geneid | 79796 |
---|---|
ensemblid | ENSG00000086848.15 |
hgncid | 15672 |
symbol | ALG9 |
name | ALG9 alpha-1,2-mannosyltransferase |
refseq_nuc | NM_024740.2 |
refseq_prot | NP_079016.2 |
ensembl_nuc | ENST00000616540.5 |
ensembl_prot | ENSP00000482437.1 |
mane_status | MANE Select |
chr | chr11 |
start | 111782195 |
end | 111871581 |
strand | - |
ver | v1.2 |
region | chr11:111782195-111871581 |
region5000 | chr11:111777195-111876581 |
regionname0 | ALG9_chr11_111782195_111871581 |
regionname5000 | ALG9_chr11_111777195_111876581 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 618 | 203 | 65 | 44 | 62 | 11 | 19 | 49 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0002 | 0/0 | 618 | 97 | 15 | 16 | 50 | 1 | 15 | 38 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0003 | 0/0 | 618 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0004 | 0/0 | 618 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0005 | 0/0 | 618 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0006 | 0/0 | 618 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0007 | 0/0 | 618 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1857 | 198 | 62 | 44 | 60 | 11 | 19 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0002 | 0/0 | 1857 | 97 | 15 | 16 | 50 | 1 | 15 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0003 | 0/0 | 1857 | 6 | 6 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0004 | 0/0 | 1857 | 4 | 0 | 0 | 4 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0005 | 0/0 | 1857 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0006 | 0/0 | 1857 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0007 | 0/0 | 1857 | 2 | 1 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0008 | 0/0 | 1857 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0009 | 0/0 | 1857 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
c0010 | 0/0 | 1857 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4302 | 89 | 11 | 16 | 46 | 2 | 14 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0002 | 1/1 | 4302 | 74 | 8 | 17 | 31 | 3 | 13 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0003 | 0/0 | 4289 | 64 | 12 | 17 | 25 | 5 | 5 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0004 | 0/0 | 4301 | 20 | 14 | 1 | 5 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0005 | 0/0 | 4303 | 16 | 12 | 4 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0006 | 0/0 | 4302 | 4 | 4 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0007 | 0/0 | 4289 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0008 | 0/0 | 4288 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0009 | 0/0 | 4302 | 3 | 2 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0010 | 0/0 | 4303 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0011 | 0/0 | 4302 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0012 | 0/0 | 4302 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0013 | 0/0 | 4302 | 2 | 0 | 0 | 0 | 1 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0014 | 0/0 | 4288 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0015 | 0/0 | 4302 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0016 | 0/0 | 4302 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0017 | 0/0 | 4289 | 2 | 0 | 1 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0018 | 0/0 | 4302 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0019 | 0/0 | 4289 | 2 | 0 | 1 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0020 | 0/0 | 4302 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0021 | 0/0 | 4302 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0022 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0023 | 0/0 | 4288 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0024 | 0/0 | 4302 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0025 | 0/0 | 4302 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0026 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0027 | 0/0 | 4301 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0028 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0029 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0030 | 0/0 | 4302 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0031 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
t0032 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1857 | 198 | 62 | 44 | 60 | 11 | 19 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0005 | 0/0 | 1857 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0006 | 0/0 | 1857 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0010 | 0/0 | 1857 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0002c0002 | 0/0 | 1857 | 97 | 15 | 16 | 50 | 1 | 15 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0003c0003 | 0/0 | 1857 | 6 | 6 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0004c0004 | 0/0 | 1857 | 4 | 0 | 0 | 4 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0005c0007 | 0/0 | 1857 | 2 | 1 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0006c0008 | 0/0 | 1857 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0007c0009 | 0/0 | 1857 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6158 | 6 | 5 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0002 | 1/1 | 6158 | 71 | 5 | 17 | 31 | 3 | 13 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0003 | 0/0 | 6145 | 62 | 12 | 17 | 23 | 5 | 5 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0004 | 0/0 | 6157 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0005 | 0/0 | 6159 | 16 | 12 | 4 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0006 | 0/0 | 6158 | 4 | 4 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0007 | 0/0 | 6145 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0008 | 0/0 | 6144 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0009 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0010 | 0/0 | 6159 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0011 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0012 | 0/0 | 6158 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0013 | 0/0 | 6158 | 2 | 0 | 0 | 0 | 1 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0014 | 0/0 | 6144 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0015 | 0/0 | 6158 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0016 | 0/0 | 6158 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0017 | 0/0 | 6145 | 2 | 0 | 1 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0018 | 0/0 | 6158 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0019 | 0/0 | 6145 | 2 | 0 | 1 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0020 | 0/0 | 6158 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0022 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0023 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0024 | 0/0 | 6158 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0025 | 0/0 | 6158 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0028 | 0/0 | 6159 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0029 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0031 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0001t0032 | 0/0 | 6159 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0005t0011 | 0/0 | 6158 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0006t0003 | 0/0 | 6145 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0001c0010t0002 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0002c0002t0001 | 0/0 | 6158 | 74 | 2 | 15 | 42 | 1 | 14 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0002c0002t0002 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0002c0002t0004 | 0/0 | 6157 | 18 | 12 | 1 | 5 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0002c0002t0021 | 0/0 | 6158 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0002c0002t0027 | 0/0 | 6157 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0002c0002t0030 | 0/0 | 6158 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0003c0003t0001 | 0/0 | 6158 | 4 | 4 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0003c0003t0004 | 0/0 | 6157 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0003c0003t0026 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0004c0004t0001 | 0/0 | 6158 | 4 | 0 | 0 | 4 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0005c0007t0009 | 0/0 | 6158 | 2 | 1 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0006c0008t0001 | 0/0 | 6158 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
a0007c0009t0002 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | copy fasta | chr11 | 111777195 | 111876581 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0013g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0014g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0014g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0015g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0016g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0016g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0017g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0017g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0018g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0018g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0019g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0019g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0020g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0020g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0022g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0023g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0024g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0028g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0029g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0031g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0001t0032g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0005t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0005t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0006t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0006t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0001c0010t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0021g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0021g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0027g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0002c0002t0030g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0003c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0003c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0003c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0003c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0003c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0003c0003t0026g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0004c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0004c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0004c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0004c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0005c0007t0009g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0005c0007t0009g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0006c0008t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
a0007c0009t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0013 | g0165 | EUR | GBR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0256 | EUR | GBR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0210 | EUR | GBR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00597 | hp1 | a0004 | c0004 | t0001 | g0099 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00621 | hp2 | a0002 | c0002 | t0021 | g0068 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00733 | hp2 | a0001 | c0001 | t0018 | g0302 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00735 | hp1 | a0001 | c0001 | t0017 | g0234 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00735 | hp2 | a0006 | c0008 | t0001 | g0057 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01099 | hp1 | a0001 | c0001 | t0018 | g0301 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0121 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01256 | hp2 | a0001 | c0001 | t0014 | g0224 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0226 | EUR | IBS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0159 | EUR | IBS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | IBS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0271 | EUR | IBS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0124 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0106 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0231 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01952 | hp1 | a0005 | c0007 | t0009 | g0286 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01978 | hp1 | a0001 | c0001 | t0019 | g0220 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01993 | hp1 | a0002 | c0002 | t0004 | g0075 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02055 | hp1 | a0002 | c0002 | t0004 | g0103 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02129 | hp2 | a0001 | c0001 | t0024 | g0148 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0263 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02145 | hp2 | a0001 | c0005 | t0011 | g0200 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | CDX | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02257 | hp2 | a0002 | c0002 | t0004 | g0100 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0126 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02300 | hp1 | a0001 | c0001 | t0014 | g0223 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0081 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02523 | hp1 | a0001 | c0001 | t0025 | g0133 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02572 | hp1 | a0001 | c0001 | t0020 | g0108 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02615 | hp1 | a0002 | c0002 | t0004 | g0101 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02630 | hp1 | a0001 | c0005 | t0011 | g0132 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02630 | hp2 | a0001 | c0001 | t0032 | g0112 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0091 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0288 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02818 | hp2 | a0002 | c0002 | t0004 | g0104 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02886 | hp2 | a0001 | c0001 | t0015 | g0146 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02895 | hp1 | a0001 | c0001 | t0010 | g0290 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0199 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02896 | hp1 | a0002 | c0002 | t0004 | g0086 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0196 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0197 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0289 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02922 | hp2 | a0001 | c0001 | t0016 | g0127 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0285 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02976 | hp1 | a0003 | c0003 | t0004 | g0122 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02976 | hp2 | a0001 | c0001 | t0016 | g0128 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0296 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03130 | hp1 | a0001 | c0001 | t0020 | g0107 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03130 | hp2 | a0001 | c0001 | t0028 | g0113 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03139 | hp1 | a0007 | c0009 | t0002 | g0131 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03209 | hp1 | a0001 | c0001 | t0015 | g0203 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03209 | hp2 | a0002 | c0002 | t0004 | g0087 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03453 | hp2 | a0001 | c0001 | t0022 | g0140 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03516 | hp1 | a0005 | c0007 | t0009 | g0284 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03579 | hp2 | a0001 | c0001 | t0031 | g0109 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0045 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03834 | hp1 | a0002 | c0002 | t0030 | g0082 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0254 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03942 | hp2 | a0001 | c0001 | t0013 | g0153 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0266 | SAS | STU | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | STU | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0240 | SAS | STU | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0056 | SAS | STU | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | YRI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | YRI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CHB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18943 | hp1 | a0001 | c0006 | t0003 | g0257 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18954 | hp2 | a0002 | c0002 | t0027 | g0059 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18956 | hp1 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18968 | hp2 | a0004 | c0004 | t0001 | g0098 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18969 | hp2 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18974 | hp2 | a0001 | c0001 | t0008 | g0264 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18978 | hp1 | a0002 | c0002 | t0021 | g0011 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18982 | hp1 | a0002 | c0002 | t0004 | g0079 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18982 | hp2 | a0001 | c0001 | t0008 | g0216 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18985 | hp2 | a0001 | c0001 | t0008 | g0228 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18989 | hp2 | a0004 | c0004 | t0001 | g0096 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19000 | hp1 | a0001 | c0006 | t0003 | g0261 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19002 | hp2 | a0001 | c0001 | t0019 | g0243 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19010 | hp1 | a0002 | c0002 | t0004 | g0054 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19043 | hp1 | a0003 | c0003 | t0026 | g0141 | AFR | LWK | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | LWK | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19076 | hp2 | a0002 | c0002 | t0004 | g0036 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19084 | hp2 | a0004 | c0004 | t0001 | g0097 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19240 | hp1 | a0003 | c0003 | t0001 | g0125 | AFR | YRI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ASW | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA20129 | hp2 | a0001 | c0010 | t0002 | g0206 | AFR | ASW | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | TSI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA20752 | hp2 | a0001 | c0001 | t0017 | g0272 | EUR | TSI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0273 | EUR | TSI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0042 | EUR | TSI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02109 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02109 | hp2 | a0002 | c0002 | t0004 | g0102 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0129 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02486 | hp2 | a0002 | c0002 | t0004 | g0105 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0244 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03471 | hp1 | a0001 | c0001 | t0029 | g0012 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | USA | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
HG06807 | hp2 | a0003 | c0003 | t0001 | g0123 | AFR | USA | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | USA | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA20300 | hp2 | a0002 | c0002 | t0004 | g0022 | AFR | USA | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA21309 | hp1 | a0001 | c0001 | t0023 | g0269 | AFR | LWK | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
NA21309 | hp2 | a0002 | c0002 | t0004 | g0300 | AFR | LWK | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0204 | REF | REF | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0136 | REF | REF | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111786462
|
A | G | 1 | a0007 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.1792T>C | p.Tyr598His | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1891/6158 | 1792/1857 | 598/618 | chr11 | 111786462 | ||
chr11:111809772
|
A | C | 1 | a0004 | 4 | HG00597.hp1 NA18968.hp2 NA18989.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1604T>G | p.Ile535Ser | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/15 | 1703/6158 | 1604/1857 | 535/618 | chr11 | 111809772 | ||
chr11:111836229
|
G | A | 1 | a0006 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1538C>T | p.Pro513Leu | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/15 | 1637/6158 | 1538/1857 | 513/618 | chr11 | 111836229 | ||
chr11:111853410
|
C | T | 3 | a0002a0004a0006 | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
