geneid | 116255 |
---|---|
ensemblid | ENSG00000124003.13 |
hgncid | 18210 |
symbol | MOGAT1 |
name | monoacylglycerol O-acyltransferase 1 |
refseq_nuc | NM_058165.3 |
refseq_prot | NP_477513.2 |
ensembl_nuc | ENST00000446656.4 |
ensembl_prot | ENSP00000406674.3 |
mane_status | MANE Select |
chr | chr2 |
start | 222671658 |
end | 222709930 |
strand | + |
ver | v1.2 |
region | chr2:222671658-222709930 |
region5000 | chr2:222666658-222714930 |
regionname0 | MOGAT1_chr2_222671658_222709930 |
regionname5000 | MOGAT1_chr2_222666658_222714930 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 335 | 224 | 49 | 37 | 103 | 11 | 23 | 79 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0002 | 0/0 | 335 | 60 | 28 | 14 | 12 | 1 | 5 | 9 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0003 | 0/0 | 335 | 14 | 9 | 3 | 1 | 0 | 1 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0004 | 0/0 | 335 | 8 | 1 | 3 | 0 | 0 | 4 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0005 | 0/0 | 335 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0006 | 0/0 | 335 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0007 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0008 | 0/1 | 335 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0009 | 0/0 | 335 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0010 | 0/0 | 335 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0011 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1008 | 223 | 49 | 37 | 103 | 11 | 22 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0002 | 0/0 | 1008 | 60 | 28 | 14 | 12 | 1 | 5 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0003 | 0/0 | 1008 | 14 | 9 | 3 | 1 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0004 | 0/0 | 1008 | 8 | 1 | 3 | 0 | 0 | 4 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0005 | 0/0 | 1008 | 4 | 4 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0006 | 0/0 | 1008 | 3 | 2 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0007 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0008 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0009 | 0/1 | 1008 | 1 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0010 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0011 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
c0012 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 169 | 286 | 75 | 50 | 116 | 12 | 31 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
t0002 | 0/0 | 169 | 30 | 17 | 8 | 2 | 0 | 3 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
t0003 | 0/0 | 169 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
t0004 | 0/0 | 169 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0011 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1008 | 223 | 49 | 37 | 103 | 11 | 22 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0001c0011 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0002c0002 | 0/0 | 1008 | 60 | 28 | 14 | 12 | 1 | 5 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0003c0003 | 0/0 | 1008 | 14 | 9 | 3 | 1 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0004c0004 | 0/0 | 1008 | 8 | 1 | 3 | 0 | 0 | 4 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0005c0005 | 0/0 | 1008 | 4 | 4 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0006c0006 | 0/0 | 1008 | 3 | 2 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0007c0010 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0008c0009 | 0/1 | 1008 | 1 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0009c0008 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0010c0007 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0011c0012 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1176 | 204 | 38 | 34 | 101 | 11 | 19 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0001c0001t0002 | 0/0 | 1176 | 17 | 9 | 3 | 2 | 0 | 3 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0001c0001t0003 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0001c0001t0004 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0001c0011t0001 | 0/0 | 1176 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0002c0002t0001 | 0/0 | 1176 | 47 | 20 | 9 | 12 | 1 | 5 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0002c0002t0002 | 0/0 | 1176 | 13 | 8 | 5 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0003c0003t0001 | 0/0 | 1176 | 14 | 9 | 3 | 1 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0004c0004t0001 | 0/0 | 1176 | 8 | 1 | 3 | 0 | 0 | 4 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0005c0005t0001 | 0/0 | 1176 | 4 | 4 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0006c0006t0001 | 0/0 | 1176 | 3 | 2 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0007c0010t0001 | 0/0 | 1176 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0008c0009t0001 | 0/1 | 1176 | 1 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0009c0008t0001 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0010c0007t0001 | 0/0 | 1176 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
a0011c0012t0001 | 0/0 | 1176 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | copy fasta | chr2 | 222666658 | 222714930 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0011 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0001c0011t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0003c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0004c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0004c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0004c0004t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0004c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0004c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0004c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0004c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0005c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0005c0005t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0005c0005t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0005c0005t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0006c0006t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0006c0006t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0006c0006t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0007c0010t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0008c0009t0001g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0009c0008t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0010c0007t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
a0011c0012t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00639 | hp1 | a0003 | c0003 | t0001 | g0278 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00639 | hp2 | a0004 | c0004 | t0001 | g0176 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0031 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00735 | hp1 | a0006 | c0006 | t0001 | g0289 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01168 | hp1 | a0004 | c0004 | t0001 | g0241 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01169 | hp2 | a0004 | c0004 | t0001 | g0242 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0283 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0239 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01884 | hp2 | a0005 | c0005 | t0001 | g0271 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01891 | hp1 | a0004 | c0004 | t0001 | g0191 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01975 | hp1 | a0003 | c0003 | t0001 | g0288 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02040 | hp2 | a0011 | c0012 | t0001 | g0231 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CDX | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CDX | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02572 | hp1 | a0005 | c0005 | t0001 | g0275 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0267 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02683 | hp1 | a0004 | c0004 | t0001 | g0269 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02717 | hp1 | a0005 | c0005 | t0001 | g0276 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02723 | hp1 | a0009 | c0008 | t0001 | g0126 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0041 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02965 | hp2 | a0003 | c0003 | t0001 | g0286 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0256 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0209 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0290 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03130 | hp1 | a0003 | c0003 | t0001 | g0291 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0279 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03225 | hp1 | a0003 | c0003 | t0001 | g0284 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0272 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03453 | hp1 | a0003 | c0003 | t0001 | g0280 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03490 | hp1 | a0004 | c0004 | t0001 | g0120 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03492 | hp1 | a0004 | c0004 | t0001 | g0121 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03540 | hp1 | a0006 | c0006 | t0001 | g0285 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0261 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03704 | hp2 | a0004 | c0004 | t0001 | g0236 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03942 | hp1 | a0010 | c0007 | t0001 | g0237 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18957 | hp1 | a0007 | c0010 | t0001 | g0196 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0282 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19077 | hp1 | a0003 | c0003 | t0001 | g0277 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ASW | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA20905 | hp1 | a0001 | c0011 | t0001 | g0021 | SAS | GIH | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | GIH | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02109 | hp1 | a0005 | c0005 | t0001 | g0274 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG03471 | hp2 | a0003 | c0003 | t0001 | g0273 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | USA | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA20300 | hp1 | a0006 | c0006 | t0001 | g0281 | AFR | USA | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0287 | AFR | USA | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
homoSapiens_chm13v2 | hp1 | a0008 | c0009 | t0001 | g0244 | REF | REF | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0011 | REF | REF | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:222671822
|
G | A | 3 | a0003a0005a0006 | 21 | HG00639.hp1 HG00735.hp1 HG01361.hp1 others(18): Show |
missense_variant | MODERATE | c.37G>A | p.Ala13Thr | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/6 | 165/1176 | 37/1008 | 13/335 | chr2 | 222671822 | ||
chr2:222671864
|
A | C | 1 | a0011 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.79A>C | p.Lys27Gln | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/6 | 207/1176 | 79/1008 | 27/335 | chr2 | 222671864 | ||
chr2:222688467
|
G | T | 1 | a0007 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.218G>T | p.Ser73Ile | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/6 | 346/1176 | 218/1008 | 73/335 | chr2 | 222688467 | ||
chr2:222689344
|
C | A | 1 | a0010 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.353C>A | p.Ala118Asp | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/6 | 481/1176 | 353/1008 | 118/335 | chr2 | 222689344 | ||
chr2:222689415
|
G | C | 1 | a0004 | 8 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
missense_variant | MODERATE | c.424G>C | p.Val142Leu | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/6 | 552/1176 | 424/1008 | 142/335 | chr2 | 222689415 | ||
chr2:222694370
|
T | C | 4 | a0002a0006a0008others(1): Show | 65 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
missense_variant | MODERATE | c.487T>C | p.Ser163Pro | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/6 | 615/1176 | 487/1008 | 163/335 | chr2 | 222694370 | ||
chr2:222694392
|
C | A | 1 | a0009 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.509C>A | p.Ser170Tyr | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/6 | 637/1176 | 509/1008 | 170/335 | chr2 | 222694392 | ||
chr2:222694397
|
A | C | 1 | a0005 | 4 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(1): Show |
missense_variant | MODERATE | c.514A>C | p.Met172Leu | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/6 | 642/1176 | 514/1008 | 172/335 | chr2 | 222694397 | ||
chr2:222695090
|
G | A | 1 | a0008 | 1 | homoSapiens_chm13v2.hp1 | missense_variant&splice_region_variant | MODERATE | c.655G>A | p.Ala219Thr | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/6 | 783/1176 | 655/1008 | 219/335 | chr2 | 222695090 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:222688450
|
A | G | 1 | a0001c0011 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.201A>G | p.Arg67Arg | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/6 | 329/1176 | 201/1008 | 67/335 | chr2 | 222688450 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:222671709
|
G | A | 4 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(1): Show | 32 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/6 | 77 | chr2 | 222671709 | |||||
chr2:222709900
|
A | T | 1 | a0001c0001t0004 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 6/6 | 10 | chr2 | 222709900 | |||||
chr2:222709919
|
A | T | 1 | a0001c0001t0003 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*29A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 6/6 | 29 | chr2 | 222709919 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:222671953
|
C | T | 21 | a0003c0003t0001g0272a0003c0003t0001g0273a0003c0003t0001g0277others(18): Show | 21 | HG00639.hp1 HG00735.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+74C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222671953 | ||||||
