C | A | 1 | a0001c0002t0002g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1613-1296G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166017 | ||||||
chr12:120166021 | C | T | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1613-1300G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166021 | ||||||
chr12:120166067 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1613-1346G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166067 | ||||||
chr12:120166084 | G | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1613-1363C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166084 | ||||||
chr12:120166185 | C | G | 4 | a0003c0010t0002g0123a0003c0010t0002g0137a0003c0010t0002g0157others(1): Show | 4 | NA18962.hp1 NA18966.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613-1464G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166185 | ||||||
chr12:120166366 | T | C | 1 | a0001c0012t0001g0282 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1613-1645A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166366 | ||||||
chr12:120166401 | C | CA | 33 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0206others(30): Show | 33 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1613-1681dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166401 | ||||||
chr12:120166401 | CA | C | 11 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0101others(8): Show | 11 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1613-1681delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166401 | ||||||
chr12:120166445 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1613-1724T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166445 | ||||||
chr12:120166629 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1612+1579C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166629 | ||||||
chr12:120166636 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1612+1572C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166636 | ||||||
chr12:120166666 | T | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1612+1542A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166666 | ||||||
chr12:120166703 | C | CA | 10 | a0001c0001t0001g0097a0001c0001t0001g0240a0001c0001t0001g0270others(7): Show | 10 | HG00735.hp2 HG01192.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1612+1504dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166703 | ||||||
chr12:120166703 | CA | C | 6 | a0001c0001t0001g0251a0001c0001t0001g0283a0001c0002t0002g0160others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1612+1504delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166703 | ||||||
chr12:120166742 | G | A | 1 | a0001c0003t0001g0046 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1612+1466C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166742 | ||||||
chr12:120166769 | T | C | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1612+1439A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166769 | ||||||
chr12:120166876 | T | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1612+1332A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166876 | ||||||
chr12:120166984 | C | A | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1612+1224G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120166984 | ||||||
chr12:120167329 | G | T | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1612+879C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120167329 | ||||||
chr12:120167339 | C | T | 1 | a0001c0002t0002g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1612+869G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120167339 | ||||||
chr12:120167352 | CA | C | 10 | a0001c0002t0002g0061a0001c0002t0002g0076a0001c0003t0001g0041others(7): Show | 10 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1612+855delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120167352 | ||||||
chr12:120167352 | CAA | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 124 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1612+854_1612+855d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120167352 | ||||||
chr12:120167420 | A | G | 5 | a0001c0002t0002g0172a0002c0008t0002g0006a0002c0008t0002g0193others(2): Show | 6 | HG00597.hp2 HG00609.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1612+788T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120167420 | ||||||
chr12:120167675 | C | T | 4 | a0001c0009t0002g0016a0001c0009t0002g0024a0001c0009t0002g0025others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1612+533G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120167675 | ||||||
chr12:120168070 | C | T | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1612+138G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 16/57 | chr12 | 120168070 | ||||||
chr12:120168359 | T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(276): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1520-59A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168359 | ||||||
chr12:120168369 | T | C | 1 | a0001c0002t0002g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1520-69A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168369 | ||||||
chr12:120168526 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1520-226G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168526 | ||||||
chr12:120168707 | G | C | 1 | a0001c0002t0002g0061 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1520-407C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168707 | ||||||
chr12:120168729 | C | A | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1520-429G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168729 | ||||||
chr12:120168788 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1520-488G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168788 | ||||||
chr12:120168793 | A | G | 1 | a0001c0002t0001g0162 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1520-493T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168793 | ||||||
chr12:120168800 | T | C | 1 | a0001c0035t0002g0124 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1520-500A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168800 | ||||||
chr12:120168915 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1520-615G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120168915 | ||||||
chr12:120169209 | G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1520-909C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169209 | ||||||
chr12:120169224 | T | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1520-924A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169224 | ||||||
chr12:120169225 | C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1520-925G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169225 | ||||||
chr12:120169233 | C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1520-933G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169233 | ||||||
chr12:120169248 | G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1519+921C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169248 | ||||||
chr12:120169266 | A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1519+903T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169266 | ||||||
chr12:120169269 | TCC | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 127 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1519+898_1519+899d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169269 | ||||||
chr12:120169271 | C | T | 20 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(17): Show | 20 | HG00438.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1519+898G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169271 | ||||||
chr12:120169276 | C | CA | 85 | a0001c0001t0001g0119a0001c0002t0001g0035a0001c0002t0001g0130others(82): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1519+892dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169276 | ||||||
chr12:120169276 | CA | C | 25 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0049others(22): Show | 27 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1519+892delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169276 | ||||||