missense_variant | MODERATE | c.865G>A | p.Val289Ile | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/15 | 964/6158 | 865/1857 | 289/618 | chr11 | 111853410 | ||
chr11:111853460
|
T | C | 1 | a0005 | 2 | HG01952.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.815A>G | p.Tyr272Cys | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/15 | 914/6158 | 815/1857 | 272/618 | chr11 | 111853460 | ||
chr11:111853674
|
G | A | 1 | a0003 | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
missense_variant | MODERATE | c.764C>T | p.Ser255Leu | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 7/15 | 863/6158 | 764/1857 | 255/618 | chr11 | 111853674 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111786460
|
G | A | 1 | a0001c0005 | 2 | HG02145.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.1794C>T | p.Tyr598Tyr | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1893/6158 | 1794/1857 | 598/618 | chr11 | 111786460 | ||
chr11:111809717
|
G | A | 1 | a0001c0006 | 2 | NA18943.hp1 NA19000.hp1 |
synonymous_variant | LOW | c.1659C>T | p.Pro553Pro | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/15 | 1758/6158 | 1659/1857 | 553/618 | chr11 | 111809717 | ||
chr11:111837557
|
G | A | 1 | a0001c0010 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1383C>T | p.Thr461Thr | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/15 | 1482/6158 | 1383/1857 | 461/618 | chr11 | 111837557 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111782432
|
C | T | 1 | a0001c0001t0015 | 2 | HG02886.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3965G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3965 | chr11 | 111782432 | |||||
chr11:111782647
|
T | G | 2 | a0001c0001t0009a0005c0007t0009 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3750A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3750 | chr11 | 111782647 | |||||
chr11:111782899
|
C | T | 1 | a0001c0001t0024 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3498 | chr11 | 111782899 | |||||
chr11:111782900
|
G | A | 1 | a0001c0001t0025 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3497C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3497 | chr11 | 111782900 | |||||
chr11:111782926
|
T | C | 1 | a0001c0001t0012 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3471A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3471 | chr11 | 111782926 | |||||
chr11:111782974
|
A | G | 1 | a0003c0003t0026 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3423T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3423 | chr11 | 111782974 | |||||
chr11:111783054
|
T | C | 1 | a0001c0001t0028 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3343A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3343 | chr11 | 111783054 | |||||
chr11:111783505
|
C | T | 1 | a0001c0001t0029 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2892G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2892 | chr11 | 111783505 | |||||
chr11:111783657
|
C | G | 1 | a0001c0001t0029 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2740G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2740 | chr11 | 111783657 | |||||
chr11:111783896
|
CTATAT | C | 8 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(5): Show | 77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2496_*2500delATAT others(1): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2496 | chr11 | 111783896 | |||||
chr11:111783917
|
GT | G | 4 | a0001c0001t0004a0002c0002t0004a0002c0002t0027others(1): Show | 21 | HG01891.hp1 HG01993.hp1 HG02055.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2479delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2479 | chr11 | 111783917 | |||||
chr11:111783922
|
T | A | 1 | a0001c0001t0016 | 2 | HG02922.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2475A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2475 | chr11 | 111783922 | |||||
chr11:111783923
|
T | A | 7 | a0001c0001t0011a0001c0001t0015a0001c0001t0016others(4): Show | 11 | HG00733.hp2 HG01099.hp1 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2474A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2474 | chr11 | 111783923 | |||||
chr11:111783923
|
T | TA | 6 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(3): Show | 74 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2473_*2474insT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2473 | chr11 | 111783923 | |||||
chr11:111783924
|
T | A | 31 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(28): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2473A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2473 | chr11 | 111783924 | |||||
chr11:111783940
|
C | A | 1 | a0002c0002t0027 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2457G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2457 | chr11 | 111783940 | |||||
chr11:111783945
|
TGACAAAA others(2): Show |
T | 8 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(5): Show | 77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2443_*2451delTGTT others(5): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2443 | chr11 | 111783945 | |||||
chr11:111784167
|
T | G | 1 | a0001c0001t0012 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2230A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2230 | chr11 | 111784167 | |||||
chr11:111784457
|
C | T | 1 | a0001c0001t0020 | 2 | HG02572.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1940G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1940 | chr11 | 111784457 | |||||
chr11:111784549
|
C | T | 1 | a0001c0001t0013 | 2 | HG00099.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1848G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1848 | chr11 | 111784549 | |||||
chr11:111784717
|
C | A | 1 | a0001c0001t0017 | 2 | HG00735.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1680G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1680 | chr11 | 111784717 | |||||
chr11:111784717
|
C | CA | 3 | a0001c0001t0005a0001c0001t0028a0001c0001t0032 | 18 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1679dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1679 | chr11 | 111784717 | |||||
chr11:111784726
|
A | G | 1 | a0001c0001t0007 | 3 | HG01891.hp2 HG02145.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1671 | chr11 | 111784726 | |||||
chr11:111784773
|
T | G | 1 | a0001c0001t0018 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1624A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1624 | chr11 | 111784773 | |||||
chr11:111784790
|
G | A | 2 | a0001c0001t0018a0001c0001t0029 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1607C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1607 | chr11 | 111784790 | |||||
chr11:111784977
|
G | C | 1 | a0001c0001t0019 | 2 | HG01978.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1420C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1420 | chr11 | 111784977 | |||||
chr11:111784995
|
A | G | 1 | a0001c0001t0020 | 2 | HG02572.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1402T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1402 | chr11 | 111784995 | |||||
chr11:111785056
|
C | T | 1 | a0001c0001t0022 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1341G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1341 | chr11 | 111785056 | |||||
chr11:111785177
|
G | A | 3 | a0001c0001t0006a0001c0001t0020a0001c0001t0031 | 7 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1220C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1220 | chr11 | 111785177 | |||||
chr11:111785426
|
G | A | 1 | a0002c0002t0021 | 2 | HG00621.hp2 NA18978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*971C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 971 | chr11 | 111785426 | |||||
chr11:111785609
|
T | C | 1 | a0002c0002t0030 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 788 | chr11 | 111785609 | |||||
chr11:111785728
|
G | T | 1 | a0001c0001t0006 | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*669C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 669 | chr11 | 111785728 | |||||
chr11:111786074
|
T | C | 1 | a0001c0001t0031 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*323A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 323 | chr11 | 111786074 | |||||
chr11:111786388
|
G | A | 1 | a0001c0001t0032 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 9 | chr11 | 111786388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111786568
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1734-48A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111786568 | ||||||
chr11:111786735
|
A | C | 1 | a0001c0001t0015g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1734-215T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111786735 | ||||||
chr11:111786757
|
A | C | 1 | a0001c0001t0003g0217 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1734-237T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111786757 | ||||||
chr11:111787042
|
A | G | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1734-522T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787042 | ||||||
chr11:111787126
|
C | T | 1 | a0001c0001t0003g0229 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1734-606G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787126 | ||||||
chr11:111787310
|
G | A | 2 | a0001c0001t0003g0215a0001c0001t0008g0216 | 2 | NA18965.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1734-790C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787310 | ||||||
chr11:111787419
|
C | G | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1734-899G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787419 | ||||||
chr11:111787419
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1734-899G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787419 | ||||||
chr11:111787450
|
T | A | 1 | a0002c0002t0001g0295 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1734-930A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787450 | ||||||
chr11:111787451
|
A | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-931T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787451 | ||||||
chr11:111787488
|
G | A | 1 | a0002c0002t0004g0086 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1734-968C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787488 | ||||||
chr11:111787557
|
C | T | 5 | a0001c0001t0011g0129a0001c0001t0016g0127a0001c0001t0016g0128others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-1037G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787557 | ||||||
chr11:111787735
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-1215C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787735 | ||||||
chr11:111787939
|
T | C | 1 | a0002c0002t0001g0069 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1734-1419A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787939 | ||||||
chr11:111788159
|
C | A | 1 | a0002c0002t0001g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1734-1639G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788159 | ||||||
chr11:111788188
|
G | A | 2 | a0001c0001t0002g0009a0001c0001t0002g0195 | 3 | HG01255.hp2 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1734-1668C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788188 | ||||||
chr11:111788264
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1734-1744G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788264 | ||||||
chr11:111788358
|
A | G | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1734-1838T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788358 | ||||||
chr11:111788387
|
T | C | 76 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0210others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1734-1867A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788387 | ||||||
chr11:111788752
|
C | A | 301 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(298): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1734-2232G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788752 | ||||||
chr11:111789000
|
C | T | 7 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1734-2480G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789000 | ||||||
chr11:111789019
|
TC | T | 97 | a0001c0001t0001g0212a0001c0001t0004g0110a0002c0002t0001g0001others(94): Show | 101 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1734-2500delG | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789019 | ||||||
chr11:111789020
|
C | T | 111 | a0001c0001t0001g0014a0001c0001t0003g0010a0001c0001t0003g0013others(108): Show | 113 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1734-2500G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789020 | ||||||
chr11:111789070
|
T | C | 4 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0005g0298others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734-2550A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789070 | ||||||
chr11:111789103
|
A | G | 1 | a0001c0001t0002g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1734-2583T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789103 | ||||||
chr11:111789200
|
A | G | 230 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(227): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1734-2680T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789200 | ||||||
chr11:111789285
|
T | C | 2 | a0001c0001t0003g0262a0001c0001t0003g0277 | 2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1734-2765A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789285 | ||||||
chr11:111789286
|
C | G | 1 | a0002c0002t0001g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1734-2766G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789286 | ||||||
chr11:111789296
|
T | A | 4 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012others(1): Show | 4 | HG00733.hp2 HG01099.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734-2776A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789296 | ||||||
chr11:111789515
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1734-2995G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789515 | ||||||
chr11:111789653
|
T | C | 1 | a0001c0001t0003g0270 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1734-3133A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789653 | ||||||
chr11:111789718
|
G | A | 3 | a0001c0001t0002g0161a0001c0001t0002g0167a0001c0001t0002g0193 | 3 | HG01256.hp1 HG01258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1734-3198C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789718 | ||||||
chr11:111789743
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1734-3223G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789743 | ||||||
chr11:111789819
|
C | CA | 6 | a0002c0002t0001g0003a0002c0002t0001g0037a0002c0002t0001g0038others(3): Show | 7 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1734-3300dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789819 | ||||||
chr11:111789988
|
T | A | 1 | a0002c0002t0001g0048 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1734-3468A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789988 | ||||||
chr11:111790201
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-3681C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790201 | ||||||
chr11:111790269
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1734-3749C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790269 | ||||||
chr11:111790626
|
T | C | 1 | a0001c0001t0003g0215 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1734-4106A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790626 | ||||||
chr11:111790663
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-4143C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790663 | ||||||
chr11:111790731
|
C | G | 204 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0003g0010others(201): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1734-4211G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790731 | ||||||
chr11:111790962
|
A | T | 230 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(227): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1734-4442T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790962 | ||||||
chr11:111791000
|
C | G | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-4480G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791000 | ||||||
chr11:111791385
|
C | T | 92 | a0001c0001t0001g0212a0001c0001t0004g0110a0002c0002t0001g0001others(89): Show | 96 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1734-4865G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791385 | ||||||
chr11:111791429
|
C | T | 6 | a0002c0002t0001g0055a0002c0002t0001g0061a0002c0002t0001g0078others(3): Show | 6 | HG02056.hp2 HG02155.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734-4909G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791429 | ||||||
chr11:111791600
|
T | C | 1 | a0001c0001t0006g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1734-5080A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791600 | ||||||
chr11:111791840
|
C | A | 75 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0210others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1734-5320G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791840 | ||||||
chr11:111791849
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1734-5329A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791849 | ||||||
chr11:111791860
|
G | A | 22 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(19): Show | 22 | HG01952.hp1 HG02145.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1734-5340C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791860 | ||||||
chr11:111791887
|
T | C | 13 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1734-5367A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791887 | ||||||
chr11:111791980
|
G | A | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1734-5460C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791980 | ||||||
chr11:111792190
|
C | T | 1 | a0001c0001t0017g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1734-5670G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792190 | ||||||
chr11:111792194
|
A | G | 19 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(16): Show | 19 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1734-5674T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792194 | ||||||
chr11:111792436
|
C | T | 19 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(16): Show | 19 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1734-5916G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792436 | ||||||
chr11:111792504
|
C | T | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-5984G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792504 | ||||||
chr11:111792979
|
T | C | 1 | a0001c0001t0003g0256 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1734-6459A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792979 | ||||||
chr11:111793193
|
A | G | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-6673T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793193 | ||||||
chr11:111793322
|
T | C | 2 | a0001c0001t0003g0281a0001c0001t0003g0283 | 2 | NA18977.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1734-6802A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793322 | ||||||
chr11:111793453
|
A | C | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1734-6933T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793453 | ||||||
chr11:111793479
|
G | A | 2 | a0001c0001t0002g0135a0001c0001t0002g0202 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1734-6959C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793479 | ||||||
chr11:111793496
|
T | C | 3 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0005g0299 | 3 | HG02723.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1734-6976A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793496 | ||||||
chr11:111793556
|
G | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-7036C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793556 | ||||||
chr11:111793557
|
C | G | 1 | a0004c0004t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1734-7037G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793557 | ||||||
chr11:111793558
|
A | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-7038T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793558 | ||||||
chr11:111793589
|
T | G | 1 | a0002c0002t0004g0026 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1734-7069A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793589 | ||||||
chr11:111793632
|
G | A | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-7112C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793632 | ||||||
chr11:111793633
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1734-7113A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793633 | ||||||
chr11:111793677
|
C | T | 75 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0210others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1734-7157G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793677 | ||||||
chr11:111793693
|