chr2:222671958
|
T | C | 1 | a0001c0011t0001g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.94+79T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222671958 | ||||||
chr2:222672269
|
A | T | 1 | a0001c0001t0001g0270 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.94+390A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672269 | ||||||
chr2:222672379
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.94+500T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672379 | ||||||
chr2:222672526
|
T | C | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0050others(33): Show | 40 | HG00642.hp1 HG01109.hp2 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.94+647T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672526 | ||||||
chr2:222672556
|
C | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(216): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.94+677C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672556 | ||||||
chr2:222672563
|
T | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0002c0002t0001g0023others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+684T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672563 | ||||||
chr2:222672609
|
G | A | 30 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0002others(27): Show | 34 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.94+730G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672609 | ||||||
chr2:222672642
|
G | C | 30 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0002others(27): Show | 34 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.94+763G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672642 | ||||||
chr2:222672645
|
C | T | 30 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0002others(27): Show | 34 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.94+766C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672645 | ||||||
chr2:222672742
|
G | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(216): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.94+863G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672742 | ||||||
chr2:222672767
|
C | T | 1 | a0004c0004t0001g0269 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.94+888C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672767 | ||||||
chr2:222672856
|
A | C | 1 | a0002c0002t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.94+977A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672856 | ||||||
chr2:222672859
|
G | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(216): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.94+980G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672859 | ||||||
chr2:222672889
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.94+1010T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672889 | ||||||
chr2:222672889
|
T | TTTA | 20 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0113others(17): Show | 22 | HG00280.hp2 HG00621.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+1045_94+1047dup others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | |||||
chr2:222672889
|
T | TTTATTA | 64 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 69 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.94+1042_94+1047dup others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | |||||
chr2:222672889
|
T | TTTATTAT others(2): Show |
103 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0050others(100): Show | 111 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.94+1039_94+1047dup others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | |||||
chr2:222672889
|
T | TTTATTAT others(5): Show |
12 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+1036_94+1047dup others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | |||||
chr2:222672889
|
T | TTTTTTA | 3 | a0001c0001t0001g0025a0002c0002t0001g0024a0002c0002t0001g0256 | 3 | HG02280.hp1 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.94+1012_94+1013ins others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | |||||
chr2:222672889
|
T | TTTTTTAT others(5): Show |
9 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0257others(6): Show | 11 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+1012_94+1013ins others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | |||||
chr2:222672889
|
T | TTTTTTAT others(8): Show |
4 | a0001c0001t0001g0264a0002c0002t0001g0265a0002c0002t0001g0266others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1012_94+1013ins others(15): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | |||||
chr2:222672889
|
TTTA | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 59 | HG00597.hp2 HG00609.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.94+1045_94+1047del others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | |||||
chr2:222672958
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.94+1079C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672958 | ||||||
chr2:222672977
|
C | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(216): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.94+1098C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672977 | ||||||
chr2:222672982
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.94+1103C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672982 | ||||||
chr2:222673221
|
G | C | 23 | a0001c0001t0001g0139a0001c0001t0001g0179a0001c0001t0001g0180others(20): Show | 23 | HG00639.hp1 HG01361.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+1342G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673221 | ||||||
chr2:222673331
|
C | CAAAAA | 18 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0002others(15): Show | 22 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+1463_94+1467dup others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | |||||
chr2:222673331
|
C | CAAAAAA | 13 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0002g0028others(10): Show | 13 | HG00642.hp1 HG01243.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+1462_94+1467dup others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | |||||
chr2:222673331
|
C | CAAAAAAA | 18 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0136others(15): Show | 19 | HG00639.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+1461_94+1467dup others(7): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | |||||
chr2:222673331
|
C | CAAAAAAA others(1): Show |
109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(106): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+1460_94+1467dup others(8): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | |||||
chr2:222673331
|
C | CAAAAAAA others(2): Show |
32 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0129others(29): Show | 33 | HG01243.hp1 HG01361.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.94+1459_94+1467dup others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | |||||
chr2:222673331
|
C | CAAAAAAA others(3): Show |
7 | a0001c0001t0001g0264a0003c0003t0001g0278a0003c0003t0001g0279others(4): Show | 7 | HG00639.hp1 HG02145.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1458_94+1467dup others(10): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | |||||
chr2:222673331
|
C | CAAAAAAA others(4): Show |
18 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0181others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+1457_94+1467dup others(11): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | |||||
chr2:222673331
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0140a0003c0003t0001g0272 | 2 | HG01884.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.94+1456_94+1467dup others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | |||||
chr2:222673472
|
C | G | 14 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+1593C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673472 | ||||||
chr2:222673597
|
C | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(127): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.94+1718C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673597 | ||||||
chr2:222673656
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94+1777C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673656 | ||||||
chr2:222673673
|
C | G | 1 | a0003c0003t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.94+1794C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673673 | ||||||
chr2:222673676
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94+1797T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673676 | ||||||
chr2:222673703
|
A | T | 2 | a0002c0002t0001g0173a0010c0007t0001g0237 | 2 | HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.94+1824A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673703 | ||||||
chr2:222673714
|
G | C | 1 | a0003c0003t0001g0283 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.94+1835G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673714 | ||||||
chr2:222673819
|
T | G | 28 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0002others(25): Show | 32 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+1940T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673819 | ||||||
chr2:222673883
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.94+2004C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673883 | ||||||
chr2:222674156
|
C | T | 1 | a0001c0011t0001g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.94+2277C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674156 | ||||||
chr2:222674364
|
C | T | 4 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0052others(1): Show | 5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+2485C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674364 | ||||||
chr2:222674424
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0140others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+2545A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674424 | ||||||
chr2:222674460
|
T | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+2581T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674460 | ||||||
chr2:222674587
|
T | G | 1 | a0003c0003t0001g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.94+2708T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674587 | ||||||
chr2:222674646
|
G | A | 20 | a0003c0003t0001g0272a0003c0003t0001g0273a0003c0003t0001g0277others(17): Show | 20 | HG00639.hp1 HG01361.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.94+2767G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674646 | ||||||
chr2:222674880
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0129others(1): Show | 5 | HG01243.hp1 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+3001T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674880 | ||||||
chr2:222675229
|
A | C | 1 | a0001c0001t0003g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94+3350A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675229 | ||||||
chr2:222675240
|
A | T | 1 | a0003c0003t0001g0277 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.94+3361A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675240 | ||||||
chr2:222675310
|
G | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0257others(11): Show | 16 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+3431G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675310 | ||||||
chr2:222675353
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3474G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675353 | ||||||
chr2:222675481
|
C | CT | 124 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(121): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.94+3618dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222675481 | |||||
chr2:222675481
|
CT | C | 22 | a0001c0001t0001g0062a0001c0001t0001g0139a0001c0001t0001g0179others(19): Show | 22 | HG00639.hp1 HG01361.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+3618delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222675481 | |||||
chr2:222675487
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(5): Show | 9 | HG01496.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+3608T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675487 | ||||||
chr2:222675511
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.94+3632A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675511 | ||||||
chr2:222675580
|
T | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(176): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.94+3701T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675580 | ||||||
chr2:222675604
|
T | C | 30 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0002others(27): Show | 34 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.94+3725T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675604 | ||||||
chr2:222675629
|
A | G | 1 | a0004c0004t0001g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.94+3750A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675629 | ||||||
chr2:222675635
|
A | G | 1 | a0004c0004t0001g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.94+3756A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675635 | ||||||
chr2:222675654
|
T | C | 7 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0043others(4): Show | 8 | HG01257.hp1 HG02145.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+3775T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675654 | ||||||
chr2:222675693
|
A | T | 1 | a0002c0002t0001g0171 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.94+3814A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675693 | ||||||
chr2:222675920
|
C | T | 15 | a0001c0001t0001g0056a0001c0001t0001g0140a0001c0001t0001g0141others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.94+4041C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675920 | ||||||
chr2:222675955
|