chr12:120169276 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1519+875_1519+892d others(20): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169276 | ||||||
chr12:120169278 | A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1519+891T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169278 | ||||||
chr12:120169279 | AAAAAAAA others(10): Show |
A | 138 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1519+873_1519+889d others(19): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169279 | ||||||
chr12:120169284 | AAAAAAAA others(5): Show |
A | 3 | a0001c0002t0002g0116a0001c0002t0002g0170a0001c0002t0002g0176 | 3 | HG00544.hp1 HG00621.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1519+873_1519+884d others(14): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169284 | ||||||
chr12:120169295 | A | AAAAAAAA others(6): Show |
3 | a0001c0005t0002g0057a0001c0006t0002g0017a0001c0009t0002g0026 | 3 | HG02258.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1519+873_1519+874i others(15): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169295 | ||||||
chr12:120169295 | A | AAAAAAAA others(5): Show |
10 | a0001c0004t0003g0031a0001c0005t0002g0060a0001c0006t0002g0021others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1519+873_1519+874i others(14): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169295 | ||||||
chr12:120169295 | A | AAAAAAAA others(4): Show |
2 | a0001c0006t0002g0019a0001c0006t0002g0020 | 2 | HG01943.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1519+873_1519+874i others(13): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169295 | ||||||
chr12:120169296 | G | A | 16 | a0001c0002t0002g0171a0001c0004t0003g0031a0001c0005t0002g0057others(13): Show | 16 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1519+873C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169296 | ||||||
chr12:120169421 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1519+748A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169421 | ||||||
chr12:120169445 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1519+724G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169445 | ||||||
chr12:120169522 | T | G | 21 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 22 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1519+647A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169522 | ||||||
chr12:120169582 | C | T | 1 | a0001c0002t0002g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1519+587G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169582 | ||||||
chr12:120169606 | C | G | 3 | a0001c0005t0001g0092a0001c0005t0001g0093a0001c0031t0002g0030 | 3 | HG00438.hp2 HG03927.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1519+563G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169606 | ||||||
chr12:120169611 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1519+558G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169611 | ||||||
chr12:120169652 | C | T | 2 | a0001c0002t0002g0148a0001c0002t0002g0160 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1519+517G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169652 | ||||||
chr12:120169695 | G | A | 18 | a0001c0005t0002g0036a0001c0005t0002g0038a0001c0005t0002g0039others(15): Show | 18 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1519+474C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169695 | ||||||
chr12:120169748 | T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1519+421A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169748 | ||||||
chr12:120169830 | G | A | 1 | a0001c0022t0001g0268 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1519+339C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169830 | ||||||
chr12:120169835 | G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02451.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1519+334C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169835 | ||||||
chr12:120169868 | T | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1519+301A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169868 | ||||||
chr12:120169969 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1519+200T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 15/57 | chr12 | 120169969 | ||||||
chr12:120170652 | T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1367-331A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120170652 | ||||||
chr12:120170686 | T | C | 2 | a0006c0033t0004g0107a0013c0024t0001g0297 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1367-365A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120170686 | ||||||
chr12:120170865 | T | A | 18 | a0001c0005t0002g0036a0001c0005t0002g0038a0001c0005t0002g0039others(15): Show | 18 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1367-544A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120170865 | ||||||
chr12:120170934 | G | C | 1 | a0001c0005t0001g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1367-613C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120170934 | ||||||
chr12:120170989 | G | A | 1 | a0001c0014t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1367-668C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120170989 | ||||||
chr12:120171141 | C | CA | 121 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 129 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1367-821dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171141 | ||||||
chr12:120171141 | C | CAA | 9 | a0001c0001t0001g0105a0001c0001t0001g0204a0001c0001t0001g0219others(6): Show | 9 | HG00621.hp2 HG02074.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367-822_1367-821d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171141 | ||||||
chr12:120171178 | T | C | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1367-857A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171178 | ||||||
chr12:120171317 | A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0105 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1367-996T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171317 | ||||||
chr12:120171319 | T | G | 2 | a0001c0002t0002g0058a0001c0002t0002g0059 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1367-998A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171319 | ||||||
chr12:120171521 | T | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 178 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1367-1200A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171521 | ||||||
chr12:120171595 | GATA | G | 4 | a0001c0007t0002g0136a0001c0007t0002g0140a0001c0007t0002g0141others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367-1277_1367-127 others(7): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171595 | ||||||
chr12:120171648 | G | A | 2 | a0001c0002t0002g0148a0001c0002t0002g0160 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1367-1327C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171648 | ||||||
chr12:120171860 | T | C | 1 | a0001c0016t0001g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1367-1539A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171860 | ||||||
chr12:120171933 | C | T | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1367-1612G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120171933 | ||||||
chr12:120172012 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1366+1641G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172012 | ||||||
chr12:120172028 | T | C | 1 | a0001c0002t0001g0162 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1366+1625A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172028 | ||||||
chr12:120172143 | C | T | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1366+1510G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172143 | ||||||
chr12:120172236 | A | C | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1366+1417T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172236 | ||||||