G | A | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1734-7173C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793693 | ||||||
chr11:111793757
|
G | C | 1 | a0001c0001t0002g0201 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1734-7237C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793757 | ||||||
chr11:111793760
|
C | CA | 23 | a0001c0001t0002g0192a0001c0001t0003g0258a0001c0001t0005g0005others(20): Show | 24 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1734-7241dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793760 | ||||||
chr11:111794085
|
C | T | 4 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734-7565G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794085 | ||||||
chr11:111794086
|
G | A | 1 | a0001c0001t0003g0260 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1734-7566C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794086 | ||||||
chr11:111794181
|
A | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-7661T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794181 | ||||||
chr11:111794681
|
C | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1734-8161G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794681 | ||||||
chr11:111794758
|
G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1734-8238C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794758 | ||||||
chr11:111794956
|
G | A | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1734-8436C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794956 | ||||||
chr11:111795007
|
G | A | 21 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(18): Show | 21 | HG00733.hp2 HG01099.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.1734-8487C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795007 | ||||||
chr11:111795068
|
AAG | A | 8 | a0001c0001t0009g0285a0001c0001t0011g0129a0001c0001t0016g0127others(5): Show | 8 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1734-8550_1734-854 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795068 | ||||||
chr11:111795350
|
G | A | 4 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734-8830C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795350 | ||||||
chr11:111795382
|
G | A | 2 | a0001c0001t0002g0147a0001c0001t0002g0160 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1734-8862C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795382 | ||||||
chr11:111795391
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0006g0142a0001c0001t0006g0143others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734-8871C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795391 | ||||||
chr11:111795404
|
C | T | 230 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(227): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1734-8884G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795404 | ||||||
chr11:111795510
|
G | A | 2 | a0002c0002t0001g0018a0002c0002t0001g0089 | 2 | HG00609.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1734-8990C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795510 | ||||||
chr11:111795548
|
A | C | 1 | a0001c0001t0002g0008 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1734-9028T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795548 | ||||||
chr11:111795686
|
C | T | 2 | a0002c0002t0001g0039a0002c0002t0001g0074 | 2 | HG01109.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1734-9166G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795686 | ||||||
chr11:111795831
|
A | G | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-9311T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795831 | ||||||
chr11:111795945
|
C | T | 1 | a0001c0001t0002g0187 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1734-9425G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795945 | ||||||
chr11:111795992
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1734-9472G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795992 | ||||||
chr11:111796617
|
G | T | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1734-10097C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796617 | ||||||
chr11:111796790
|
G | A | 1 | a0001c0001t0013g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1734-10270C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796790 | ||||||
chr11:111796940
|
T | G | 1 | a0002c0002t0021g0068 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1734-10420A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796940 | ||||||
chr11:111796951
|
C | T | 4 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(1): Show | 4 | NA18977.hp1 NA19054.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734-10431G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796951 | ||||||
chr11:111796965
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1734-10445C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796965 | ||||||
chr11:111797231
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1734-10711A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797231 | ||||||
chr11:111797356
|
C | G | 1 | a0001c0001t0002g0204 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1734-10836G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797356 | ||||||
chr11:111797461
|
T | C | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1734-10941A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797461 | ||||||
chr11:111797463
|
C | T | 1 | a0002c0002t0004g0104 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1734-10943G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797463 | ||||||
chr11:111797498
|
C | T | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0031g0109 | 3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1734-10978G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797498 | ||||||
chr11:111797532
|
A | C | 76 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0210others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1734-11012T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797532 | ||||||
chr11:111797553
|
G | A | 13 | a0001c0001t0005g0005a0001c0001t0005g0111a0001c0001t0005g0114others(10): Show | 14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1734-11033C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797553 | ||||||
chr11:111797751
|
C | T | 2 | a0001c0001t0003g0214a0001c0001t0003g0260 | 2 | NA18968.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1734-11231G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797751 | ||||||
chr11:111797861
|
C | T | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1734-11341G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797861 | ||||||
chr11:111797888
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1734-11368C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797888 | ||||||
chr11:111797888
|
G | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-11368C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797888 | ||||||
chr11:111797895
|
A | T | 209 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0003g0010others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1734-11375T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797895 | ||||||
chr11:111798081
|
C | T | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1734-11561G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798081 | ||||||
chr11:111798152
|
G | C | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+11491C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798152 | ||||||
chr11:111798190
|
G | A | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+11453C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798190 | ||||||
chr11:111798535
|
T | A | 2 | a0001c0001t0001g0212a0002c0002t0001g0031 | 2 | HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1733+11108A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798535 | ||||||
chr11:111798605
|
T | C | 1 | a0001c0001t0002g0204 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1733+11038A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798605 | ||||||
chr11:111798911
|
C | T | 1 | a0002c0002t0004g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1733+10732G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798911 | ||||||
chr11:111799038
|
A | G | 21 | a0001c0001t0001g0014a0001c0001t0005g0005a0001c0001t0005g0111others(18): Show | 22 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1733+10605T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799038 | ||||||
chr11:111799335
|
T | C | 209 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0003g0010others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1733+10308A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799335 | ||||||
chr11:111799358
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0255 | 3 | HG02647.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1733+10285C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799358 | ||||||
chr11:111799436
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1733+10207G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799436 | ||||||
chr11:111799446
|
C | CT | 74 | a0001c0001t0001g0014a0001c0001t0003g0010a0001c0001t0003g0013others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1733+10196dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799446 | ||||||
chr11:111799446
|
CT | C | 29 | a0001c0001t0002g0130a0001c0001t0002g0173a0001c0001t0002g0186others(26): Show | 30 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.1733+10196delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799446 | ||||||
chr11:111799551
|
T | C | 1 | a0001c0001t0003g0258 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1733+10092A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799551 | ||||||
chr11:111799590
|
C | T | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+10053G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799590 | ||||||
chr11:111800134
|
A | C | 97 | a0001c0001t0004g0110a0002c0002t0001g0001a0002c0002t0001g0003others(94): Show | 101 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1733+9509T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800134 | ||||||
chr11:111800256
|
G | A | 99 | a0001c0001t0004g0110a0002c0002t0001g0001a0002c0002t0001g0003others(96): Show | 103 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1733+9387C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800256 | ||||||
chr11:111800296
|
T | C | 79 | a0001c0001t0001g0212a0001c0001t0002g0169a0001c0001t0002g0177others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.1733+9347A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800296 | ||||||
chr11:111800307
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1733+9336A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800307 | ||||||
chr11:111800467
|
C | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0111a0001c0001t0005g0114others(10): Show | 14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1733+9176G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800467 | ||||||
chr11:111800667
|
A | G | 1 | a0001c0001t0003g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1733+8976T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800667 | ||||||
chr11:111800766
|
G | T | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+8877C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800766 | ||||||
chr11:111800819
|
A | G | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+8824T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800819 | ||||||
chr11:111800996
|
T | C | 4 | a0001c0001t0004g0110a0002c0002t0004g0021a0002c0002t0004g0101others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+8647A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800996 | ||||||
chr11:111801001
|
C | T | 13 | a0001c0001t0005g0005a0001c0001t0005g0111a0001c0001t0005g0114others(10): Show | 14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1733+8642G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801001 | ||||||
chr11:111801093
|
T | C | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+8550A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801093 | ||||||
chr11:111801287
|
T | G | 1 | a0002c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1733+8356A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801287 | ||||||
chr11:111801579
|
G | C | 1 | a0001c0001t0003g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1733+8064C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801579 | ||||||
chr11:111801622
|
G | C | 2 | a0002c0002t0021g0011a0002c0002t0021g0068 | 2 | HG00621.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1733+8021C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801622 | ||||||
chr11:111801758
|
C | G | 2 | a0001c0001t0003g0230a0001c0001t0003g0232 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1733+7885G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801758 | ||||||
chr11:111802144
|
C | T | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+7499G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802144 | ||||||
chr11:111802151
|
T | C | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733+7492A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802151 | ||||||
chr11:111802296
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1733+7347T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802296 | ||||||
chr11:111802386
|
C | G | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1733+7257G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802386 | ||||||
chr11:111802476
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1733+7167G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802476 | ||||||
chr11:111802815
|
A | G | 76 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1733+6828T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802815 | ||||||
chr11:111803004
|
G | A | 1 | a0002c0002t0004g0104 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1733+6639C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803004 | ||||||
chr11:111803099
|
T | G | 4 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0005g0298others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733+6544A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803099 | ||||||
chr11:111803110
|
T | C | 1 | a0001c0001t0002g0151 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1733+6533A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803110 | ||||||
chr11:111803198
|
A | C | 7 | a0002c0002t0001g0043a0002c0002t0001g0049a0002c0002t0001g0066others(4): Show | 7 | HG01192.hp1 HG01934.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1733+6445T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803198 | ||||||
chr11:111803334
|
T | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+6309A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803334 | ||||||
chr11:111803503
|
GA | G | 298 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(295): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1733+6139delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803503 | ||||||
chr11:111803562
|
C | T | 1 | a0001c0010t0002g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1733+6081G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803562 | ||||||
chr11:111803729
|
A | G | 3 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0012g0199 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1733+5914T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803729 | ||||||
chr11:111804082
|
AAG | A | 8 | a0001c0001t0009g0285a0001c0001t0011g0129a0001c0001t0016g0127others(5): Show | 8 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1733+5559_1733+556 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804082 | ||||||
chr11:111804132
|
CA | C | 220 | a0001c0001t0001g0212a0001c0001t0001g0287a0001c0001t0001g0291others(217): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1733+5510delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804132 | ||||||
chr11:111804132
|
CAA | C | 9 | a0001c0001t0001g0014a0001c0001t0010g0289a0001c0001t0015g0146others(6): Show | 9 | HG02735.hp1 HG02886.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1733+5509_1733+551 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804132 | ||||||
chr11:111804159
|
C | T | 20 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(17): Show | 20 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1733+5484G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804159 | ||||||
chr11:111804174
|
A | G | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1733+5469T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804174 | ||||||
chr11:111804209
|
A | T | 1 | a0001c0001t0003g0279 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1733+5434T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804209 | ||||||
chr11:111804242
|
T | G | 1 | a0001c0001t0003g0211 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1733+5401A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804242 | ||||||
chr11:111804368
|
A | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1733+5275T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804368 | ||||||
chr11:111804583
|
C | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1733+5060G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804583 | ||||||
chr11:111804901
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1733+4742C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804901 | ||||||
chr11:111804911
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+4732T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804911 | ||||||
chr11:111804932
|
T | C | 1 | a0002c0002t0001g0060 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1733+4711A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804932 | ||||||
chr11:111804950
|
C | T | 4 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0012g0199others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733+4693G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804950 | ||||||
chr11:111805145
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1733+4498T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805145 | ||||||
chr11:111805274
|
G | C | 3 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0074 | 3 | HG01109.hp1 HG03490.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1733+4369C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805274 | ||||||
chr11:111805331
|
G | A | 1 | a0007c0009t0002g0131 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1733+4312C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805331 | ||||||
chr11:111805602
|
A | G | 2 | a0002c0002t0001g0053a0006c0008t0001g0057 | 2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1733+4041T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805602 | ||||||
chr11:111805846
|
G | A | 2 | a0001c0006t0003g0257a0001c0006t0003g0261 | 2 | NA18943.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1733+3797C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805846 | ||||||
chr11:111805905
|
G | C | 1 | a0001c0001t0003g0252 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1733+3738C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805905 | ||||||
chr11:111806150
|
G | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1733+3493C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806150 | ||||||
chr11:111806328
|
T | G | 3 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0012g0199 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1733+3315A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806328 | ||||||
chr11:111806345
|
C | T | 1 | a0001c0001t0003g0236 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1733+3298G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806345 | ||||||
chr11:111806393
|
T | A | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+3250A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806393 | ||||||
chr11:111806401
|
G | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+3242C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806401 | ||||||
chr11:111806496
|
G | C | 1 | a0001c0001t0002g0130 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1733+3147C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806496 | ||||||
chr11:111806543
|
C | T | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+3100G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806543 | ||||||
chr11:111806971
|
A | T | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1733+2672T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806971 | ||||||
chr11:111806973
|
A | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+2670T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806973 | ||||||
chr11:111807258
|
T | A | 98 | a0001c0001t0004g0110a0002c0002t0001g0001a0002c0002t0001g0003others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1733+2385A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807258 | ||||||
chr11:111807661
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1733+1982C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807661 | ||||||
chr11:111807698
|