A | T | 4 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0052others(1): Show | 5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+4076A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675955 | ||||||
chr2:222676080
|
G | A | 24 | a0001c0001t0001g0139a0001c0001t0001g0179a0001c0001t0001g0180others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.94+4201G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676080 | ||||||
chr2:222676122
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(5): Show | 9 | HG01496.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+4243C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676122 | ||||||
chr2:222676146
|
TCTC | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94+4270_94+4272del others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222676146 | |||||
chr2:222676150
|
C | CT | 23 | a0001c0001t0001g0172a0001c0001t0001g0234a0003c0003t0001g0272others(20): Show | 23 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.94+4286dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222676150 | |||||
chr2:222676158
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG02027.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.94+4279T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676158 | ||||||
chr2:222676166
|
A | T | 2 | a0002c0002t0001g0235a0002c0002t0001g0255 | 2 | NA18979.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.94+4287A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676166 | ||||||
chr2:222676175
|
C | T | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.94+4296C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676175 | ||||||
chr2:222676662
|
A | G | 2 | a0002c0002t0001g0235a0002c0002t0001g0255 | 2 | NA18979.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.94+4783A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676662 | ||||||
chr2:222676827
|
G | T | 1 | a0003c0003t0001g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.94+4948G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676827 | ||||||
chr2:222677351
|
T | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(192): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.94+5472T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222677351 | ||||||
chr2:222677397
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.94+5518G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222677397 | ||||||
chr2:222677512
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(139): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.94+5633A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222677512 | ||||||
chr2:222677996
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.94+6117C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222677996 | ||||||
chr2:222678024
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+6145C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678024 | ||||||
chr2:222678121
|
T | A | 1 | a0001c0001t0001g0192 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.94+6242T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678121 | ||||||
chr2:222678163
|
A | T | 35 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0002others(32): Show | 39 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.94+6284A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678163 | ||||||
chr2:222678177
|
A | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(138): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+6298A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678177 | ||||||
chr2:222678393
|
T | C | 1 | a0002c0002t0001g0256 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.94+6514T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678393 | ||||||
chr2:222678461
|
T | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0124others(14): Show | 19 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+6582T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678461 | ||||||
chr2:222678558
|
T | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94+6679T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678558 | ||||||
chr2:222678612
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94+6733T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678612 | ||||||
chr2:222678714
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.94+6835G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678714 | ||||||
chr2:222678757
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(139): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.94+6878A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678757 | ||||||
chr2:222678762
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.94+6883G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678762 | ||||||
chr2:222678766
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.94+6887C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678766 | ||||||
chr2:222678913
|
C | T | 14 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+7034C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678913 | ||||||
chr2:222678914
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(194): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.94+7035A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678914 | ||||||
chr2:222678985
|
T | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0181a0001c0001t0001g0183others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7106T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678985 | ||||||
chr2:222679107
|
A | G | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | NA18940.hp1 NA18950.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7228A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679107 | ||||||
chr2:222679377
|
C | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(138): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+7498C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679377 | ||||||
chr2:222679392
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(138): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+7513C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679392 | ||||||
chr2:222679393
|
A | G | 15 | a0001c0001t0001g0056a0001c0001t0001g0140a0001c0001t0001g0141others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.94+7514A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679393 | ||||||
chr2:222679532
|
C | T | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | NA18940.hp1 NA18950.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7653C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679532 | ||||||
chr2:222679818
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0150a0001c0001t0001g0198 | 5 | HG00099.hp2 HG00733.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7939G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679818 | ||||||
chr2:222679827
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.94+7948A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679827 | ||||||
chr2:222679897
|
T | A | 4 | a0001c0001t0002g0042a0002c0002t0001g0135a0002c0002t0001g0175others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+8018T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679897 | ||||||
chr2:222679945
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.94+8066A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679945 | ||||||
chr2:222680026
|
AG | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(8): Show | 12 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+8148delG | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680026 | ||||||
chr2:222680244
|
A | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(4): Show | 8 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-8100A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680244 | ||||||
chr2:222680264
|
G | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(147): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.95-8080G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680264 | ||||||
chr2:222680442
|
T | TAAAAGCA others(304): Show |
1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-7889_95-7888ins others(311): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222680442 | |||||
chr2:222680442
|
T | TAAAAGCA others(305): Show |
7 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(4): Show | 8 | HG01496.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-7889_95-7888ins others(312): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222680442 | |||||
chr2:222680445
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.95-7899A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680445 | ||||||
chr2:222680463
|
A | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(149): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.95-7881A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680463 | ||||||
chr2:222680625
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(57): Show | 65 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.95-7719C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680625 | ||||||
chr2:222680759
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-7585T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680759 | ||||||
chr2:222680817
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.95-7527T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680817 | ||||||
chr2:222681087
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-7257G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681087 | ||||||
chr2:222681134
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0001g0158others(8): Show | 13 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-7210C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681134 | ||||||
chr2:222681251
|
C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(56): Show | 64 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-7093C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681251 | ||||||
chr2:222681327
|
C | A | 4 | a0001c0001t0002g0042a0002c0002t0001g0135a0002c0002t0001g0175others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-7017C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681327 | ||||||
chr2:222681328
|
G | A | 59 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(56): Show | 64 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-7016G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681328 | ||||||
chr2:222681683
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.95-6661G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681683 | ||||||
chr2:222681744
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-6600G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681744 | ||||||
chr2:222682118
|
C | CCA | 3 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG02572.hp2 NA18952.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.95-6209_95-6208dup others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222682118 | |||||
chr2:222682118
|
CCA | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(128): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.95-6209_95-6208del others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222682118 | |||||
chr2:222682240
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0129others(3): Show | 7 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-6104C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682240 | ||||||
chr2:222682328
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-6016G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682328 | ||||||
chr2:222682366
|
C | G | 3 | a0003c0003t0001g0284a0003c0003t0001g0287a0003c0003t0001g0291 | 3 | HG03130.hp1 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.95-5978C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682366 | ||||||
chr2:222682371
|
A | G | 9 | a0001c0001t0001g0124a0001c0001t0001g0263a0002c0002t0001g0171others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-5973A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682371 | ||||||
chr2:222682418
|
C | T | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(145): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.95-5926C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682418 | ||||||
chr2:222682452
|
T | A | 9 | a0001c0001t0001g0124a0001c0001t0001g0263a0002c0002t0001g0171others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-5892T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682452 | ||||||
chr2:222682497
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.95-5847A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682497 | ||||||
chr2:222682545
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 12 | HG01496.hp2 HG01928.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-5799C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682545 | ||||||
chr2:222682637
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(112): Show | 123 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.95-5707G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682637 | ||||||
chr2:222682640
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(139): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.95-5704C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682640 | ||||||
chr2:222682690
|
C | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(129): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.95-5654C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682690 | ||||||
chr2:222682705
|
T | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(140): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.95-5639T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682705 | ||||||
chr2:222682713
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.95-5631C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682713 | ||||||
chr2:222682811
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0046a0001c0001t0002g0049 | 6 | HG02622.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-5533C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682811 | ||||||
chr2:222682984