chr12:120172247 | T | C | 1 | a0001c0003t0001g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1366+1406A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172247 | ||||||
chr12:120172281 | G | A | 2 | a0001c0012t0001g0221a0001c0012t0001g0282 | 2 | NA18948.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1366+1372C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172281 | ||||||
chr12:120172362 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1366+1291A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172362 | ||||||
chr12:120172476 | C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1366+1177G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172476 | ||||||
chr12:120172612 | C | T | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366+1041G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172612 | ||||||
chr12:120172801 | G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG02055.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1366+852C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172801 | ||||||
chr12:120172817 | T | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1366+836A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172817 | ||||||
chr12:120172908 | G | A | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1366+745C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120172908 | ||||||
chr12:120173008 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1366+645A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120173008 | ||||||
chr12:120173025 | A | G | 4 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0053others(1): Show | 4 | HG00639.hp2 HG00735.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+628T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120173025 | ||||||
chr12:120173057 | C | CT | 25 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0002t0002g0063others(22): Show | 25 | HG00438.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1366+595dupA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120173057 | ||||||
chr12:120173057 | CT | C | 6 | a0001c0001t0001g0213a0001c0002t0002g0055a0001c0002t0002g0126others(3): Show | 6 | HG01106.hp1 HG01168.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1366+595delA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120173057 | ||||||
chr12:120173075 | T | C | 1 | a0001c0003t0001g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1366+578A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120173075 | ||||||
chr12:120173523 | T | A | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1366+130A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 14/57 | chr12 | 120173523 | ||||||
chr12:120174530 | C | T | 1 | a0001c0002t0002g0177 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1094-361G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/57 | chr12 | 120174530 | ||||||
chr12:120174789 | C | CA | 26 | a0001c0001t0001g0014a0001c0001t0001g0211a0001c0001t0001g0218others(23): Show | 26 | HG00408.hp2 HG00642.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1093+372dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/57 | chr12 | 120174789 | ||||||
chr12:120174789 | CA | C | 11 | a0001c0002t0002g0118a0001c0003t0001g0051a0001c0004t0001g0018others(8): Show | 11 | HG00323.hp1 HG00639.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1093+372delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/57 | chr12 | 120174789 | ||||||
chr12:120174882 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1093+280A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/57 | chr12 | 120174882 | ||||||
chr12:120174896 | C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1093+266G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/57 | chr12 | 120174896 | ||||||
chr12:120175126 | CA | C | 20 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0208others(17): Show | 20 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1093+35delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/57 | chr12 | 120175126 | ||||||
chr12:120175126 | CAA | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(97): Show | 106 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1093+34_1093+35del others(2): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/57 | chr12 | 120175126 | ||||||
chr12:120175126 | CAAA | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0095others(9): Show | 14 | HG00099.hp2 HG00639.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1093+33_1093+35del others(3): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 12/57 | chr12 | 120175126 | ||||||
chr12:120175542 | A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 130 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1042+204T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 11/57 | chr12 | 120175542 | ||||||
chr12:120175574 | C | G | 1 | a0007c0019t0001g0239 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1042+172G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 11/57 | chr12 | 120175574 | ||||||
chr12:120175595 | C | A | 1 | a0001c0001t0001g0284 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1042+151G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 11/57 | chr12 | 120175595 | ||||||
chr12:120175625 | C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 146 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1042+121G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 11/57 | chr12 | 120175625 | ||||||
chr12:120175642 | TGCC | T | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1042+101_1042+103d others(5): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 11/57 | chr12 | 120175642 | ||||||
chr12:120175660 | A | T | 1 | a0001c0009t0002g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1042+86T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 11/57 | chr12 | 120175660 | ||||||
chr12:120175681 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1042+65G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 11/57 | chr12 | 120175681 | ||||||
chr12:120176290 | C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.839-73G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/57 | chr12 | 120176290 | ||||||
chr12:120176776 | C | CT | 12 | a0001c0006t0002g0017a0001c0006t0002g0019a0001c0006t0002g0020others(9): Show | 12 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.839-560dupA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/57 | chr12 | 120176776 | ||||||
chr12:120176844 | G | A | 18 | a0001c0005t0002g0036a0001c0005t0002g0038a0001c0005t0002g0039others(15): Show | 18 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.838+603C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/57 | chr12 | 120176844 | ||||||
chr12:120176920 | C | A | 1 | a0001c0002t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.838+527G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/57 | chr12 | 120176920 | ||||||
chr12:120177034 | G | A | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.838+413C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/57 | chr12 | 120177034 | ||||||
chr12:120177157 | G | A | 4 | a0001c0002t0002g0135a0001c0002t0002g0139a0001c0002t0002g0163others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+290C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/57 | chr12 | 120177157 | ||||||
chr12:120177356 | C | G | 1 | a0016c0034t0002g0147 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.838+91G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/57 | chr12 | 120177356 | ||||||
chr12:120177412 | T | A | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.838+35A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 9/57 | chr12 | 120177412 | ||||||
chr12:120177626 | T | C | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.729+58A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 8/57 | chr12 | 120177626 | ||||||
chr12:120177768 | C | T | 1 | a0001c0020t0001g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661-16G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 7/57 | chr12 | 120177768 | ||||||