A | AGGTG | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+1941_1733+194 others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807698 | ||||||
chr11:111807734
|
G | A | 1 | a0004c0004t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1733+1909C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807734 | ||||||
chr11:111807777
|
C | T | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+1866G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807777 | ||||||
chr11:111807800
|
A | T | 131 | a0001c0001t0001g0014a0001c0001t0002g0209a0001c0001t0004g0110others(128): Show | 136 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1733+1843T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807800 | ||||||
chr11:111808023
|
T | C | 1 | a0002c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1733+1620A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808023 | ||||||
chr11:111808047
|
T | C | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1733+1596A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808047 | ||||||
chr11:111808538
|
C | T | 76 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1733+1105G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808538 | ||||||
chr11:111808634
|
G | A | 1 | a0001c0001t0019g0220 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1733+1009C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808634 | ||||||
chr11:111808645
|
T | C | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1733+998A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808645 | ||||||
chr11:111808791
|
C | G | 1 | a0004c0004t0001g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1733+852G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808791 | ||||||
chr11:111808845
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1733+798G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808845 | ||||||
chr11:111808850
|
A | T | 6 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0018others(3): Show | 6 | HG00609.hp2 NA18946.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.1733+793T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808850 | ||||||
chr11:111808907
|
C | G | 1 | a0001c0001t0003g0222 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1733+736G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808907 | ||||||
chr11:111809050
|
C | T | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+593G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809050 | ||||||
chr11:111809223
|
G | T | 1 | a0001c0001t0002g0008 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1733+420C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809223 | ||||||
chr11:111809229
|
A | G | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1733+414T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809229 | ||||||
chr11:111809251
|
G | A | 9 | a0001c0001t0002g0180a0001c0001t0009g0285a0001c0001t0011g0129others(6): Show | 9 | HG01952.hp1 HG02145.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.1733+392C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809251 | ||||||
chr11:111809403
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1733+240C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809403 | ||||||
chr11:111809407
|
G | A | 1 | a0001c0001t0003g0238 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1733+236C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809407 | ||||||
chr11:111809517
|
T | TAC | 14 | a0001c0001t0002g0159a0001c0001t0003g0267a0001c0001t0010g0288others(11): Show | 14 | HG01515.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1733+124_1733+125d others(4): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | ||||||
chr11:111809517
|
T | TACAC | 113 | a0001c0001t0001g0014a0001c0001t0004g0110a0001c0001t0005g0005others(110): Show | 118 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.1733+122_1733+125d others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | ||||||
chr11:111809517
|
T | TACACAC | 7 | a0001c0001t0005g0118a0001c0001t0005g0121a0002c0002t0001g0031others(4): Show | 7 | HG00597.hp1 HG00738.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1733+120_1733+125d others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | ||||||
chr11:111809517
|
T | TACACACA others(3): Show |
1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+116_1733+125d others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | ||||||
chr11:111809517
|
T | TACACACA others(5): Show |
2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+114_1733+125d others(14): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | ||||||
chr11:111809605
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1733+38G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809605 | ||||||
chr11:111809899
|
T | C | 1 | a0002c0002t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1603-126A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111809899 | ||||||
chr11:111809909
|
G | A | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-136C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111809909 | ||||||
chr11:111809962
|
C | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-189G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111809962 | ||||||
chr11:111810181
|
C | T | 3 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0012g0199 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-408G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810181 | ||||||
chr11:111810282
|
T | C | 1 | a0001c0001t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1603-509A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810282 | ||||||
chr11:111810320
|
G | C | 1 | a0002c0002t0001g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1603-547C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810320 | ||||||
chr11:111810370
|
T | A | 3 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0012g0199 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-597A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810370 | ||||||
chr11:111810376
|
C | G | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-603G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810376 | ||||||
chr11:111810544
|
C | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-771G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810544 | ||||||
chr11:111811323
|
A | G | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603-1550T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811323 | ||||||
chr11:111811440
|
G | A | 4 | a0002c0002t0001g0050a0002c0002t0001g0063a0002c0002t0001g0070others(1): Show | 4 | NA18939.hp1 NA18955.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-1667C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811440 | ||||||
chr11:111811480
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1603-1707A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811480 | ||||||
chr11:111811542
|
C | CA | 11 | a0001c0001t0002g0130a0001c0001t0002g0202a0001c0001t0005g0119others(8): Show | 11 | HG01109.hp1 HG01952.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1603-1770dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811542 | ||||||
chr11:111811542
|
CA | C | 103 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0003g0010others(100): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.1603-1770delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811542 | ||||||
chr11:111811597
|
T | C | 2 | a0001c0001t0003g0262a0001c0001t0003g0277 | 2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1603-1824A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811597 | ||||||
chr11:111811603
|
CATGTGGT others(17): Show |
C | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1603-1854_1603-183 others(28): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811603 | ||||||
chr11:111811644
|
C | T | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-1871G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811644 | ||||||
chr11:111811747
|
A | G | 3 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0012g0199 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-1974T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811747 | ||||||
chr11:111811886
|
A | G | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-2113T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811886 | ||||||
chr11:111812129
|
T | A | 3 | a0001c0001t0003g0246a0001c0001t0003g0247a0001c0001t0003g0265 | 3 | HG01069.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1603-2356A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812129 | ||||||
chr11:111812267
|
T | C | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1603-2494A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812267 | ||||||
chr11:111812418
|
T | C | 76 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1603-2645A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812418 | ||||||
chr11:111812670
|
ACTTTGGG others(14): Show |
A | 1 | a0001c0001t0003g0237 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1603-2918_1603-289 others(25): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812670 | ||||||
chr11:111812842
|
C | T | 1 | a0002c0002t0001g0019 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1603-3069G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812842 | ||||||
chr11:111812852
|
G | A | 3 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0012g0199 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-3079C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812852 | ||||||
chr11:111812867
|
A | G | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-3094T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812867 | ||||||
chr11:111812899
|
G | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-3126C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812899 | ||||||
chr11:111812915
|
C | CAAAAA | 7 | a0001c0001t0008g0264a0001c0001t0012g0197a0001c0001t0020g0108others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-3147_1603-314 others(9): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | ||||||
chr11:111812915
|
C | CAAAAAA | 88 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0002g0178others(85): Show | 90 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1603-3148_1603-314 others(10): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | ||||||
chr11:111812915
|
C | CAAAAAAA | 69 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.1603-3149_1603-314 others(11): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | ||||||
chr11:111812915
|
C | CAAAAAAA others(1): Show |
13 | a0001c0001t0001g0294a0001c0001t0002g0149a0001c0001t0002g0151others(10): Show | 13 | HG00733.hp2 HG01099.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1603-3150_1603-314 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | ||||||
chr11:111812915
|
C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(9): Show | 12 | HG02723.hp1 HG02895.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603-3151_1603-314 others(13): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | ||||||
chr11:111812915
|
CAAAAAA | C | 99 | a0001c0001t0004g0110a0002c0002t0001g0001a0002c0002t0001g0003others(96): Show | 103 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1603-3148_1603-314 others(10): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | ||||||
chr11:111813049
|
C | CG | 301 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(298): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1603-3277dupC | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813049 | ||||||
chr11:111813072
|
G | GCT | 301 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(298): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1603-3300_1603-329 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813072 | ||||||
chr11:111813073
|
T | A | 301 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(298): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1603-3300A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813073 | ||||||
chr11:111813179
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1603-3406G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813179 | ||||||
chr11:111813184
|
G | A | 3 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0005g0299 | 3 | HG02723.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1603-3411C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813184 | ||||||
chr11:111813251
|
T | C | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0190 | 3 | HG01261.hp2 HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1603-3478A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813251 | ||||||
chr11:111813289
|
T | G | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-3516A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813289 | ||||||
chr11:111813353
|
G | A | 10 | a0002c0002t0001g0015a0002c0002t0001g0028a0002c0002t0001g0029others(7): Show | 10 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603-3580C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813353 | ||||||
chr11:111813515
|
C | T | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1603-3742G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813515 | ||||||
chr11:111813644
|
T | C | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-3871A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813644 | ||||||
chr11:111813675
|
C | A | 1 | a0001c0001t0005g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1603-3902G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813675 | ||||||
chr11:111813748
|
C | G | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-3975G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813748 | ||||||
chr11:111814129
|
A | G | 4 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0005g0298others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-4356T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814129 | ||||||
chr11:111814535
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1603-4762C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814535 | ||||||
chr11:111814685
|
A | G | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-4912T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814685 | ||||||
chr11:111814693
|
A | G | 1 | a0002c0002t0004g0036 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1603-4920T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814693 | ||||||
chr11:111814746
|
T | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-4973A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814746 | ||||||
chr11:111815096
|
G | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0277 | 2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1603-5323C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815096 | ||||||
chr11:111815158
|
G | A | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-5385C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815158 | ||||||
chr11:111815267
|
T | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-5494A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815267 | ||||||
chr11:111815289
|
T | C | 4 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-5516A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815289 | ||||||
chr11:111815303
|
T | A | 1 | a0001c0001t0002g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1603-5530A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815303 | ||||||
chr11:111815313
|
G | A | 1 | a0002c0002t0002g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1603-5540C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815313 | ||||||
chr11:111815367
|
C | T | 3 | a0001c0001t0003g0238a0001c0001t0003g0267a0001c0001t0008g0264 | 3 | NA18939.hp2 NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1603-5594G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815367 | ||||||
chr11:111815667
|
G | GT | 3 | a0001c0001t0007g0231a0001c0001t0007g0244a0001c0001t0007g0263 | 3 | HG01891.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1603-5895_1603-589 others(5): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815667 | ||||||
chr11:111815668
|
A | T | 3 | a0001c0001t0007g0231a0001c0001t0007g0244a0001c0001t0007g0263 | 3 | HG01891.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1603-5895T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815668 | ||||||
chr11:111815686
|
T | C | 3 | a0001c0001t0002g0161a0001c0001t0002g0167a0001c0001t0002g0193 | 3 | HG01256.hp1 HG01258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1603-5913A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815686 | ||||||
chr11:111815858
|
G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1603-6085C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815858 | ||||||
chr11:111815941
|
T | C | 1 | a0001c0001t0003g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1603-6168A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815941 | ||||||
chr11:111816011
|
A | T | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-6238T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816011 | ||||||
chr11:111816076
|
C | T | 230 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(227): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1603-6303G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816076 | ||||||
chr11:111816139
|
T | C | 1 | a0002c0002t0001g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1603-6366A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816139 | ||||||
chr11:111816318
|
T | C | 1 | a0002c0002t0004g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1603-6545A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816318 | ||||||
chr11:111816677
|
T | C | 1 | a0001c0001t0003g0235 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1603-6904A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816677 | ||||||
chr11:111816733
|
T | G | 3 | a0001c0001t0002g0161a0001c0001t0002g0167a0001c0001t0002g0193 | 3 | HG01256.hp1 HG01258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1603-6960A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816733 | ||||||
chr11:111816745
|
A | G | 1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1603-6972T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816745 | ||||||
chr11:111817034
|
A | G | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-7261T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817034 | ||||||
chr11:111817268
|
G | A | 1 | a0001c0001t0002g0162 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1603-7495C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817268 | ||||||
chr11:111817411
|
T | C | 5 | a0001c0001t0011g0129a0001c0001t0016g0127a0001c0001t0016g0128others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-7638A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817411 | ||||||
chr11:111817563
|
C | T | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-7790G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817563 | ||||||
chr11:111817603
|
C | A | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-7830G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817603 | ||||||
chr11:111817777
|
C | CT | 9 | a0001c0001t0002g0164a0001c0001t0003g0010a0001c0001t0003g0255others(6): Show | 10 | HG00733.hp2 HG01099.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603-8005dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817777 | ||||||
chr11:111817777
|
CT | C | 8 | a0001c0001t0002g0158a0001c0001t0002g0163a0003c0003t0001g0123others(5): Show | 8 | HG01884.hp1 HG01975.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603-8005delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817777 | ||||||
chr11:111817782
|
T | C | 3 | a0002c0002t0001g0071a0002c0002t0001g0080a0002c0002t0030g0082 | 3 | HG02602.hp2 HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1603-8009A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817782 | ||||||
chr11:111817784
|
T | C | 1 | a0001c0001t0007g0263 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1603-8011A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817784 | ||||||
chr11:111817865
|
C | T | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603-8092G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817865 | ||||||
chr11:111817868
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1603-8095C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817868 | ||||||
chr11:111818022
|
G | A | 1 | a0007c0009t0002g0131 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1603-8249C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818022 | ||||||
chr11:111818158
|
G | A | 3 | a0001c0001t0010g0288a0001c0001t0010g0289a0001c0001t0010g0290 | 3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1603-8385C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818158 | ||||||
chr11:111818273
|
A | G | 2 | a0001c0001t0003g0249a0001c0001t0003g0250 | 2 | HG02004.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1603-8500T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818273 | ||||||
chr11:111818455
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1603-8682C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818455 | ||||||
chr11:111818525
|