|
G | A | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.95-5360G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682984 | ||||||
chr2:222682992
|
G | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(151): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.95-5352G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682992 | ||||||
chr2:222682993
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.95-5351C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682993 | ||||||
chr2:222683001
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(134): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.95-5343T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683001 | ||||||
chr2:222683134
|
G | A | 4 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0052others(1): Show | 5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-5210G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683134 | ||||||
chr2:222683182
|
T | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(61): Show | 69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-5162T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683182 | ||||||
chr2:222683205
|
G | GA | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(131): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.95-5125dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683205 | |||||
chr2:222683273
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(6): Show | 10 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-5071G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683273 | ||||||
chr2:222683430
|
T | TA | 7 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0129others(4): Show | 8 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-4900dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683430 | |||||
chr2:222683430
|
T | TAA | 57 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(54): Show | 62 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.95-4901_95-4900dup others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683430 | |||||
chr2:222683430
|
TA | T | 67 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(64): Show | 72 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.95-4900delA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683430 | |||||
chr2:222683430
|
TAA | T | 7 | a0001c0001t0001g0124a0001c0001t0001g0263a0003c0003t0001g0277others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-4901_95-4900del others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683430 | |||||
chr2:222683453
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.95-4891C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683453 | ||||||
chr2:222683465
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0137a0001c0001t0003g0054 | 4 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4879C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683465 | ||||||
chr2:222683556
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.95-4788C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683556 | ||||||
chr2:222683618
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.95-4726C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683618 | ||||||
chr2:222683758
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.95-4586C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683758 | ||||||
chr2:222684075
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-4269T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684075 | ||||||
chr2:222684299
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.95-4045G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684299 | ||||||
chr2:222684337
|
C | T | 7 | a0001c0001t0001g0124a0001c0001t0001g0263a0003c0003t0001g0277others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-4007C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684337 | ||||||
chr2:222684338
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(61): Show | 69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-4006G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684338 | ||||||
chr2:222684368
|
C | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(61): Show | 69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-3976C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684368 | ||||||
chr2:222684517
|
G | C | 3 | a0003c0003t0001g0284a0003c0003t0001g0287a0003c0003t0001g0291 | 3 | HG03130.hp1 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.95-3827G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684517 | ||||||
chr2:222684578
|
C | T | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(133): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-3766C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684578 | ||||||
chr2:222684586
|
T | C | 4 | a0001c0001t0001g0062a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG02165.hp1 NA18965.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3758T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684586 | ||||||
chr2:222684631
|
A | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(135): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.95-3713A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684631 | ||||||
chr2:222684733
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-3611C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684733 | ||||||
chr2:222684766
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(6): Show | 10 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-3578G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684766 | ||||||
chr2:222684855
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(61): Show | 69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-3489G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684855 | ||||||
chr2:222685064
|
T | C | 1 | a0002c0002t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.95-3280T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685064 | ||||||
chr2:222685153
|
G | T | 3 | a0002c0002t0001g0259a0002c0002t0001g0265a0002c0002t0001g0266 | 3 | HG02109.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.95-3191G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685153 | ||||||
chr2:222685293
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.95-3051C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685293 | ||||||
chr2:222685346
|
A | G | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(133): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-2998A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685346 | ||||||
chr2:222685410
|
T | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(133): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-2934T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685410 | ||||||
chr2:222685496
|
T | C | 3 | a0002c0002t0001g0259a0002c0002t0001g0265a0002c0002t0001g0266 | 3 | HG02109.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.95-2848T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685496 | ||||||
chr2:222685552
|
T | C | 1 | a0002c0002t0002g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.95-2792T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685552 | ||||||
chr2:222685556
|
C | T | 1 | a0002c0002t0001g0253 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.95-2788C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685556 | ||||||
chr2:222685598
|
C | CT | 61 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0051others(58): Show | 67 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-2726dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222685598 | |||||
chr2:222685598
|
CT | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0058others(21): Show | 26 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.95-2726delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222685598 | |||||
chr2:222685601
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.95-2743T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685601 | ||||||
chr2:222685602
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0137others(5): Show | 9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-2742T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685602 | ||||||
chr2:222685634
|
C | CTT | 4 | a0002c0002t0002g0044a0002c0002t0002g0045a0003c0003t0001g0288others(1): Show | 4 | HG01975.hp1 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-2709_95-2708dup others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222685634 | |||||
chr2:222685725
|
G | A | 49 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0055others(46): Show | 52 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.95-2619G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685725 | ||||||
chr2:222685729
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-2615T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685729 | ||||||
chr2:222685745
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0001g0158others(9): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-2599C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685745 | ||||||
chr2:222685746
|
A | G | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(133): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-2598A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685746 | ||||||
chr2:222685802
|
T | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0001g0158others(10): Show | 15 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-2542T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685802 | ||||||
chr2:222685881
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.95-2463C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685881 | ||||||
chr2:222685895
|
C | T | 1 | a0002c0002t0001g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.95-2449C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685895 | ||||||
chr2:222685961
|
C | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0192a0001c0001t0001g0210others(1): Show | 4 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2383C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685961 | ||||||
chr2:222686014
|
A | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0001g0158others(10): Show | 15 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-2330A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686014 | ||||||
chr2:222686057
|
T | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(6): Show | 10 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-2287T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686057 | ||||||
chr2:222686138
|
C | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(6): Show | 10 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-2206C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686138 | ||||||
chr2:222686266
|
C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(84): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-2078C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686266 | ||||||
chr2:222686320
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0248 | 2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.95-2024G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686320 | ||||||
chr2:222686428
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(61): Show | 69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-1916A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686428 | ||||||
chr2:222686451
|
A | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(5): Show | 9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-1893A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686451 | ||||||
chr2:222686497
|
C | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(86): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.95-1847C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686497 | ||||||
chr2:222686841
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.95-1503T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686841 | ||||||
chr2:222686851
|
A | G | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(133): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-1493A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686851 | ||||||
chr2:222686984
|
C | T | 1 | a0002c0002t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-1360C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686984 | ||||||
chr2:222687113
|
C | CA | 24 | a0001c0001t0001g0013a0001c0001t0001g0057a0001c0001t0001g0062others(21): Show | 25 | HG00642.hp2 HG00735.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-1205dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687113 | |||||
chr2:222687113
|
CA | C | 11 | a0001c0001t0001g0208a0002c0002t0001g0190a0003c0003t0001g0273others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-1205delA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687113 | |||||
chr2:222687113
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0117 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.95-1215_95-1205del others(11): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687113 | |||||
chr2:222687113
|
CAAAAAAA others(6): Show |
C | 4 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0052others(1): Show | 5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-1217_95-1205del others(13): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687113 | |||||
chr2:222687132
|
AAAAAAAA others(11): Show |
A | 28 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0056others(25): Show | 30 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-1208_95-1191del others(18): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687132 | |||||
chr2:222687133
|
AAAAAAAG others(10): Show |
A | 51 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0090others(48): Show | 54 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.95-1207_95-1191del others(17): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687133 | |||||
chr2:222687134
|
AAAAAAGA others(9): Show |