chr12:120177897 | A | C | 1 | a0001c0002t0002g0146 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.661-145T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 7/57 | chr12 | 120177897 | ||||||
chr12:120177976 | G | C | 1 | a0001c0002t0001g0162 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.661-224C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 7/57 | chr12 | 120177976 | ||||||
chr12:120178003 | G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(47): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.661-251C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 7/57 | chr12 | 120178003 | ||||||
chr12:120178189 | G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.660+436C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 7/57 | chr12 | 120178189 | ||||||
chr12:120178381 | AATAAGTG others(5): Show |
A | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.660+232_660+243del others(12): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 7/57 | chr12 | 120178381 | ||||||
chr12:120178386 | G | A | 7 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG00408.hp2 NA18944.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+239C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 7/57 | chr12 | 120178386 | ||||||
chr12:120178995 | T | A | 2 | a0001c0002t0002g0139a0001c0002t0002g0163 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.427-45A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120178995 | ||||||
chr12:120179015 | T | C | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.427-65A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179015 | ||||||
chr12:120179092 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.427-142T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179092 | ||||||
chr12:120179118 | T | C | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.427-168A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179118 | ||||||
chr12:120179255 | G | A | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.427-305C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179255 | ||||||
chr12:120179263 | G | A | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.427-313C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179263 | ||||||
chr12:120179324 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.427-374C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179324 | ||||||
chr12:120179397 | A | AT | 37 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(34): Show | 37 | HG00609.hp1 HG00642.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.427-448dupA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179397 | ||||||
chr12:120179461 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.427-511C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179461 | ||||||
chr12:120179486 | G | A | 2 | a0001c0017t0002g0174a0012c0028t0002g0175 | 2 | HG01106.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.427-536C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179486 | ||||||
chr12:120179778 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.427-828A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120179778 | ||||||
chr12:120180047 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.427-1097G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180047 | ||||||
chr12:120180097 | G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.427-1147C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180097 | ||||||
chr12:120180219 | T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 129 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.427-1269A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180219 | ||||||
chr12:120180275 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.427-1325C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180275 | ||||||
chr12:120180277 | T | C | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.427-1327A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180277 | ||||||
chr12:120180305 | C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 129 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.427-1355G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180305 | ||||||
chr12:120180444 | G | C | 1 | a0001c0001t0001g0264 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.427-1494C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180444 | ||||||
chr12:120180446 | C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0108 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.427-1496G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180446 | ||||||
chr12:120180558 | T | C | 1 | a0001c0002t0002g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.427-1608A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180558 | ||||||
chr12:120180562 | G | A | 1 | a0001c0002t0002g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.427-1612C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180562 | ||||||
chr12:120180700 | T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 129 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.427-1750A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180700 | ||||||
chr12:120180717 | G | A | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.427-1767C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180717 | ||||||
chr12:120180782 | A | G | 1 | a0005c0015t0002g0143 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.427-1832T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180782 | ||||||
chr12:120180862 | C | T | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.427-1912G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180862 | ||||||
chr12:120180915 | G | A | 16 | a0001c0002t0002g0109a0001c0002t0002g0110a0001c0002t0002g0116others(13): Show | 16 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.427-1965C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180915 | ||||||
chr12:120180986 | C | T | 10 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0084others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.427-2036G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180986 | ||||||
chr12:120180991 | C | CA | 118 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.427-2042dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120180991 | ||||||
chr12:120181118 | G | C | 2 | a0001c0014t0001g0079a0001c0014t0001g0080 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.427-2168C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181118 | ||||||
chr12:120181135 | T | G | 1 | a0001c0004t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.427-2185A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181135 | ||||||
chr12:120181264 | G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0280 | 3 | NA18952.hp1 NA18966.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.426+2305C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181264 | ||||||
chr12:120181465 | C | CAAAAAA | 26 | a0001c0001t0001g0119a0001c0002t0002g0005a0001c0002t0002g0013others(23): Show | 27 | HG00323.hp2 HG00438.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.426+2098_426+2103d others(8): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181465 | ||||||
chr12:120181465 | C | CAAAAAAA | 85 | a0001c0002t0001g0130a0001c0002t0001g0162a0001c0002t0002g0002others(82): Show | 90 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.426+2097_426+2103d others(9): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181465 | ||||||
chr12:120181465 | C | CAAAAAAA others(1): Show |
19 | a0001c0002t0001g0035a0001c0002t0002g0118a0001c0002t0002g0120others(16): Show | 19 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.426+2096_426+2103d others(10): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181465 | ||||||
chr12:120181465 | C | CAAAAAAA others(2): Show |
29 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(26): Show | 29 | HG01109.hp2 HG01243.hp1 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.426+2095_426+2103d others(11): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181465 | ||||||