C | T | 2 | a0001c0001t0002g0135a0001c0001t0002g0202 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1603-8752G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818525 | ||||||
chr11:111818597
|
A | C | 1 | a0001c0001t0003g0249 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1603-8824T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818597 | ||||||
chr11:111818623
|
C | T | 3 | a0001c0001t0010g0288a0001c0001t0010g0289a0001c0001t0010g0290 | 3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1603-8850G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818623 | ||||||
chr11:111818692
|
T | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-8919A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818692 | ||||||
chr11:111818812
|
C | G | 1 | a0001c0001t0003g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1603-9039G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818812 | ||||||
chr11:111818871
|
A | G | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-9098T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818871 | ||||||
chr11:111819118
|
G | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-9345C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819118 | ||||||
chr11:111819293
|
A | G | 12 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(9): Show | 12 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603-9520T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819293 | ||||||
chr11:111819298
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1603-9525A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819298 | ||||||
chr11:111819348
|
G | T | 3 | a0002c0002t0001g0028a0002c0002t0001g0067a0002c0002t0001g0088 | 3 | NA18941.hp1 NA18979.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1603-9575C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819348 | ||||||
chr11:111819399
|
C | T | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-9626G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819399 | ||||||
chr11:111819460
|
T | C | 11 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(8): Show | 11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1603-9687A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819460 | ||||||
chr11:111819607
|
A | G | 209 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1603-9834T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819607 | ||||||
chr11:111819804
|
G | C | 2 | a0002c0002t0001g0018a0002c0002t0001g0089 | 2 | HG00609.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1603-10031C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819804 | ||||||
chr11:111819806
|
A | G | 2 | a0001c0001t0002g0201a0001c0001t0025g0133 | 2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1603-10033T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819806 | ||||||
chr11:111819858
|
T | G | 1 | a0001c0001t0002g0171 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1603-10085A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819858 | ||||||
chr11:111819863
|
G | A | 13 | a0001c0001t0005g0005a0001c0001t0005g0111a0001c0001t0005g0114others(10): Show | 14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1603-10090C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819863 | ||||||
chr11:111819899
|
G | C | 1 | a0001c0001t0003g0240 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1603-10126C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819899 | ||||||
chr11:111819952
|
A | G | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0031g0109 | 3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1603-10179T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819952 | ||||||
chr11:111820088
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1603-10315C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820088 | ||||||
chr11:111820407
|
C | A | 4 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-10634G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820407 | ||||||
chr11:111820579
|
G | C | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-10806C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820579 | ||||||
chr11:111820736
|
G | A | 3 | a0002c0002t0001g0052a0002c0002t0001g0056a0002c0002t0001g0091 | 3 | HG02698.hp1 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1603-10963C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820736 | ||||||
chr11:111820755
|
C | T | 4 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-10982G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820755 | ||||||
chr11:111820867
|
A | AG | 301 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(298): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1603-11095dupC | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820867 | ||||||
chr11:111820920
|
G | GCA | 19 | a0001c0001t0001g0014a0001c0001t0006g0142a0001c0001t0006g0144others(16): Show | 19 | HG01952.hp1 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1603-11149_1603-11 others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | ||||||
chr11:111820920
|
G | GCACA | 81 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.1603-11151_1603-11 others(10): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | ||||||
chr11:111820920
|
G | GCACACA | 7 | a0001c0001t0003g0239a0001c0001t0003g0282a0001c0001t0005g0005others(4): Show | 8 | HG00597.hp2 HG00642.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603-11153_1603-11 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | ||||||
chr11:111820920
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-11157_1603-11 others(16): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | ||||||
chr11:111820920
|
G | GCGCACA | 7 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0116others(4): Show | 7 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-11148_1603-11 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | ||||||
chr11:111820920
|
GCA | G | 93 | a0001c0001t0002g0158a0001c0001t0002g0162a0001c0001t0002g0187others(90): Show | 97 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1603-11149_1603-11 others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | ||||||
chr11:111820920
|
GCACACA | G | 4 | a0004c0004t0001g0096a0004c0004t0001g0097a0004c0004t0001g0098others(1): Show | 4 | HG00597.hp1 NA18968.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-11153_1603-11 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | ||||||
chr11:111820920
|
GCACACAC others(5): Show |
G | 2 | a0002c0002t0004g0025a0002c0002t0004g0026 | 2 | NA18956.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1603-11159_1603-11 others(18): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | ||||||
chr11:111821036
|
C | T | 1 | a0002c0002t0001g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1603-11263G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821036 | ||||||
chr11:111821143
|
C | T | 3 | a0001c0001t0010g0288a0001c0001t0010g0289a0001c0001t0010g0290 | 3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1603-11370G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821143 | ||||||
chr11:111821243
|
C | T | 6 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603-11470G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821243 | ||||||
chr11:111821249
|
G | A | 1 | a0001c0001t0018g0301 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1603-11476C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821249 | ||||||
chr11:111821295
|
C | G | 6 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0018others(3): Show | 6 | HG00609.hp2 NA18946.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-11522G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821295 | ||||||
chr11:111821458
|
G | A | 76 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1603-11685C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821458 | ||||||
chr11:111821781
|
G | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-12008C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821781 | ||||||
chr11:111821893
|
G | C | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-12120C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821893 | ||||||
chr11:111821925
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1603-12152G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821925 | ||||||
chr11:111821940
|
G | C | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-12167C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821940 | ||||||
chr11:111822099
|
G | T | 2 | a0002c0002t0001g0058a0002c0002t0001g0060 | 2 | HG00544.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1603-12326C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822099 | ||||||
chr11:111822100
|
A | T | 2 | a0002c0002t0001g0058a0002c0002t0001g0060 | 2 | HG00544.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1603-12327T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822100 | ||||||
chr11:111822146
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0009g0285a0001c0001t0011g0129others(6): Show | 9 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1603-12373G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822146 | ||||||
chr11:111822232
|
AC | A | 301 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(298): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1603-12460delG | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822232 | ||||||
chr11:111822275
|
G | A | 1 | a0001c0001t0008g0216 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1603-12502C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822275 | ||||||
chr11:111822310
|
G | C | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-12537C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822310 | ||||||
chr11:111822408
|
C | CA | 244 | a0001c0001t0001g0212a0001c0001t0001g0293a0001c0001t0002g0002others(241): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1603-12636dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822408 | ||||||
chr11:111822408
|
C | CAA | 32 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0294others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1603-12637_1603-12 others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822408 | ||||||
chr11:111822408
|
C | CAAA | 7 | a0001c0001t0003g0274a0001c0001t0005g0296a0001c0001t0005g0297others(4): Show | 7 | HG02723.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-12638_1603-12 others(9): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822408 | ||||||
chr11:111822493
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1603-12720G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822493 | ||||||
chr11:111822538
|
C | T | 2 | a0002c0002t0001g0072a0002c0002t0001g0073 | 2 | NA18612.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1603-12765G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822538 | ||||||
chr11:111822558
|
A | G | 1 | a0001c0001t0003g0233 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1603-12785T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822558 | ||||||
chr11:111822613
|
C | A | 1 | a0002c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1603-12840G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822613 | ||||||
chr11:111822677
|
C | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-12904G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822677 | ||||||
chr11:111822730
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-12957G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822730 | ||||||
chr11:111822930
|
G | A | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1603-13157C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822930 | ||||||
chr11:111822949
|
G | A | 1 | a0002c0002t0001g0055 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1603-13176C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822949 | ||||||
chr11:111823074
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1602+13091C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823074 | ||||||
chr11:111823139
|
T | C | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1602+13026A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823139 | ||||||
chr11:111823433
|
C | G | 7 | a0002c0002t0002g0023a0002c0002t0004g0021a0002c0002t0004g0086others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+12732G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823433 | ||||||
chr11:111823479
|
A | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+12686T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823479 | ||||||
chr11:111823590
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1602+12575A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823590 | ||||||
chr11:111823668
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1602+12497C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823668 | ||||||
chr11:111823766
|
T | C | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1602+12399A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823766 | ||||||
chr11:111823788
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1602+12377A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823788 | ||||||
chr11:111824111
|
G | A | 2 | a0001c0001t0020g0107a0001c0001t0020g0108 | 2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1602+12054C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824111 | ||||||
chr11:111824164
|
G | A | 2 | a0002c0002t0001g0053a0006c0008t0001g0057 | 2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1602+12001C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824164 | ||||||
chr11:111824243
|
C | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+11922G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824243 | ||||||
chr11:111824306
|
G | GA | 86 | a0001c0001t0003g0237a0002c0002t0001g0001a0002c0002t0001g0003others(83): Show | 90 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1602+11858dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824306 | ||||||
chr11:111824360
|
T | C | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1602+11805A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824360 | ||||||
chr11:111824693
|
T | C | 13 | a0001c0001t0005g0005a0001c0001t0005g0111a0001c0001t0005g0114others(10): Show | 14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1602+11472A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824693 | ||||||
chr11:111824985
|
C | T | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1602+11180G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824985 | ||||||
chr11:111825011
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1602+11154C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825011 | ||||||
chr11:111825120
|
A | C | 6 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+11045T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825120 | ||||||
chr11:111825489
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1602+10676T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825489 | ||||||
chr11:111825519
|
T | C | 4 | a0004c0004t0001g0096a0004c0004t0001g0097a0004c0004t0001g0098others(1): Show | 4 | HG00597.hp1 NA18968.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+10646A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825519 | ||||||
chr11:111825570
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1602+10595G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825570 | ||||||
chr11:111825692
|
T | C | 15 | a0001c0001t0005g0005a0001c0001t0005g0111a0001c0001t0005g0114others(12): Show | 16 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+10473A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825692 | ||||||
chr11:111825716
|
T | C | 204 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(201): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1602+10449A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825716 | ||||||
chr11:111825775
|
C | T | 1 | a0005c0007t0009g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1602+10390G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825775 | ||||||
chr11:111826021
|
G | A | 1 | a0001c0001t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1602+10144C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826021 | ||||||
chr11:111826066
|
C | CAAT | 3 | a0001c0001t0002g0135a0001c0001t0002g0202a0002c0002t0004g0054 | 3 | HG02055.hp2 HG03098.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1602+10096_1602+10 others(9): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | ||||||
chr11:111826066
|
C | CAATAAT | 130 | a0001c0001t0001g0212a0001c0001t0002g0002a0001c0001t0002g0006others(127): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1602+10093_1602+10 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | ||||||
chr11:111826066
|
C | CAATAATA others(2): Show |
25 | a0001c0001t0002g0157a0001c0001t0002g0184a0001c0001t0003g0222others(22): Show | 26 | HG00408.hp2 HG00733.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1602+10090_1602+10 others(15): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | ||||||
chr11:111826066
|
C | CAATAATA others(5): Show |
93 | a0001c0001t0001g0014a0001c0001t0001g0293a0001c0001t0002g0130others(90): Show | 96 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1602+10087_1602+10 others(18): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | ||||||
chr11:111826066
|
C | CAATAATA others(8): Show |
43 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0294others(40): Show | 43 | HG01884.hp1 HG01952.hp1 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1602+10084_1602+10 others(21): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | ||||||
chr11:111826066
|
C | CAATAATA others(11): Show |
4 | a0001c0001t0003g0240a0001c0001t0005g0296a0002c0002t0004g0026others(1): Show | 4 | HG03098.hp2 HG04204.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+10081_1602+10 others(24): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | ||||||
chr11:111826391
|
TA | T | 210 | a0001c0001t0001g0212a0001c0001t0001g0287a0001c0001t0001g0291others(207): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1602+9773delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826391 | ||||||
chr11:111826393
|
A | T | 1 | a0001c0001t0003g0292 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1602+9772T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826393 | ||||||
chr11:111826401
|
A | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+9764T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826401 | ||||||
chr11:111826407
|
A | C | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1602+9758T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826407 | ||||||
chr11:111826518
|
G | A | 6 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+9647C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826518 | ||||||
chr11:111826549
|
C | T | 1 | a0001c0001t0025g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1602+9616G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826549 | ||||||
chr11:111826639
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1602+9526T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826639 | ||||||
chr11:111826849
|
G | A | 3 | a0001c0001t0010g0288a0001c0001t0010g0289a0001c0001t0010g0290 | 3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1602+9316C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826849 | ||||||
chr11:111826980
|
T | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+9185A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826980 | ||||||
chr11:111827353
|
G | C | 1 | a0001c0001t0002g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1602+8812C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827353 | ||||||
chr11:111827435
|
A | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+8730T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827435 | ||||||
chr11:111827492
|
CAT | C | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1602+8671_1602+867 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827492 | ||||||
chr11:111827604
|
C | T | 1 | a0001c0001t0012g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1602+8561G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827604 | ||||||
chr11:111827605
|
G | A | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+8560C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827605 | ||||||
chr11:111827673
|
G | C | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1602+8492C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827673 | ||||||
chr11:111827781
|
C | A | 5 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+8384G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827781 | ||||||
chr11:111827867
|
C | CA | 7 | a0001c0001t0002g0156a0001c0001t0002g0176a0001c0001t0003g0252others(4): Show | 7 | HG00544.hp1 HG02155.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+8297dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827867 | ||||||
chr11:111827913
|
C | T | 1 | a0001c0001t0002g0009 | 2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1602+8252G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827913 | ||||||
chr11:111827914
|
G | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+8251C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827914 | ||||||
chr11:111827974
|
C | G | 6 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+8191G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827974 | ||||||
chr11:111828087
|
A | G | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1602+8078T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828087 | ||||||
chr11:111828116
|
C | A | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1602+8049G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828116 | ||||||
chr11:111828147
|
T | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+8018A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828147 | ||||||
chr11:111828185
|
C | A | 11 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(8): Show | 11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1602+7980G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828185 | ||||||
chr11:111828206
|
T | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1602+7959A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828206 | ||||||
chr11:111828216
|
T | C | 1 | a0002c0002t0004g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1602+7949A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828216 | ||||||
chr11:111828290
|
G | T | 5 | a0001c0001t0002g0156a0001c0001t0002g0163a0001c0001t0002g0180others(2): Show | 5 | HG01975.hp2 HG01993.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+7875C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828290 | ||||||
chr11:111828310
|
C | T | 1 | a0001c0001t0002g0006 | 2 | HG00639.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1602+7855G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828310 | ||||||
chr11:111828448
|
T | C | 1 | a0004c0004t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1602+7717A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828448 | ||||||
chr11:111828500
|
C | T | 76 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1602+7665G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828500 | ||||||
chr11:111828817
|
C | T | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1602+7348G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828817 | ||||||
chr11:111828955
|
T | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+7210A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828955 | ||||||
chr11:111829034
|
A | G | 1 | a0001c0001t0019g0243 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1602+7131T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829034 | ||||||
chr11:111829370
|
G | C | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1602+6795C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829370 | ||||||
chr11:111829493
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1602+6672C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829493 | ||||||
chr11:111829497
|
G | A | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+6668C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829497 | ||||||
chr11:111829508
|
A | C | 1 | a0001c0001t0002g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1602+6657T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829508 | ||||||
chr11:111829575
|
T | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+6590A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829575 | ||||||
chr11:111829586
|
C | T | 1 | a0002c0002t0004g0075 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1602+6579G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829586 | ||||||
chr11:111829651
|
A | C | 5 | a0001c0001t0002g0156a0001c0001t0002g0163a0001c0001t0002g0180others(2): Show | 5 | HG01975.hp2 HG01993.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+6514T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829651 | ||||||
chr11:111829742
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1602+6423C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829742 | ||||||
chr11:111829902
|
T | C | 4 | a0001c0001t0004g0110a0001c0001t0005g0116a0001c0001t0005g0117others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+6263A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829902 | ||||||
chr11:111829913
|
G | C | 1 | a0001c0001t0003g0240 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1602+6252C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829913 | ||||||
chr11:111830072
|
T | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+6093A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830072 | ||||||
chr11:111830371
|
T | C | 11 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(8): Show | 11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1602+5794A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830371 | ||||||
chr11:111830438
|
C | G | 4 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+5727G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830438 | ||||||
chr11:111830546
|
G | A | 204 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(201): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1602+5619C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830546 | ||||||
chr11:111830560
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0011g0129a0001c0001t0016g0127others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+5605T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830560 | ||||||
chr11:111830996
|
C | G | 1 | a0002c0002t0001g0004 | 2 | NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1602+5169G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830996 | ||||||
chr11:111831109
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1602+5056G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831109 | ||||||
chr11:111831126
|
C | T | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+5039G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831126 | ||||||
chr11:111831130
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1602+5035A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831130 | ||||||
chr11:111831229
|
C | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0287a0001c0001t0001g0291others(20): Show | 23 | HG00733.hp2 HG01099.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1602+4936G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831229 | ||||||
chr11:111831233
|
G | A | 2 | a0001c0001t0003g0253a0001c0001t0008g0228 | 2 | NA18985.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1602+4932C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831233 | ||||||
chr11:111831470
|
C | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+4695G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831470 | ||||||
chr11:111831521
|
A | G | 1 | a0001c0001t0023g0269 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1602+4644T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831521 | ||||||
chr11:111831652
|
A | C | 14 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(11): Show | 15 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1602+4513T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831652 | ||||||
chr11:111832446
|
A | AT | 9 | a0001c0001t0001g0014a0001c0001t0009g0285a0001c0001t0011g0129others(6): Show | 9 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1602+3718dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832446 | ||||||
chr11:111832468
|
T | A | 1 | a0001c0001t0002g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1602+3697A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832468 | ||||||
chr11:111832468
|
T | G | 295 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1602+3697A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832468 | ||||||
chr11:111832636
|
T | C | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1602+3529A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832636 | ||||||
chr11:111832796
|
A | G | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1602+3369T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832796 | ||||||
chr11:111832822
|
G | A | 1 | a0002c0002t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1602+3343C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832822 | ||||||
chr11:111832889
|
G | A | 1 | a0001c0005t0011g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1602+3276C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832889 | ||||||
chr11:111833181
|
T | C | 1 | a0001c0001t0023g0269 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1602+2984A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833181 | ||||||
chr11:111833183
|
T | C | 1 | a0001c0001t0002g0177 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+2982A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833183 | ||||||
chr11:111833216
|
C | T | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+2949G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833216 | ||||||
chr11:111833385
|
T | C | 1 | a0001c0001t0002g0204 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1602+2780A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833385 | ||||||
chr11:111833704
|
C | T | 1 | a0002c0002t0001g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1602+2461G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833704 | ||||||
chr11:111834086
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1602+2079G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834086 | ||||||
chr11:111834303
|
G | A | 1 | a0001c0001t0003g0254 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1602+1862C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834303 | ||||||
chr11:111834350
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1602+1815T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834350 | ||||||
chr11:111834404
|
T | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0202 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1602+1761A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834404 | ||||||
chr11:111834455
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1602+1710C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834455 | ||||||
chr11:111834596
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1602+1569T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834596 | ||||||
chr11:111834771
|
G | A | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+1394C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834771 | ||||||
chr11:111835075
|
AGATGTGG others(11): Show |
A | 21 | a0001c0001t0001g0014a0001c0001t0001g0287a0001c0001t0001g0291others(18): Show | 21 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602+1072_1602+108 others(22): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835075 | ||||||
chr11:111835094
|
C | A | 21 | a0001c0001t0001g0014a0001c0001t0001g0287a0001c0001t0001g0291others(18): Show | 21 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602+1071G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835094 | ||||||
chr11:111835382
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1602+783C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835382 | ||||||
chr11:111835388
|
G | T | 59 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(56): Show | 63 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1602+777C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835388 | ||||||
chr11:111835442
|
T | A | 6 | a0001c0001t0001g0014a0001c0001t0011g0129a0001c0001t0016g0127others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+723A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835442 | ||||||
chr11:111835759
|
G | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0160 | 2 | HG00741.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1602+406C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835759 | ||||||
chr11:111835812
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0255 | 3 | HG02647.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1602+353C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835812 | ||||||
chr11:111835830
|
A | G | 1 | a0001c0001t0003g0271 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1602+335T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835830 | ||||||
chr11:111836044
|
C | T | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+121G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111836044 | ||||||
chr11:111836308
|
A | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1473-14T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836308 | ||||||
chr11:111836493
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1473-199A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836493 | ||||||
chr11:111836584
|
T | C | 1 | a0002c0002t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1473-290A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836584 | ||||||
chr11:111836663
|
T | C | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1473-369A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836663 | ||||||
chr11:111836731
|
T | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473-437A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836731 | ||||||
chr11:111836888
|
C | T | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1472+580G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836888 | ||||||
chr11:111837074
|
T | C | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1472+394A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111837074 | ||||||
chr11:111837672
|
T | A | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1325-57A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 11/14 | chr11 | 111837672 | ||||||
chr11:111837673
|
A | T | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1325-58T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 11/14 | chr11 | 111837673 | ||||||
chr11:111837858
|
T | G | 19 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(16): Show | 20 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1325-243A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 11/14 | chr11 | 111837858 | ||||||
chr11:111837945
|
T | A | 207 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(204): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1324+304A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 11/14 | chr11 | 111837945 | ||||||
chr11:111838459
|
C | A | 1 | a0002c0002t0002g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1174-60G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838459 | ||||||
chr11:111838490
|
G | A | 2 | a0001c0001t0005g0118a0001c0001t0005g0121 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1174-91C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838490 | ||||||
chr11:111838524
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1174-125G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838524 | ||||||
chr11:111838591
|
G | A | 2 | a0001c0001t0020g0107a0001c0001t0020g0108 | 2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1174-192C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838591 | ||||||
chr11:111838709
|
A | G | 2 | a0001c0001t0002g0009a0001c0001t0002g0195 | 3 | HG01255.hp2 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1174-310T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838709 | ||||||
chr11:111839049
|
AT | A | 6 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-651delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839049 | ||||||
chr11:111839066
|
C | T | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1174-667G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839066 | ||||||
chr11:111839299
|
A | G | 1 | a0001c0001t0003g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1174-900T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839299 | ||||||
chr11:111839311
|
T | C | 230 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(227): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1174-912A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839311 | ||||||
chr11:111839340
|
C | T | 1 | a0001c0001t0020g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1174-941G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839340 | ||||||
chr11:111839356
|
C | T | 11 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0020g0107others(8): Show | 11 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-957G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839356 | ||||||
chr11:111839376
|
G | A | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1174-977C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839376 | ||||||
chr11:111839414
|
G | A | 1 | a0001c0001t0003g0256 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1174-1015C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839414 | ||||||
chr11:111839584
|
G | A | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1173+1071C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839584 | ||||||
chr11:111839588
|
CA | C | 20 | a0001c0001t0003g0241a0001c0001t0004g0110a0001c0001t0005g0005others(17): Show | 21 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1173+1066delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839588 | ||||||
chr11:111839601
|
A | AG | 25 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(22): Show | 25 | HG00597.hp2 HG00642.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1173+1053dupC | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839601 | ||||||
chr11:111839601
|
AG | A | 66 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(63): Show | 70 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1173+1053delC | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839601 | ||||||
chr11:111839603
|
G | A | 1 | a0002c0002t0001g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1173+1052C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839603 | ||||||
chr11:111839605
|
G | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1173+1050C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839605 | ||||||
chr11:111839826
|
T | G | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1173+829A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839826 | ||||||
chr11:111839907
|
C | A | 1 | a0001c0001t0003g0230 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1173+748G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839907 | ||||||
chr11:111840070
|
G | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1173+585C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111840070 | ||||||
chr11:111840202
|
G | C | 3 | a0001c0001t0003g0258a0001c0006t0003g0257a0001c0006t0003g0261 | 3 | NA18943.hp1 NA19000.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1173+453C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111840202 | ||||||
chr11:111840489
|
C | G | 1 | a0002c0002t0004g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1173+166G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111840489 | ||||||
chr11:111840943
|
C | T | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1019-134G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111840943 | ||||||
chr11:111840958
|
G | A | 1 | a0002c0002t0004g0075 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1019-149C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111840958 | ||||||
chr11:111841216
|
A | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1019-407T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841216 | ||||||
chr11:111841434
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1019-625G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841434 | ||||||
chr11:111841529
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1019-720C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841529 | ||||||
chr11:111841677
|
C | T | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1019-868G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841677 | ||||||
chr11:111841758
|
T | TAGAAATT others(332): Show |
1 | a0001c0001t0006g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1019-950_1019-949i others(341): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841758 | ||||||
chr11:111841967
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1019-1158C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841967 | ||||||
chr11:111842014
|
A | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0182 | 2 | NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1019-1205T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842014 | ||||||
chr11:111842034
|
T | C | 3 | a0001c0001t0003g0238a0001c0001t0003g0267a0001c0001t0008g0264 | 3 | NA18939.hp2 NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1019-1225A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842034 | ||||||
chr11:111842073
|
T | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1019-1264A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842073 | ||||||
chr11:111842219
|
A | C | 5 | a0002c0002t0001g0003a0002c0002t0001g0037a0002c0002t0001g0038others(2): Show | 6 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1019-1410T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842219 | ||||||
chr11:111842452
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1019-1643G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842452 | ||||||
chr11:111842595
|