A | 52 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(49): Show | 57 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.95-1206_95-1191del others(16): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687134 | |||||
chr2:222687135
|
AAAAAGAA others(8): Show |
A | 5 | a0001c0001t0001g0096a0001c0001t0001g0159a0001c0001t0001g0170others(2): Show | 5 | HG01952.hp2 NA18995.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-1205_95-1191del others(15): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687135 | |||||
chr2:222687169
|
T | A | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(148): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.95-1175T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687169 | ||||||
chr2:222687341
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1003G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687341 | ||||||
chr2:222687374
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-970C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687374 | ||||||
chr2:222687633
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0001g0158others(9): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-711C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687633 | ||||||
chr2:222687705
|
C | T | 9 | a0003c0003t0001g0273a0003c0003t0001g0278a0003c0003t0001g0279others(6): Show | 9 | HG00639.hp1 HG03098.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-639C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687705 | ||||||
chr2:222687989
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0195 | 2 | HG01928.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-355G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687989 | ||||||
chr2:222688565
|
A | G | 52 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(49): Show | 56 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.273+43A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688565 | ||||||
chr2:222688615
|
G | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0129others(3): Show | 7 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+93G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688615 | ||||||
chr2:222688639
|
C | T | 1 | a0002c0002t0002g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.273+117C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688639 | ||||||
chr2:222688686
|
A | T | 52 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(49): Show | 56 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.273+164A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688686 | ||||||
chr2:222688704
|
T | C | 46 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0108others(43): Show | 49 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.273+182T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688704 | ||||||
chr2:222688806
|
A | G | 138 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 148 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.273+284A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688806 | ||||||
chr2:222688930
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.274-335A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688930 | ||||||
chr2:222689012
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0018others(61): Show | 69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.274-253G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222689012 | ||||||
chr2:222689020
|
G | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0178 | 2 | NA18982.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.274-245G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222689020 | ||||||
chr2:222689058
|
T | C | 4 | a0004c0004t0001g0120a0004c0004t0001g0121a0004c0004t0001g0191others(1): Show | 4 | HG01891.hp1 HG02683.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-207T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222689058 | ||||||
chr2:222689238
|
T | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(5): Show | 9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-27T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222689238 | ||||||
chr2:222689473
|
A | T | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.478+4A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689473 | ||||||
chr2:222689556
|
T | C | 52 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(49): Show | 56 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.478+87T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689556 | ||||||
chr2:222689624
|
C | T | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.478+155C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689624 | ||||||
chr2:222689625
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.478+156C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689625 | ||||||
chr2:222689626
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.478+157T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689626 | ||||||
chr2:222689706
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(5): Show | 9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.478+237G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689706 | ||||||
chr2:222689851
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.478+382G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689851 | ||||||
chr2:222689970
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.478+501C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689970 | ||||||
chr2:222690007
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.478+538C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690007 | ||||||
chr2:222690083
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.478+614T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690083 | ||||||
chr2:222690181
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.478+712G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690181 | ||||||
chr2:222690202
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.478+733C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690202 | ||||||
chr2:222690280
|
C | T | 1 | a0002c0002t0002g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478+811C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690280 | ||||||
chr2:222690454
|
A | G | 138 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 148 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.478+985A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690454 | ||||||
chr2:222690522
|
A | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0129others(3): Show | 7 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+1053A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690522 | ||||||
chr2:222690571
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0188others(6): Show | 11 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.478+1102G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690571 | ||||||
chr2:222690575
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.478+1106A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690575 | ||||||
chr2:222691004
|
G | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(4): Show | 8 | HG01496.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+1535G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691004 | ||||||
chr2:222691051
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.478+1582C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691051 | ||||||
chr2:222691067
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.478+1598A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691067 | ||||||
chr2:222691111
|
C | T | 8 | a0001c0001t0001g0124a0001c0001t0001g0263a0001c0001t0002g0049others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+1642C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691111 | ||||||
chr2:222691174
|
G | GTTTCTTT others(6): Show |
157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(154): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.478+1714_478+1715i others(15): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 222691174 | |||||
chr2:222691196
|
T | A | 15 | a0001c0001t0001g0050a0001c0001t0001g0124a0001c0001t0001g0143others(12): Show | 15 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.478+1727T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691196 | ||||||
chr2:222691199
|
A | T | 40 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0050others(37): Show | 44 | HG00642.hp1 HG00738.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.478+1730A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691199 | ||||||
chr2:222691214
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.478+1745A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691214 | ||||||
chr2:222691534
|
A | T | 72 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 78 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.478+2065A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691534 | ||||||
chr2:222691709
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.478+2240C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691709 | ||||||
chr2:222691810
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.478+2341A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691810 | ||||||
chr2:222691886
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.478+2417G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691886 | ||||||
chr2:222691979
|
G | T | 1 | a0001c0001t0001g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.479-2383G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691979 | ||||||
chr2:222692033
|
G | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0139others(15): Show | 20 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.479-2329G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692033 | ||||||
chr2:222692264
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.479-2098A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692264 | ||||||
chr2:222692328
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(69): Show | 78 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.479-2034A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692328 | ||||||
chr2:222692399
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.479-1963A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692399 | ||||||
chr2:222692563
|
C | T | 1 | a0002c0002t0002g0043 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.479-1799C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692563 | ||||||
chr2:222692608
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0139others(12): Show | 17 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.479-1754T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692608 | ||||||
chr2:222692662
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.479-1700T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692662 | ||||||
chr2:222692766
|
A | G | 1 | a0003c0003t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.479-1596A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692766 | ||||||
chr2:222692810
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(142): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.479-1552G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692810 | ||||||
chr2:222692814
|
G | A | 2 | a0001c0001t0001g0025a0002c0002t0001g0024 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.479-1548G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692814 | ||||||
chr2:222692984
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0195 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.479-1378C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692984 | ||||||
chr2:222693067
|
A | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0139others(12): Show | 17 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.479-1295A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693067 | ||||||
chr2:222693214
|
A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 12 | HG00597.hp2 HG02083.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.479-1148A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693214 | ||||||
chr2:222693339
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.479-1023A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693339 | ||||||
chr2:222693344
|
G | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0162a0001c0001t0001g0228others(1): Show | 4 | HG00673.hp2 HG02129.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-1018G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693344 | ||||||
chr2:222693448
|
GT | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(107): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.479-894delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 222693448 | |||||
chr2:222693448
|
GTT | G | 15 | a0001c0001t0001g0013a0001c0001t0001g0130a0001c0001t0001g0136others(12): Show | 16 | HG01496.hp2 HG01884.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.479-895_479-894del others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 222693448 | |||||
chr2:222693455
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.479-907T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693455 | ||||||
chr2:222693492
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.479-870T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693492 | ||||||
chr2:222693494
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.479-868A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693494 | ||||||
chr2:222693637
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.479-725G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693637 | ||||||
chr2:222693912
|
A | C | 1 | a0003c0003t0001g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.479-450A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693912 | ||||||
chr2:222693927
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.479-435G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693927 | ||||||
chr2:222693956
|