chr12:120181465 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0105a0001c0004t0001g0085a0001c0004t0001g0086others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.426+2094_426+2103d others(12): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181465 | ||||||
chr12:120181465 | C | CAAAAAAA others(4): Show |
2 | a0001c0002t0002g0177a0004c0013t0001g0104 | 2 | HG02630.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.426+2093_426+2103d others(13): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181465 | ||||||
chr12:120181465 | CAAAA | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 108 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.426+2100_426+2103d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181465 | ||||||
chr12:120181484 | A | G | 1 | a0001c0014t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.426+2085T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181484 | ||||||
chr12:120181611 | G | A | 1 | a0008c0021t0001g0276 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.426+1958C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181611 | ||||||
chr12:120181668 | C | T | 10 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0084others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.426+1901G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181668 | ||||||
chr12:120181835 | G | A | 1 | a0001c0002t0002g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.426+1734C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181835 | ||||||
chr12:120181839 | C | CA | 8 | a0001c0002t0002g0122a0001c0002t0002g0129a0001c0002t0002g0197others(5): Show | 8 | HG01891.hp1 HG02056.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.426+1729dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181839 | ||||||
chr12:120181839 | C | CAAA | 13 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(10): Show | 13 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.426+1727_426+1729d others(5): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181839 | ||||||
chr12:120181839 | CA | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.426+1729delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181839 | ||||||
chr12:120181839 | CAA | C | 7 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(4): Show | 7 | HG00099.hp2 HG00642.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+1728_426+1729d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181839 | ||||||
chr12:120181866 | G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 89 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.426+1703C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181866 | ||||||
chr12:120181888 | T | C | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.426+1681A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120181888 | ||||||
chr12:120182173 | C | A | 1 | a0001c0001t0001g0264 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.426+1396G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182173 | ||||||
chr12:120182173 | CAAAA | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0001g0210others(18): Show | 22 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.426+1392_426+1395d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182173 | ||||||
chr12:120182206 | A | T | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.426+1363T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182206 | ||||||
chr12:120182347 | T | C | 12 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0004t0001g0081others(9): Show | 12 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.426+1222A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182347 | ||||||
chr12:120182475 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.426+1094G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182475 | ||||||
chr12:120182636 | T | C | 1 | a0001c0002t0001g0130 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.426+933A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182636 | ||||||
chr12:120182934 | C | CA | 121 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 129 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.426+634dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182934 | ||||||
chr12:120182934 | C | CAA | 8 | a0001c0001t0001g0105a0001c0001t0001g0202a0001c0001t0001g0207others(5): Show | 8 | HG02071.hp1 HG02132.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.426+633_426+634dup others(2): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182934 | ||||||
chr12:120182934 | CA | C | 6 | a0001c0003t0001g0051a0001c0004t0001g0018a0001c0005t0002g0060others(3): Show | 6 | HG00639.hp2 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.426+634delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120182934 | ||||||
chr12:120183140 | T | C | 1 | a0005c0015t0002g0180 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.426+429A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120183140 | ||||||
chr12:120183207 | C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.426+362G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120183207 | ||||||
chr12:120183261 | C | T | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.426+308G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120183261 | ||||||
chr12:120183441 | C | G | 10 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0084others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.426+128G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 5/57 | chr12 | 120183441 | ||||||
chr12:120183699 | G | T | 1 | a0001c0002t0002g0111 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.318-22C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 4/57 | chr12 | 120183699 | ||||||
chr12:120183751 | C | T | 1 | a0001c0022t0001g0268 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.318-74G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 4/57 | chr12 | 120183751 | ||||||
chr12:120183829 | T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 10 | HG00408.hp2 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-152A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 4/57 | chr12 | 120183829 | ||||||
chr12:120183881 | G | A | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.318-204C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 4/57 | chr12 | 120183881 | ||||||
chr12:120183883 | C | A | 1 | a0001c0002t0002g0181 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.318-206G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 4/57 | chr12 | 120183883 | ||||||
chr12:120184016 | A | C | 1 | a0001c0003t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.317+96T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 4/57 | chr12 | 120184016 | ||||||
chr12:120184069 | G | C | 1 | a0001c0002t0002g0013 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.317+43C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 4/57 | chr12 | 120184069 | ||||||
chr12:120184513 | C | T | 12 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0084others(9): Show | 12 | HG00438.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.186-270G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 3/57 | chr12 | 120184513 | ||||||
chr12:120184571 | G | A | 3 | a0001c0002t0002g0182a0001c0002t0002g0183a0001c0002t0002g0186 | 3 | HG01192.hp2 HG02074.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.185+253C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 3/57 | chr12 | 120184571 | ||||||
chr12:120184806 | C | T | 1 | a0001c0002t0002g0135 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.185+18G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 3/57 | chr12 | 120184806 | ||||||
chr12:120184914 | G | A | 10 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0084others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-27C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120184914 | ||||||
chr12:120185082 | A | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 130 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.122-195T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185082 | ||||||