A | G | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1019-1786T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842595 | ||||||
chr11:111842729
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1018+1872A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842729 | ||||||
chr11:111842865
|
A | G | 7 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0232others(4): Show | 7 | HG01123.hp2 HG01192.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1018+1736T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842865 | ||||||
chr11:111842905
|
C | T | 3 | a0001c0001t0018g0301a0001c0001t0018g0302a0001c0001t0029g0012 | 3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1018+1696G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842905 | ||||||
chr11:111842906
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1018+1695C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842906 | ||||||
chr11:111843005
|
G | A | 11 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(8): Show | 11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1018+1596C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111843005 | ||||||
chr11:111843536
|
T | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1018+1065A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111843536 | ||||||
chr11:111843979
|
T | C | 6 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018+622A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111843979 | ||||||
chr11:111844293
|
C | T | 4 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018+308G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111844293 | ||||||
chr11:111844360
|
T | C | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1018+241A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111844360 | ||||||
chr11:111844464
|
C | T | 1 | a0004c0004t0001g0097 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1018+137G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111844464 | ||||||
chr11:111844575
|
C | T | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0031g0109 | 3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1018+26G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111844575 | ||||||
chr11:111844755
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.896-32C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111844755 | ||||||
chr11:111844847
|
G | C | 79 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.896-124C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111844847 | ||||||
chr11:111844876
|
C | T | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.896-153G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111844876 | ||||||
chr11:111844992
|
C | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.896-269G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111844992 | ||||||
chr11:111845313
|
T | A | 1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.896-590A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845313 | ||||||
chr11:111845347
|
A | C | 209 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.896-624T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845347 | ||||||
chr11:111845427
|
G | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.896-704C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845427 | ||||||
chr11:111845639
|
G | C | 1 | a0001c0001t0002g0159 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.896-916C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845639 | ||||||
chr11:111845975
|
A | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0287a0001c0001t0001g0291others(13): Show | 16 | HG01952.hp1 HG02572.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.896-1252T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845975 | ||||||
chr11:111846052
|
C | T | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-1329G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846052 | ||||||
chr11:111846071
|
T | C | 1 | a0001c0001t0002g0180 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.896-1348A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846071 | ||||||
chr11:111846312
|
G | A | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.896-1589C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846312 | ||||||
chr11:111846590
|
A | C | 1 | a0001c0001t0003g0237 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.896-1867T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846590 | ||||||
chr11:111846599
|
G | A | 3 | a0001c0001t0009g0285a0005c0007t0009g0284a0005c0007t0009g0286 | 3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.896-1876C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846599 | ||||||
chr11:111846722
|
G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.896-1999C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846722 | ||||||
chr11:111846733
|
A | G | 1 | a0004c0004t0001g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.896-2010T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846733 | ||||||
chr11:111846737
|
G | C | 1 | a0002c0002t0004g0087 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.896-2014C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846737 | ||||||
chr11:111846935
|
G | T | 3 | a0001c0001t0002g0158a0001c0001t0002g0187a0001c0001t0002g0194 | 3 | NA18969.hp1 NA18983.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.896-2212C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846935 | ||||||
chr11:111847076
|
A | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-2353T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847076 | ||||||
chr11:111847130
|
A | T | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-2407T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847130 | ||||||
chr11:111847360
|
T | C | 3 | a0002c0002t0001g0058a0002c0002t0001g0060a0002c0002t0027g0059 | 3 | HG00544.hp1 HG02129.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.896-2637A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847360 | ||||||
chr11:111847490
|
C | T | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.896-2767G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847490 | ||||||
chr11:111847671
|
A | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-2948T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847671 | ||||||
chr11:111848045
|
C | T | 3 | a0002c0002t0001g0063a0002c0002t0001g0070a0002c0002t0001g0084 | 3 | NA18955.hp2 NA19005.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.896-3322G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848045 | ||||||
chr11:111848203
|
G | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-3480C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848203 | ||||||
chr11:111848405
|
T | C | 79 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.896-3682A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848405 | ||||||
chr11:111848450
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.896-3727A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848450 | ||||||
chr11:111848483
|
A | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-3760T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848483 | ||||||
chr11:111848540
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.896-3817T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848540 | ||||||
chr11:111848590
|
C | CA | 21 | a0001c0001t0002g0208a0001c0001t0003g0013a0001c0001t0003g0259others(18): Show | 22 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.896-3868dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848590 | ||||||
chr11:111848590
|
CA | C | 10 | a0001c0001t0002g0162a0002c0002t0001g0030a0002c0002t0004g0021others(7): Show | 10 | HG00621.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.896-3868delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848590 | ||||||
chr11:111848694
|
T | A | 76 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.896-3971A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848694 | ||||||
chr11:111848697
|
T | A | 2 | a0001c0001t0003g0213a0001c0001t0003g0276 | 2 | HG00558.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.896-3974A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848697 | ||||||
chr11:111848812
|
C | T | 5 | a0001c0001t0011g0129a0001c0001t0016g0127a0001c0001t0016g0128others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.896-4089G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848812 | ||||||
chr11:111848830
|
G | A | 5 | a0002c0002t0001g0015a0002c0002t0001g0029a0002c0002t0001g0033others(2): Show | 5 | HG00408.hp1 HG00609.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.896-4107C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848830 | ||||||
chr11:111848870
|
G | A | 226 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(223): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.896-4147C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848870 | ||||||
chr11:111848982
|
A | T | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.896-4259T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848982 | ||||||
chr11:111848999
|
A | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-4276T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848999 | ||||||
chr11:111849037
|
GTTTC | G | 60 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(57): Show | 64 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.896-4318_896-4315d others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849037 | ||||||
chr11:111849061
|
T | C | 13 | a0001c0001t0002g0130a0001c0001t0011g0129a0001c0001t0016g0127others(10): Show | 13 | HG00733.hp2 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.895+4319A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849061 | ||||||
chr11:111849090
|
G | A | 1 | a0002c0002t0004g0026 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.895+4290C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849090 | ||||||
chr11:111849201
|
C | T | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.895+4179G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849201 | ||||||
chr11:111849255
|
C | G | 1 | a0001c0001t0023g0269 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.895+4125G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849255 | ||||||
chr11:111849349
|
C | A | 128 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(125): Show | 133 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.895+4031G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849349 | ||||||
chr11:111849504
|
T | G | 4 | a0002c0002t0001g0028a0002c0002t0001g0062a0002c0002t0001g0067others(1): Show | 4 | NA18941.hp1 NA18979.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.895+3876A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849504 | ||||||
chr11:111849547
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.895+3833A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849547 | ||||||
chr11:111849638
|
C | G | 1 | a0001c0001t0003g0236 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.895+3742G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849638 | ||||||
chr11:111849960
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.895+3420G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849960 | ||||||
chr11:111849970
|
A | C | 1 | a0001c0001t0003g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.895+3410T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849970 | ||||||
chr11:111850162
|
T | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.895+3218A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850162 | ||||||
chr11:111850170
|
T | C | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0031g0109 | 3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.895+3210A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850170 | ||||||
chr11:111850222
|
G | C | 2 | a0002c0002t0004g0025a0002c0002t0004g0026 | 2 | NA18956.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.895+3158C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850222 | ||||||
chr11:111850585
|
T | C | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.895+2795A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850585 | ||||||
chr11:111850678
|
G | T | 1 | a0001c0001t0002g0130 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.895+2702C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850678 | ||||||
chr11:111850706
|
C | CAAAA | 65 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0210others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.895+2670_895+2673d others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAA | 8 | a0001c0001t0001g0212a0001c0001t0003g0232a0001c0001t0003g0260others(5): Show | 8 | HG00140.hp2 HG01358.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.895+2669_895+2673d others(7): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(1): Show |
82 | a0001c0001t0003g0217a0001c0001t0003g0218a0002c0002t0001g0001others(79): Show | 86 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.895+2666_895+2673d others(10): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(2): Show |
18 | a0001c0001t0003g0219a0002c0002t0001g0028a0002c0002t0001g0032others(15): Show | 18 | HG01192.hp1 HG01255.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.895+2665_895+2673d others(11): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(3): Show |
1 | a0002c0002t0021g0068 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.895+2664_895+2673d others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(7): Show |
6 | a0001c0001t0006g0143a0001c0001t0006g0144a0001c0001t0006g0145others(3): Show | 6 | HG02258.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+2660_895+2673d others(16): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0006g0142a0003c0003t0001g0123a0003c0003t0001g0124others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.895+2659_895+2673d others(17): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(9): Show |
1 | a0003c0003t0001g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.895+2658_895+2673d others(18): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(10): Show |
11 | a0001c0001t0004g0110a0001c0001t0005g0111a0001c0001t0005g0114others(8): Show | 11 | HG00738.hp1 HG01099.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.895+2657_895+2673d others(19): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(11): Show |
5 | a0001c0001t0001g0014a0001c0001t0005g0005a0001c0001t0005g0119others(2): Show | 6 | HG01123.hp1 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+2656_895+2673d others(20): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(12): Show |
5 | a0001c0001t0012g0196a0001c0001t0012g0197a0001c0001t0012g0199others(2): Show | 5 | HG02572.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(21): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(13): Show |
6 | a0001c0001t0001g0291a0001c0001t0005g0296a0001c0001t0005g0298others(3): Show | 6 | HG02809.hp1 HG02897.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(22): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(14): Show |
9 | a0001c0001t0001g0287a0001c0001t0001g0293a0001c0001t0002g0139others(6): Show | 9 | HG00741.hp1 HG01952.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(23): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(15): Show |
24 | a0001c0001t0001g0294a0001c0001t0002g0002a0001c0001t0002g0008others(21): Show | 27 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(24): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(16): Show |
15 | a0001c0001t0002g0009a0001c0001t0002g0135a0001c0001t0002g0156others(12): Show | 16 | HG00621.hp1 HG01255.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(25): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0002g0177 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.895+2673_895+2674i others(26): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(18): Show |
3 | a0001c0001t0002g0151a0001c0001t0002g0205a0001c0001t0016g0127 | 3 | HG02922.hp2 HG03669.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.895+2673_895+2674i others(27): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(19): Show |
7 | a0001c0001t0002g0152a0001c0001t0002g0154a0001c0001t0002g0178others(4): Show | 7 | HG02273.hp2 HG02630.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(28): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(20): Show |
10 | a0001c0001t0002g0155a0001c0001t0002g0182a0001c0001t0002g0183others(7): Show | 10 | HG00408.hp2 HG02135.hp1 HG04199.hp2 others(7): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(29): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0002g0150 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.895+2673_895+2674i others(30): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG02293.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.895+2673_895+2674i others(31): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(23): Show |
2 | a0001c0001t0002g0158a0001c0001t0002g0194 | 2 | NA18969.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.895+2673_895+2674i others(32): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850706
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.895+2673_895+2674i others(38): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | ||||||
chr11:111850893
|
C | T | 5 | a0002c0002t0001g0015a0002c0002t0001g0029a0002c0002t0001g0033others(2): Show | 5 | HG00408.hp1 HG00609.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.895+2487G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850893 | ||||||
chr11:111850940
|
T | G | 1 | a0001c0001t0012g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.895+2440A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850940 | ||||||
chr11:111850950
|
T | C | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.895+2430A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850950 | ||||||
chr11:111850957
|
C | T | 19 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(16): Show | 20 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.895+2423G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850957 | ||||||
chr11:111851062
|
C | G | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.895+2318G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851062 | ||||||
chr11:111851083
|
A | G | 1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.895+2297T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851083 | ||||||
chr11:111851116
|
A | G | 1 | a0002c0002t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.895+2264T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851116 | ||||||
chr11:111851180
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.895+2200T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851180 | ||||||
chr11:111851347
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.895+2033G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851347 | ||||||
chr11:111851477
|
C | CA | 21 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(18): Show | 22 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.895+1902dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851477 | ||||||
chr11:111851477
|
CA | C | 179 | a0001c0001t0001g0212a0001c0001t0001g0294a0001c0001t0002g0152others(176): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.895+1902delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851477 | ||||||
chr11:111851711
|
T | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.895+1669A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851711 | ||||||
chr11:111852108
|
G | C | 1 | a0001c0001t0002g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.895+1272C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852108 | ||||||
chr11:111852144
|
T | C | 1 | a0002c0002t0001g0069 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.895+1236A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852144 | ||||||
chr11:111852359
|
G | A | 1 | a0002c0002t0001g0070 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.895+1021C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852359 | ||||||
chr11:111852482
|
C | T | 8 | a0001c0001t0001g0212a0001c0001t0003g0211a0001c0001t0003g0221others(5): Show | 8 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.895+898G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852482 | ||||||
chr11:111852897
|
G | A | 2 | a0002c0002t0001g0071a0002c0002t0030g0082 | 2 | HG02602.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.895+483C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852897 | ||||||
chr11:111852939
|
C | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0277 | 2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.895+441G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852939 | ||||||
chr11:111852942
|
C | CA | 40 | a0001c0001t0001g0014a0001c0001t0001g0287a0001c0001t0001g0291others(37): Show | 41 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.895+437dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852942 | ||||||
chr11:111852942
|
C | CAA | 71 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(68): Show | 72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.895+436_895+437dup others(2): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852942 | ||||||