G | A | 20 | a0001c0001t0001g0087a0001c0001t0002g0002a0001c0001t0002g0028others(17): Show | 23 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.479-406G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693956 | ||||||
chr2:222693967
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0084 | 2 | NA18950.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.479-395C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693967 | ||||||
chr2:222694134
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.479-228G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222694134 | ||||||
chr2:222694171
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(119): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.479-191G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222694171 | ||||||
chr2:222694302
|
T | A | 1 | a0003c0003t0001g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.479-60T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222694302 | ||||||
chr2:222694329
|
G | T | 1 | a0002c0002t0002g0043 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.479-33G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222694329 | ||||||
chr2:222694599
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.653+63G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694599 | ||||||
chr2:222694633
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.653+97C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694633 | ||||||
chr2:222694779
|
C | T | 4 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0052others(1): Show | 5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+243C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694779 | ||||||
chr2:222694921
|
A | G | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.654-168A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694921 | ||||||
chr2:222694995
|
T | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.654-94T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694995 | ||||||
chr2:222695070
|
G | A | 1 | a0003c0003t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-19G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222695070 | ||||||
chr2:222695621
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.853+333T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695621 | ||||||
chr2:222695700
|
T | C | 1 | a0005c0005t0001g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.853+412T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695700 | ||||||
chr2:222695702
|
G | A | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+414G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695702 | ||||||
chr2:222695729
|
G | A | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+441G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695729 | ||||||
chr2:222695783
|
A | T | 1 | a0001c0001t0001g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.853+495A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695783 | ||||||
chr2:222695918
|
C | G | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+630C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695918 | ||||||
chr2:222696163
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.853+875C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696163 | ||||||
chr2:222696225
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.853+937C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696225 | ||||||
chr2:222696343
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.853+1055A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696343 | ||||||
chr2:222696501
|
T | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+1213T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696501 | ||||||
chr2:222696873
|
T | C | 6 | a0001c0001t0001g0163a0002c0002t0001g0023a0002c0002t0001g0138others(3): Show | 6 | HG01106.hp1 HG01109.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.853+1585T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696873 | ||||||
chr2:222696968
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(50): Show | 57 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.853+1680A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696968 | ||||||
chr2:222696987
|
C | T | 35 | a0001c0001t0001g0022a0001c0001t0001g0087a0001c0001t0001g0100others(32): Show | 36 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.853+1699C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696987 | ||||||
chr2:222697249
|
T | C | 1 | a0003c0003t0001g0277 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.853+1961T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697249 | ||||||
chr2:222697318
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.853+2030C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697318 | ||||||
chr2:222697348
|
C | T | 1 | a0005c0005t0001g0276 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853+2060C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697348 | ||||||
chr2:222697576
|
C | CT | 16 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0066others(13): Show | 17 | HG01109.hp1 HG01433.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.853+2311dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222697576 | |||||
chr2:222697576
|
CT | C | 25 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0096others(22): Show | 25 | HG00609.hp2 HG01106.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.853+2311delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222697576 | |||||
chr2:222697576
|
CTT | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(75): Show | 84 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.853+2310_853+2311d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222697576 | |||||
chr2:222697631
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.853+2343G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697631 | ||||||
chr2:222697659
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.853+2371C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697659 | ||||||
chr2:222697960
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0122others(23): Show | 32 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.853+2672C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697960 | ||||||
chr2:222698111
|
G | GT | 115 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(112): Show | 121 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.853+2827dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222698111 | |||||
chr2:222698118
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0195 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.853+2830T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698118 | ||||||
chr2:222698253
|
G | A | 1 | a0002c0002t0002g0047 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.853+2965G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698253 | ||||||
chr2:222698412
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.853+3124T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698412 | ||||||
chr2:222698495
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+3207G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698495 | ||||||
chr2:222698607
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.853+3319G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698607 | ||||||
chr2:222698766
|
T | A | 2 | a0001c0001t0001g0257a0002c0002t0001g0024 | 2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.853+3478T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698766 | ||||||
chr2:222698779
|
G | T | 3 | a0002c0002t0001g0193a0002c0002t0001g0211a0002c0002t0001g0253 | 3 | HG01952.hp1 NA19010.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.853+3491G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698779 | ||||||
chr2:222698812
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0137others(7): Show | 11 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.853+3524G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698812 | ||||||
chr2:222698855
|
G | A | 64 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0026others(61): Show | 68 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.853+3567G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698855 | ||||||
chr2:222698892
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0227 | 2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.853+3604C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698892 | ||||||
chr2:222698925
|
T | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(106): Show | 116 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.853+3637T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698925 | ||||||
chr2:222699002
|
C | CT | 8 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0091others(5): Show | 8 | HG02027.hp2 HG02738.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+3734dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699002 | |||||
chr2:222699002
|
CT | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0070others(53): Show | 63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.853+3734delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699002 | |||||
chr2:222699002
|
CTT | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0025others(35): Show | 41 | HG00099.hp2 HG00609.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.853+3733_853+3734d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699002 | |||||
chr2:222699002
|
CTTT | C | 66 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0026others(63): Show | 70 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.853+3732_853+3734d others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699002 | |||||
chr2:222699120
|
T | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(106): Show | 116 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.853+3832T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699120 | ||||||
chr2:222699292
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.853+4004G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699292 | ||||||
chr2:222699313
|
T | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+4025T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699313 | ||||||
chr2:222699392
|
T | G | 5 | a0001c0001t0001g0163a0002c0002t0001g0151a0002c0002t0001g0256others(2): Show | 5 | HG01106.hp1 HG01361.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+4104T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699392 | ||||||
chr2:222699402
|
A | G | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+4114A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699402 | ||||||
chr2:222699475
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | HG02055.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.853+4187T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699475 | ||||||
chr2:222699490
|
C | CT | 49 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0025others(46): Show | 52 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.853+4226dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | |||||
chr2:222699490
|
C | CTT | 9 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0093others(6): Show | 9 | HG01358.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+4225_853+4226d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | |||||
chr2:222699490
|
C | CTTT | 53 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0055others(50): Show | 56 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.853+4224_853+4226d others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | |||||
chr2:222699490
|
C | CTTTT | 11 | a0001c0001t0001g0077a0001c0001t0001g0133a0001c0001t0001g0143others(8): Show | 11 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.853+4223_853+4226d others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | |||||
chr2:222699490
|
CT | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0115others(3): Show | 6 | HG01167.hp1 HG02155.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+4226delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | |||||
chr2:222699520
|
G | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0127others(17): Show | 23 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.853+4232G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699520 | ||||||
chr2:222699645
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.853+4357C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699645 | ||||||
chr2:222699711
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.853+4423G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699711 | ||||||
chr2:222699832
|
T | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+4544T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699832 | ||||||
chr2:222699840
|
T | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+4552T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699840 | ||||||
chr2:222699859
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0177 | 2 | NA18952.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.853+4571C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699859 | ||||||
chr2:222699952
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.853+4664C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699952 | ||||||
chr2:222699957
|
T | C | 8 | a0001c0001t0001g0163a0002c0002t0001g0138a0002c0002t0001g0151others(5): Show | 8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+4669T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699957 | ||||||
chr2:222699963
|
A | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+4675A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699963 | ||||||
chr2:222700082
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.853+4794A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700082 | ||||||
chr2:222700354
|
G | T | 1 | a0001c0001t0001g0202 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.853+5066G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700354 | ||||||
chr2:222700546