chr12:120185328 | A | G | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.122-441T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185328 | ||||||
chr12:120185458 | T | C | 1 | a0001c0007t0002g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.122-571A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185458 | ||||||
chr12:120185505 | A | G | 1 | a0001c0002t0002g0134 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.122-618T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185505 | ||||||
chr12:120185521 | A | G | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.122-634T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185521 | ||||||
chr12:120185534 | C | A | 2 | a0001c0012t0001g0221a0001c0012t0001g0282 | 2 | NA18948.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.122-647G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185534 | ||||||
chr12:120185644 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.122-757G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185644 | ||||||
chr12:120185700 | A | G | 1 | a0001c0002t0002g0131 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.122-813T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185700 | ||||||
chr12:120185757 | C | T | 1 | a0001c0002t0002g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.122-870G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185757 | ||||||
chr12:120185872 | T | C | 1 | a0001c0002t0002g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122-985A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185872 | ||||||
chr12:120185879 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.122-992C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185879 | ||||||
chr12:120185931 | T | C | 10 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-1044A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185931 | ||||||
chr12:120185959 | A | G | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122-1072T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120185959 | ||||||
chr12:120186071 | C | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.122-1184G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186071 | ||||||
chr12:120186243 | G | A | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1356C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186243 | ||||||
chr12:120186249 | G | T | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1362C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186249 | ||||||
chr12:120186282 | A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(211): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.122-1395T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186282 | ||||||
chr12:120186285 | G | T | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1398C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186285 | ||||||
chr12:120186286 | A | G | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1399T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186286 | ||||||
chr12:120186289 | C | G | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1402G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186289 | ||||||
chr12:120186290 | G | C | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1403C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186290 | ||||||
chr12:120186294 | G | C | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1407C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186294 | ||||||
chr12:120186305 | G | T | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1418C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186305 | ||||||
chr12:120186308 | G | C | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1421C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186308 | ||||||
chr12:120186309 | A | T | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1422T>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186309 | ||||||
chr12:120186310 | G | T | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1423C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186310 | ||||||
chr12:120186312 | T | A | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1425A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186312 | ||||||
chr12:120186313 | T | A | 1 | a0001c0004t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-1426A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186313 | ||||||
chr12:120186411 | C | T | 10 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0084others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-1524G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186411 | ||||||
chr12:120186500 | A | G | 1 | a0001c0012t0001g0224 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.122-1613T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186500 | ||||||
chr12:120186604 | A | G | 1 | a0001c0002t0002g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.122-1717T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186604 | ||||||
chr12:120186768 | G | A | 2 | a0001c0001t0001g0223a0014c0023t0001g0222 | 2 | HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.122-1881C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186768 | ||||||
chr12:120186848 | G | T | 1 | a0001c0002t0002g0004 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.122-1961C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186848 | ||||||
chr12:120186852 | T | A | 1 | a0001c0004t0003g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.122-1965A>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186852 | ||||||
chr12:120186993 | G | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.122-2106C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120186993 | ||||||
chr12:120187067 | C | T | 4 | a0001c0005t0002g0036a0001c0005t0002g0038a0001c0005t0002g0039others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-2180G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187067 | ||||||
chr12:120187207 | G | T | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122-2320C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187207 | ||||||
chr12:120187213 | C | CT | 9 | a0001c0001t0001g0208a0001c0001t0001g0225a0001c0002t0002g0109others(6): Show | 9 | HG00673.hp2 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-2327dupA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187213 | ||||||
chr12:120187274 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.122-2387C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187274 | ||||||
chr12:120187315 | C | T | 1 | a0001c0003t0001g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.122-2428G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187315 | ||||||
chr12:120187467 | C | T | 1 | a0001c0002t0002g0133 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.122-2580G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187467 | ||||||
chr12:120187506 | A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(212): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.122-2619T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187506 | ||||||
chr12:120187590 | T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 127 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.122-2703A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187590 | ||||||
chr12:120187591 | G | A | 1 | a0001c0022t0001g0268 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.122-2704C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187591 | ||||||
chr12:120187636 | A | G | 1 | a0001c0011t0001g0231 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.121+2662T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187636 | ||||||
chr12:120187709 | C | T | 95 | a0001c0001t0001g0295a0001c0002t0001g0035a0001c0002t0001g0130others(92): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.121+2589G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187709 | ||||||
chr12:120187735 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.121+2563G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187735 | ||||||