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+5258G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700546 | ||||||
chr2:222700568
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.853+5280G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700568 | ||||||
chr2:222700657
|
C | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+5369C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700657 | ||||||
chr2:222700802
|
T | C | 3 | a0002c0002t0001g0138a0002c0002t0001g0262a0003c0003t0001g0282 | 3 | HG02451.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.853+5514T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700802 | ||||||
chr2:222700838
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.853+5550A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700838 | ||||||
chr2:222700872
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.853+5584G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700872 | ||||||
chr2:222700905
|
C | T | 67 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0055others(64): Show | 70 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.853+5617C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700905 | ||||||
chr2:222701111
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+5823G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701111 | ||||||
chr2:222701141
|
T | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0127others(17): Show | 23 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.853+5853T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701141 | ||||||
chr2:222701214
|
C | T | 8 | a0001c0001t0001g0163a0002c0002t0001g0138a0002c0002t0001g0151others(5): Show | 8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+5926C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701214 | ||||||
chr2:222701282
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.853+5994G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701282 | ||||||
chr2:222701287
|
A | AGGAG | 3 | a0002c0002t0001g0138a0002c0002t0001g0262a0003c0003t0001g0282 | 3 | HG02451.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.853+6000_853+6001i others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701287 | |||||
chr2:222701287
|
AGAG | A | 18 | a0001c0001t0001g0100a0001c0001t0001g0140a0001c0001t0001g0142others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.853+6012_853+6014d others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701287 | |||||
chr2:222701296
|
GGAGGA | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0195 | 3 | HG02615.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.853+6012_853+6016d others(7): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701296 | |||||
chr2:222701296
|
GGAGGAGA | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0092a0001c0001t0001g0132others(11): Show | 15 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.853+6012_853+6018d others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701296 | |||||
chr2:222701298
|
AG | A | 3 | a0001c0001t0001g0026a0002c0002t0002g0031a0002c0002t0002g0032 | 3 | HG00642.hp1 HG01261.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853+6012delG | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701298 | |||||
chr2:222701299
|
G | GA | 23 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0055others(20): Show | 24 | HG00609.hp2 HG01192.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | ||||||
chr2:222701299
|
G | GAGA | 11 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0208others(8): Show | 12 | HG00609.hp1 HG00735.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | ||||||
chr2:222701299
|
G | GAGAGA | 9 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0001g0234others(6): Show | 9 | HG01109.hp2 HG01928.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(7): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | ||||||
chr2:222701299
|
G | GAGAGAGA | 8 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0150others(5): Show | 10 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | ||||||
chr2:222701299
|
G | GAGAGAGA others(2): Show |
11 | a0001c0001t0001g0072a0001c0001t0001g0081a0001c0001t0001g0094others(8): Show | 11 | HG02257.hp1 HG02523.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(11): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | ||||||
chr2:222701299
|
G | GAGAGAGA others(4): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0093others(5): Show | 9 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(13): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | ||||||
chr2:222701299
|
G | GAGAGAGA others(6): Show |
1 | a0003c0003t0001g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.853+6011_853+6012i others(15): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | ||||||
chr2:222701299
|
G | GAGAGAGA others(8): Show |
2 | a0001c0001t0001g0204a0002c0002t0001g0152 | 2 | HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.853+6011_853+6012i others(17): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | ||||||
chr2:222701299
|
G | GGA | 8 | a0001c0001t0001g0007a0001c0001t0001g0097a0002c0002t0001g0123others(5): Show | 9 | HG00597.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+6040_853+6041d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701299 | |||||
chr2:222701299
|
G | GGAGAGAG others(5): Show |
1 | a0001c0001t0001g0096 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.853+6030_853+6041d others(14): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701299 | |||||
chr2:222701299
|
GGAGAGAG others(9): Show |
G | 2 | a0002c0002t0001g0135a0002c0002t0001g0175 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.853+6026_853+6041d others(18): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701299 | |||||
chr2:222701301
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0001g0085others(3): Show | 7 | HG02080.hp2 HG02083.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+6013A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701301 | ||||||
chr2:222701330
|
T | G | 67 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0055others(64): Show | 70 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.853+6042T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701330 | ||||||
chr2:222701394
|
A | G | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853+6106A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701394 | ||||||
chr2:222701398
|
A | AAG | 1 | a0001c0001t0001g0004 | 3 | HG02258.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.853+6124_853+6125d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701398 | |||||
chr2:222701398
|
A | G | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853+6110A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701398 | ||||||
chr2:222701414
|
A | G | 1 | a0009c0008t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.853+6126A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701414 | ||||||
chr2:222701421
|
A | T | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853+6133A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701421 | ||||||
chr2:222701487
|
A | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.853+6199A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701487 | ||||||
chr2:222701497
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.853+6209G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701497 | ||||||
chr2:222701537
|
A | AAGAG | 120 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 126 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.853+6252_853+6253i others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701537 | |||||
chr2:222701546
|
G | GA | 107 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(104): Show | 113 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.853+6264dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701546 | |||||
chr2:222701551
|
A | AAAGAAAG | 9 | a0001c0001t0001g0163a0002c0002t0001g0125a0002c0002t0001g0138others(6): Show | 9 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.853+6264_853+6265i others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701551 | |||||
chr2:222701561
|
G | GAAA | 8 | a0001c0001t0001g0163a0002c0002t0001g0138a0002c0002t0001g0151others(5): Show | 8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+6274_853+6275i others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701561 | |||||
chr2:222701571
|
G | A | 8 | a0001c0001t0001g0163a0002c0002t0001g0138a0002c0002t0001g0151others(5): Show | 8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+6283G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701571 | ||||||
chr2:222701572
|
A | AG | 8 | a0001c0001t0001g0163a0002c0002t0001g0138a0002c0002t0001g0151others(5): Show | 8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+6284_853+6285i others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701572 | ||||||
chr2:222701596
|
A | AAAAGAAA others(11): Show |
2 | a0001c0001t0001g0257a0002c0002t0001g0024 | 2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.853+6309_853+6310i others(20): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | |||||
chr2:222701596
|
A | AAAAGAAA others(19): Show |
1 | a0001c0001t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.853+6309_853+6310i others(28): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | |||||
chr2:222701596
|
A | AAAAGAGA others(9): Show |
2 | a0001c0001t0001g0204a0002c0002t0001g0258 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.853+6309_853+6310i others(18): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | |||||
chr2:222701596
|
A | AAAAGAGA others(13): Show |
99 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(96): Show | 105 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.853+6309_853+6310i others(22): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | |||||
chr2:222701596
|
A | AAAAGAGA others(17): Show |
3 | a0005c0005t0001g0274a0005c0005t0001g0275a0005c0005t0001g0276 | 3 | HG02109.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.853+6309_853+6310i others(26): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | |||||
chr2:222701596
|
A | AAGAAAGA others(17): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+6310_853+6311i others(26): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | |||||
chr2:222701630
|
C | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 126 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.853+6342C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701630 | ||||||
chr2:222701733
|
G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(105): Show | 114 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.853+6445G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701733 | ||||||
chr2:222702297
|
A | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.853+7009A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702297 | ||||||
chr2:222702307
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(154): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.853+7019C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702307 | ||||||
chr2:222702576
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0240 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.854-7160G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702576 | ||||||
chr2:222702832
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0147a0001c0001t0001g0167others(1): Show | 4 | NA18971.hp2 NA19010.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-6904A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702832 | ||||||
chr2:222702883
|
C | T | 6 | a0001c0001t0001g0163a0001c0001t0002g0049a0002c0002t0001g0151others(3): Show | 6 | HG01106.hp1 HG01361.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-6853C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702883 | ||||||
chr2:222702934
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.854-6802A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702934 | ||||||
chr2:222703403
|
T | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0049 | 3 | HG02055.hp1 HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.854-6333T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222703403 | ||||||
chr2:222703437
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.854-6299C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222703437 | ||||||
chr2:222703523
|
A | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0072others(20): Show | 25 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.854-6213A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222703523 | ||||||
chr2:222703738
|
C | T | 2 | a0005c0005t0001g0271a0009c0008t0001g0126 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.854-5998C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222703738 | ||||||
chr2:222703830
|
AT | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(115): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.854-5895delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222703830 | |||||
chr2:222703917
|
A | AC | 131 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(128): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.854-5817dupC | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222703917 | |||||
chr2:222704054
|
A | G | 1 | a0002c0002t0002g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.854-5682A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704054 | ||||||
chr2:222704109
|
T | C | 2 | a0005c0005t0001g0271a0009c0008t0001g0126 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.854-5627T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704109 | ||||||
chr2:222704183
|
T | C | 2 | a0001c0001t0001g0213a0003c0003t0001g0287 | 2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.854-5553T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704183 | ||||||
chr2:222704291
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.854-5445G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704291 | ||||||
chr2:222704451
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0221a0001c0001t0002g0037 | 3 | HG00280.hp2 HG01346.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.854-5285C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704451 | ||||||
chr2:222704481
|
G | A | 2 | a0005c0005t0001g0271a0009c0008t0001g0126 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.854-5255G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704481 | ||||||
chr2:222704485
|
G | A | 3 | a0002c0002t0001g0138a0002c0002t0001g0262a0003c0003t0001g0282 | 3 | HG02451.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.854-5251G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704485 | ||||||
chr2:222704486
|
T | A | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854-5250T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704486 | ||||||
chr2:222704492
|
T | C | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854-5244T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704492 | ||||||
chr2:222704495
|
A | G | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854-5241A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704495 | ||||||
chr2:222704503
|
A | G | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854-5233A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704503 | ||||||
chr2:222704579
|
G | C | 2 | a0002c0002t0001g0138a0002c0002t0001g0262 | 2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.854-5157G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704579 | ||||||
chr2:222704618
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0092a0001c0001t0001g0159 | 4 | HG02027.hp1 NA18972.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-5118C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704618 | ||||||
chr2:222704627
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.854-5109A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704627 | ||||||
chr2:222704856
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.854-4880G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704856 | ||||||
chr2:222704909
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.854-4827C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704909 | ||||||
chr2:222704989
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0180a0003c0003t0001g0291 | 3 | HG02257.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.854-4747T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704989 | ||||||
chr2:222705138
|
A | G | 1 | a0003c0003t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.854-4598A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705138 | ||||||
chr2:222705161
|
A | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.854-4575A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705161 | ||||||
chr2:222705414
|
C | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.854-4322C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705414 | ||||||
chr2:222705442
|
C | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0074a0001c0001t0001g0233 | 4 | NA18954.hp2 NA18970.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-4294C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705442 | ||||||
chr2:222705473
|
G | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0051others(8): Show | 12 | HG01106.hp1 HG01243.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.854-4263G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705473 | ||||||
chr2:222705624
|
GT | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0129 | 4 | HG01243.hp1 HG02965.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-4109delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222705624 | |||||
chr2:222705659
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.854-4077T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705659 | ||||||
chr2:222705728
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | NA18950.hp1 NA18984.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.854-4008C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705728 | ||||||
chr2:222706023
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.854-3713G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706023 | ||||||
chr2:222706114
|
A | C | 1 | a0006c0006t0001g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.854-3622A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706114 | ||||||
chr2:222706294
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.854-3442G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706294 | ||||||
chr2:222706344
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0129 | 4 | HG01243.hp1 HG02965.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-3392G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706344 | ||||||
chr2:222706469
|
T | C | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.854-3267T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706469 | ||||||
chr2:222706471
|
T | TA | 129 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.854-3249dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222706471 | |||||
chr2:222706488
|
T | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.854-3248T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706488 | ||||||
chr2:222706496
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.854-3240A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706496 | ||||||
chr2:222706511
|
T | C | 4 | a0002c0002t0001g0125a0002c0002t0001g0138a0002c0002t0001g0262others(1): Show | 4 | HG02451.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-3225T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706511 | ||||||
chr2:222706518
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.854-3218T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706518 | ||||||
chr2:222706691
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.854-3045A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706691 | ||||||
chr2:222706726
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(132): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.854-3010A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706726 | ||||||
chr2:222706850
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0195a0001c0001t0002g0049 | 3 | HG02615.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.854-2886G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706850 | ||||||
chr2:222706868
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.854-2868C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706868 | ||||||
chr2:222706966
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.854-2770A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706966 | ||||||
chr2:222707110
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.854-2626T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707110 | ||||||
chr2:222707219
|
C | CAAGG | 8 | a0001c0001t0001g0012a0001c0001t0001g0055a0001c0001t0001g0127others(5): Show | 9 | HG01243.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.854-2500_854-2497d others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707219 | |||||
chr2:222707281
|
GGGAA | G | 3 | a0001c0001t0001g0163a0004c0004t0001g0241a0004c0004t0001g0242 | 3 | HG01168.hp1 HG01169.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.854-2438_854-2435d others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707281 | |||||
chr2:222707337
|
AAGAAAGA others(17): Show |
A | 1 | a0001c0001t0001g0096 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.854-2387_854-2364d others(26): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707337 | |||||
chr2:222707339
|
GAAAGAAA others(3): Show |
G | 15 | a0001c0001t0001g0022a0001c0001t0001g0087a0001c0001t0001g0192others(12): Show | 16 | HG01433.hp1 HG01515.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.854-2385_854-2376d others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707339 | |||||
chr2:222707349
|
A | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0025others(37): Show | 43 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.854-2387A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707349 | ||||||
chr2:222707351
|
A | G | 1 | a0003c0003t0001g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.854-2385A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707351 | ||||||
chr2:222707351
|
AAGAAAGA others(3): Show |
A | 41 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0025others(38): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.854-2363_854-2354d others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707351 | |||||
chr2:222707361
|
G | GAGAA | 81 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0050others(78): Show | 84 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.854-2367_854-2364d others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707361 | |||||
chr2:222707361
|
GAGAAAGA others(7): Show |
G | 1 | a0003c0003t0001g0283 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.854-2365_854-2352d others(16): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707361 | |||||
chr2:222707371
|
G | GAAAT | 11 | a0001c0001t0001g0012a0001c0001t0001g0055a0001c0001t0001g0127others(8): Show | 12 | HG01243.hp1 HG01496.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.854-2364_854-2363i others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707371 | |||||
chr2:222707394
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0264 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.854-2342A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707394 | ||||||
chr2:222707395
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0264 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.854-2341A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707395 | ||||||
chr2:222707397
|
GAGGGAGG others(2): Show |
G | 9 | a0001c0001t0001g0163a0001c0001t0001g0257a0002c0002t0001g0024others(6): Show | 9 | HG01106.hp1 HG01361.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.854-2313_854-2305d others(11): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707397 | |||||
chr2:222707457
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.854-2279A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707457 | ||||||
chr2:222707672
|
C | A | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.854-2064C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707672 | ||||||
chr2:222707698
|
A | C | 5 | a0001c0001t0001g0163a0002c0002t0001g0151a0002c0002t0001g0256others(2): Show | 5 | HG01106.hp1 HG01361.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.854-2038A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707698 | ||||||
chr2:222707892
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.854-1844T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707892 | ||||||
chr2:222707909
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0068a0001c0001t0001g0111others(3): Show | 7 | HG02129.hp1 NA18945.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.854-1827A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707909 | ||||||
chr2:222708066
|
C | CT | 15 | a0001c0001t0001g0055a0001c0001t0001g0101a0001c0001t0001g0124others(12): Show | 15 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.854-1662dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222708066 | |||||
chr2:222708142
|
G | A | 1 | a0002c0002t0001g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.854-1594G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708142 | ||||||
chr2:222708301
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.854-1435A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708301 | ||||||
chr2:222708367
|
A | G | 2 | a0001c0001t0001g0213a0003c0003t0001g0287 | 2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.854-1369A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708367 | ||||||
chr2:222708460
|
G | A | 5 | a0001c0001t0001g0163a0002c0002t0001g0151a0002c0002t0001g0256others(2): Show | 5 | HG01106.hp1 HG01361.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.854-1276G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708460 | ||||||
chr2:222708570
|
G | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0124a0001c0001t0001g0137others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.854-1166G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708570 | ||||||
chr2:222708591
|
C | T | 3 | a0002c0002t0001g0023a0003c0003t0001g0282a0009c0008t0001g0126 | 3 | HG01109.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.854-1145C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708591 | ||||||
chr2:222708815
|
TTGTG | T | 3 | a0001c0001t0001g0181a0001c0001t0002g0002a0001c0001t0002g0046 | 6 | HG02622.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-919_854-916del others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222708815 | |||||
chr2:222708875
|
T | C | 1 | a0001c0011t0001g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.854-861T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708875 | ||||||
chr2:222709026
|
A | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(104): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.854-710A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709026 | ||||||
chr2:222709107
|
G | A | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.854-629G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709107 | ||||||
chr2:222709358
|
T | G | 1 | a0002c0002t0001g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.854-378T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709358 | ||||||
chr2:222709401
|
T | A | 6 | a0001c0001t0001g0163a0002c0002t0001g0119a0002c0002t0001g0151others(3): Show | 6 | HG01106.hp1 HG01361.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-335T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709401 | ||||||
chr2:222709721
|
T | A | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.854-15T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709721 |