chr12:120187753 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.121+2545G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187753 | ||||||
chr12:120187754 | G | A | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.121+2544C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187754 | ||||||
chr12:120187859 | C | T | 2 | a0001c0002t0002g0058a0001c0002t0002g0059 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.121+2439G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187859 | ||||||
chr12:120187887 | G | GA | 32 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(29): Show | 32 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.121+2410dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187887 | ||||||
chr12:120187888 | A | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.121+2410T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187888 | ||||||
chr12:120187899 | A | C | 2 | a0001c0001t0001g0204a0001c0005t0002g0036 | 2 | HG03540.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.121+2399T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187899 | ||||||
chr12:120187901 | AC | A | 16 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0108others(13): Show | 16 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.121+2396delG | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187901 | ||||||
chr12:120187902 | C | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(102): Show | 113 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.121+2396G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187902 | ||||||
chr12:120187905 | A | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0283 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.121+2393T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187905 | ||||||
chr12:120187916 | T | G | 1 | a0006c0033t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.121+2382A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120187916 | ||||||
chr12:120188026 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.121+2272G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188026 | ||||||
chr12:120188140 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.121+2158T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188140 | ||||||
chr12:120188294 | C | T | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.121+2004G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188294 | ||||||
chr12:120188357 | C | G | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.121+1941G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188357 | ||||||
chr12:120188357 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.121+1941G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188357 | ||||||
chr12:120188371 | T | C | 2 | a0001c0031t0002g0030a0013c0024t0001g0297 | 2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.121+1927A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188371 | ||||||
chr12:120188440 | G | GA | 85 | a0001c0001t0001g0119a0001c0001t0001g0295a0001c0002t0001g0035others(82): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.121+1857dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188440 | ||||||
chr12:120188440 | G | GAA | 45 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0095others(42): Show | 47 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.121+1856_121+1857d others(4): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188440 | ||||||
chr12:120188440 | G | GAAA | 70 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(67): Show | 76 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.121+1855_121+1857d others(5): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188440 | ||||||
chr12:120188440 | G | GAAAA | 8 | a0001c0001t0001g0207a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 8 | HG00621.hp2 HG03927.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.121+1854_121+1857d others(6): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188440 | ||||||
chr12:120188440 | GA | G | 13 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0006t0002g0017others(10): Show | 13 | HG01943.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.121+1857delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188440 | ||||||
chr12:120188441 | A | G | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.121+1857T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188441 | ||||||
chr12:120188460 | C | A | 1 | a0001c0001t0001g0278 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.121+1838G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188460 | ||||||
chr12:120188513 | A | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | NA18945.hp1 NA18971.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.121+1785T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188513 | ||||||
chr12:120188570 | A | G | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.121+1728T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188570 | ||||||
chr12:120188590 | C | T | 97 | a0001c0001t0001g0119a0001c0001t0001g0295a0001c0002t0001g0035others(94): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.121+1708G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188590 | ||||||
chr12:120188759 | G | A | 3 | a0001c0002t0002g0187a0001c0002t0002g0188a0001c0002t0002g0189 | 3 | HG00099.hp1 HG02004.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.121+1539C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188759 | ||||||
chr12:120188774 | G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 123 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.121+1524C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188774 | ||||||
chr12:120188844 | G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 127 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.121+1454C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188844 | ||||||
chr12:120188848 | C | CA | 7 | a0001c0001t0001g0207a0001c0001t0001g0279a0001c0001t0001g0286others(4): Show | 7 | HG00438.hp2 HG00597.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.121+1449dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120188848 | ||||||
chr12:120189105 | T | G | 1 | a0001c0002t0002g0191 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.121+1193A>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189105 | ||||||
chr12:120189200 | G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0280 | 3 | NA18952.hp1 NA18966.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.121+1098C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189200 | ||||||
chr12:120189232 | T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(211): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.121+1066A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189232 | ||||||
chr12:120189317 | C | T | 1 | a0003c0010t0002g0123 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.121+981G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189317 | ||||||
chr12:120189370 | C | CT | 8 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0002t0002g0120others(5): Show | 8 | HG00438.hp2 HG00544.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.121+927dupA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189370 | ||||||
chr12:120189538 | CT | C | 94 | a0001c0001t0001g0295a0001c0002t0001g0130a0001c0002t0001g0162others(91): Show | 98 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.121+759delA | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189538 | ||||||
chr12:120189847 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.121+451G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189847 | ||||||
chr12:120189848 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121+450C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189848 | ||||||
chr12:120189915 | G | A | 10 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0084others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+383C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120189915 | ||||||
chr12:120190006 | A | C | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121+292T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120190006 | ||||||
chr12:120190140 | G | A | 1 | a0001c0012t0001g0282 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.121+158C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120190140 | ||||||
chr12:120190224 | C | CA | 31 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0058others(28): Show | 34 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.121+73dupT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120190224 | ||||||
chr12:120190224 | C | CAA | 6 | a0001c0002t0002g0196a0001c0005t0001g0092a0001c0005t0001g0093others(3): Show | 6 | HG00438.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+72_121+73dupTT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120190224 | ||||||
chr12:120190224 | CA | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 125 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.121+73delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120190224 | ||||||
chr12:120190238 | A | G | 1 | a0001c0031t0002g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121+60T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120190238 | ||||||
chr12:120190239 | A | G | 1 | a0001c0002t0002g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.121+59T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 2/57 | chr12 | 120190239 | ||||||
chr12:120190562 | G | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.19-162C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120190562 | ||||||
chr12:120190730 | T | C | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.19-330A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120190730 | ||||||
chr12:120190793 | C | A | 1 | a0001c0002t0002g0197 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.19-393G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120190793 | ||||||
chr12:120190839 | C | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.19-439G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120190839 | ||||||
chr12:120190896 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.19-496C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120190896 | ||||||
chr12:120190925 | G | A | 10 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0084others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.19-525C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120190925 | ||||||
chr12:120191114 | A | C | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG02040.hp1 HG02056.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-714T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120191114 | ||||||
chr12:120191184 | C | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(211): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.19-784G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120191184 | ||||||
chr12:120191375 | G | T | 1 | a0001c0002t0002g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.19-975C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120191375 | ||||||
chr12:120191411 | G | C | 1 | a0001c0002t0002g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.19-1011C>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120191411 | ||||||
chr12:120191458 | C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0108 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.19-1058G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120191458 | ||||||
chr12:120191599 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.19-1199A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120191599 | ||||||
chr12:120191680 | T | C | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.19-1280A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120191680 | ||||||
chr12:120192169 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19-1769A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192169 | ||||||
chr12:120192484 | T | C | 2 | a0001c0002t0002g0090a0001c0002t0002g0091 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.19-2084A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192484 | ||||||
chr12:120192520 | G | A | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.19-2120C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192520 | ||||||
chr12:120192524 | G | A | 1 | a0015c0032t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.19-2124C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192524 | ||||||
chr12:120192529 | C | A | 2 | a0001c0002t0002g0007a0001c0002t0002g0198 | 3 | HG00140.hp1 HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.19-2129G>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192529 | ||||||
chr12:120192683 | G | T | 2 | a0001c0018t0001g0032a0001c0030t0001g0033 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.18+1997C>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192683 | ||||||
chr12:120192732 | GA | G | 6 | a0001c0001t0001g0293a0001c0002t0002g0109a0001c0002t0002g0110others(3): Show | 6 | HG00642.hp1 HG00673.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+1947delT | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192732 | ||||||
chr12:120192732 | GAA | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.18+1946_18+1947del others(2): Show |
GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192732 | ||||||
chr12:120192814 | G | A | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.18+1866C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192814 | ||||||
chr12:120192997 | T | C | 2 | a0001c0005t0001g0092a0001c0005t0001g0093 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.18+1683A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120192997 | ||||||
chr12:120193030 | C | G | 1 | a0001c0004t0003g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.18+1650G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120193030 | ||||||
chr12:120193081 | G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(102): Show | 113 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.18+1599C>T | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120193081 | ||||||
chr12:120193126 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.18+1554T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120193126 | ||||||
chr12:120193202 | A | C | 2 | a0001c0031t0002g0030a0013c0024t0001g0297 | 2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.18+1478T>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120193202 | ||||||
chr12:120193366 | T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(212): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.18+1314A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120193366 | ||||||
chr12:120193408 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.18+1272G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120193408 | ||||||
chr12:120193595 | C | T | 14 | a0001c0004t0001g0018a0001c0004t0001g0027a0001c0006t0002g0017others(11): Show | 14 | HG01109.hp2 HG01943.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.18+1085G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120193595 | ||||||
chr12:120193962 | A | G | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.18+718T>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120193962 | ||||||
chr12:120194143 | T | C | 2 | a0001c0001t0001g0295a0001c0002t0002g0294 | 2 | NA18979.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.18+537A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120194143 | ||||||
chr12:120194286 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.18+394A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120194286 | ||||||
chr12:120194315 | T | C | 1 | a0013c0024t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.18+365A>G | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120194315 | ||||||
chr12:120194443 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.18+237G>A | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120194443 | ||||||
chr12:120194446 | C | G | 1 | a0001c0002t0002g0013 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18+234G>C | GCN1 | ENSG00000089154.11 | transcript | ENST00000300648.7 | protein_coding | 1/57 | chr12 | 120194446 |