chr11:111852942
|
C | CAAA | 6 | a0001c0001t0001g0294a0001c0001t0003g0266a0001c0001t0003g0267others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+435_895+437dup others(3): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852942 | ||||||
chr11:111852960
|
T | A | 5 | a0001c0001t0011g0129a0001c0001t0016g0127a0001c0001t0016g0128others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.895+420A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852960 | ||||||
chr11:111852961
|
G | A | 1 | a0005c0007t0009g0286 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.895+419C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852961 | ||||||
chr11:111853058
|
A | G | 30 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(27): Show | 31 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.895+322T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111853058 | ||||||
chr11:111853080
|
TA | T | 128 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(125): Show | 133 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.895+299delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111853080 | ||||||
chr11:111853261
|
A | G | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0031g0109 | 3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.895+119T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111853261 | ||||||
chr11:111853540
|
G | A | 2 | a0002c0002t0001g0072a0002c0002t0001g0073 | 2 | NA18612.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.790-55C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 7/14 | chr11 | 111853540 | ||||||
chr11:111853605
|
T | C | 1 | a0002c0002t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.789+44A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 7/14 | chr11 | 111853605 | ||||||
chr11:111853609
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.789+40A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 7/14 | chr11 | 111853609 | ||||||
chr11:111853974
|
T | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.702-238A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111853974 | ||||||
chr11:111854023
|
C | G | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.702-287G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854023 | ||||||
chr11:111854095
|
C | CT | 90 | a0001c0001t0001g0212a0001c0001t0002g0135a0001c0001t0002g0147others(87): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.702-360dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854095 | ||||||
chr11:111854095
|
CT | C | 19 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(16): Show | 19 | HG01952.hp1 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.702-360delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854095 | ||||||
chr11:111854263
|
A | AT | 9 | a0001c0001t0001g0294a0001c0001t0002g0134a0001c0001t0002g0152others(6): Show | 9 | HG00738.hp2 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.702-528dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854263 | ||||||
chr11:111854263
|
AT | A | 135 | a0001c0001t0001g0014a0001c0001t0001g0287a0001c0001t0001g0291others(132): Show | 140 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.702-528delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854263 | ||||||
chr11:111854263
|
ATT | A | 10 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0232others(7): Show | 10 | HG01123.hp2 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.702-529_702-528del others(2): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854263 | ||||||
chr11:111854263
|
ATTT | A | 69 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.702-530_702-528del others(3): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854263 | ||||||
chr11:111854430
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.702-694G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854430 | ||||||
chr11:111854454
|
A | T | 1 | a0002c0002t0001g0027 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.702-718T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854454 | ||||||
chr11:111854562
|
C | T | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.702-826G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854562 | ||||||
chr11:111854564
|
C | T | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.702-828G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854564 | ||||||
chr11:111854871
|
C | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.702-1135G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854871 | ||||||
chr11:111854884
|
G | A | 1 | a0001c0001t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702-1148C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854884 | ||||||
chr11:111854958
|
C | T | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.702-1222G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854958 | ||||||
chr11:111855252
|
C | T | 1 | a0002c0002t0001g0081 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.702-1516G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855252 | ||||||
chr11:111855475
|
C | G | 1 | a0002c0002t0001g0028 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.702-1739G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855475 | ||||||
chr11:111855478
|
G | A | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.702-1742C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855478 | ||||||
chr11:111855530
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.702-1794T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855530 | ||||||
chr11:111855541
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.702-1805T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855541 | ||||||
chr11:111855544
|
G | A | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.702-1808C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855544 | ||||||
chr11:111855699
|
T | C | 1 | a0001c0001t0002g0192 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.701+1903A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855699 | ||||||
chr11:111855924
|
C | T | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.701+1678G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855924 | ||||||
chr11:111855956
|
C | T | 1 | a0001c0001t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.701+1646G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855956 | ||||||
chr11:111856075
|
G | A | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.701+1527C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856075 | ||||||
chr11:111856084
|
C | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.701+1518G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856084 | ||||||
chr11:111856220
|
T | C | 1 | a0001c0001t0015g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.701+1382A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856220 | ||||||
chr11:111856276
|
C | CA | 46 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(43): Show | 47 | HG00597.hp1 HG00597.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.701+1325dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856276 | ||||||
chr11:111856276
|
C | CAA | 8 | a0001c0001t0003g0270a0001c0001t0006g0142a0001c0001t0006g0143others(5): Show | 8 | HG00733.hp2 HG01099.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+1324_701+1325d others(4): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856276 | ||||||
chr11:111856289
|
A | AG | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0031g0109 | 3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.701+1312_701+1313i others(3): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856289 | ||||||
chr11:111856292
|
A | G | 1 | a0002c0002t0001g0027 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.701+1310T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856292 | ||||||
chr11:111856460
|
ATTTGT | A | 6 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.701+1137_701+1141d others(7): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856460 | ||||||
chr11:111856504
|
C | T | 231 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.701+1098G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856504 | ||||||
chr11:111856625
|
C | A | 13 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(10): Show | 14 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.701+977G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856625 | ||||||
chr11:111856625
|
C | CT | 9 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0005g0296others(6): Show | 9 | HG00609.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.701+976dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856625 | ||||||
chr11:111856625
|
CT | C | 8 | a0001c0001t0003g0225a0001c0001t0003g0271a0001c0001t0011g0129others(5): Show | 8 | HG01516.hp2 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+976delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856625 | ||||||
chr11:111856626
|
T | A | 1 | a0001c0001t0005g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.701+976A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856626 | ||||||
chr11:111856718
|
G | T | 1 | a0002c0002t0001g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.701+884C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856718 | ||||||
chr11:111856759
|
G | A | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.701+843C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856759 | ||||||
chr11:111856781
|
T | C | 19 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(16): Show | 20 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.701+821A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856781 | ||||||
chr11:111856824
|
G | A | 1 | a0001c0001t0002g0194 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.701+778C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856824 | ||||||
chr11:111856843
|
A | C | 2 | a0002c0002t0004g0025a0002c0002t0004g0026 | 2 | NA18956.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.701+759T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856843 | ||||||
chr11:111857035
|
A | C | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.701+567T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111857035 | ||||||
chr11:111857150
|
G | A | 12 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(9): Show | 12 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.701+452C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111857150 | ||||||
chr11:111857153
|
G | A | 1 | a0001c0001t0012g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.701+449C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111857153 | ||||||
chr11:111857829
|
T | C | 5 | a0001c0001t0003g0013a0001c0001t0003g0210a0001c0001t0003g0225others(2): Show | 5 | HG00140.hp1 HG01256.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-92A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111857829 | ||||||
chr11:111858084
|
G | A | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.566-347C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858084 | ||||||
chr11:111858121
|
G | C | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-384C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858121 | ||||||
chr11:111858188
|
A | G | 207 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(204): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.566-451T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858188 | ||||||
chr11:111858596
|
A | G | 2 | a0001c0001t0002g0201a0001c0001t0025g0133 | 2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.566-859T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858596 | ||||||
chr11:111858714
|
G | A | 1 | a0002c0002t0004g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.566-977C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858714 | ||||||
chr11:111858727
|
A | C | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.566-990T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858727 | ||||||
chr11:111858832
|
C | A | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.566-1095G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858832 | ||||||
chr11:111859042
|
C | T | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.566-1305G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859042 | ||||||
chr11:111859068
|
T | C | 6 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-1331A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859068 | ||||||
chr11:111859091
|
A | T | 3 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0010t0002g0206 | 3 | HG03669.hp1 NA20129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.566-1354T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859091 | ||||||
chr11:111859227
|
C | T | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.565+1320G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859227 | ||||||
chr11:111859267
|
A | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.565+1280T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859267 | ||||||
chr11:111859282
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+1265A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859282 | ||||||
chr11:111859497
|
CT | C | 207 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(204): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.565+1049delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859497 | ||||||
chr11:111859650
|
G | C | 1 | a0001c0001t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.565+897C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859650 | ||||||
chr11:111859850
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.565+697T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859850 | ||||||
chr11:111860063
|
T | C | 1 | a0001c0001t0012g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.565+484A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111860063 | ||||||
chr11:111860283
|
C | T | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.565+264G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111860283 | ||||||
chr11:111860817
|
G | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.477-182C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111860817 | ||||||
chr11:111860852
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.477-217A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111860852 | ||||||
chr11:111860887
|
T | C | 2 | a0001c0001t0015g0146a0001c0001t0015g0203 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.477-252A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111860887 | ||||||
chr11:111860983
|
G | A | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.477-348C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111860983 | ||||||
chr11:111861250
|
T | G | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.477-615A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861250 | ||||||
chr11:111861492
|
T | C | 76 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.477-857A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861492 | ||||||
chr11:111861549
|
G | A | 1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.477-914C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861549 | ||||||
chr11:111861566
|
T | C | 6 | a0002c0002t0004g0101a0002c0002t0004g0102a0002c0002t0004g0103others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-931A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861566 | ||||||
chr11:111861579
|
C | G | 1 | a0001c0001t0024g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.477-944G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861579 | ||||||
chr11:111861886
|
G | A | 1 | a0002c0002t0001g0081 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.477-1251C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861886 | ||||||
chr11:111861912
|
T | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.477-1277A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861912 | ||||||
chr11:111862137
|
A | G | 1 | a0002c0002t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.477-1502T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862137 | ||||||
chr11:111862239
|
C | CT | 9 | a0001c0001t0002g0147a0001c0001t0010g0288a0001c0001t0010g0289others(6): Show | 9 | HG02145.hp2 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.477-1605dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862239 | ||||||
chr11:111862352
|
A | G | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.477-1717T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862352 | ||||||
chr11:111862523
|
C | T | 5 | a0001c0001t0003g0013a0001c0001t0003g0210a0001c0001t0003g0225others(2): Show | 5 | HG00140.hp1 HG01256.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.477-1888G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862523 | ||||||
chr11:111862584
|
T | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.477-1949A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862584 | ||||||
chr11:111862814
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.477-2179C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862814 | ||||||
chr11:111862863
|
T | C | 5 | a0001c0001t0001g0293a0001c0001t0006g0142a0001c0001t0006g0143others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.477-2228A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862863 | ||||||
chr11:111862894
|
G | A | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.477-2259C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862894 | ||||||
chr11:111863090
|
G | A | 1 | a0002c0002t0030g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.476+2091C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863090 | ||||||
chr11:111863190
|
C | T | 5 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219others(2): Show | 5 | HG01255.hp1 HG01884.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+1991G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863190 | ||||||
chr11:111863374
|
T | A | 79 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.476+1807A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863374 | ||||||
chr11:111863420
|
C | T | 291 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(288): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.476+1761G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863420 | ||||||
chr11:111863441
|
T | C | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.476+1740A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863441 | ||||||
chr11:111863467
|
G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.476+1714C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863467 | ||||||
chr11:111863568
|
G | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.476+1613C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863568 | ||||||
chr11:111863686
|
G | C | 1 | a0002c0002t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.476+1495C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863686 | ||||||
chr11:111863713
|
T | C | 1 | a0002c0002t0001g0084 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.476+1468A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863713 | ||||||
chr11:111863855
|
G | A | 1 | a0001c0001t0017g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.476+1326C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863855 | ||||||
chr11:111863893
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.476+1288T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863893 | ||||||
chr11:111863980
|
C | A | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0031g0109 | 3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.476+1201G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863980 | ||||||
chr11:111864121
|
C | T | 80 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(77): Show | 84 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.476+1060G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864121 | ||||||
chr11:111864149
|
A | G | 1 | a0002c0002t0002g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.476+1032T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864149 | ||||||
chr11:111864272
|
G | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.476+909C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864272 | ||||||
chr11:111864589
|
G | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.476+592C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864589 | ||||||
chr11:111864673
|
A | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.476+508T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864673 | ||||||
chr11:111864692
|
T | C | 1 | a0001c0001t0003g0278 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.476+489A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864692 | ||||||
chr11:111864771
|
T | A | 1 | a0001c0001t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.476+410A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864771 | ||||||
chr11:111865072
|
C | T | 1 | a0001c0001t0003g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.476+109G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111865072 | ||||||
chr11:111865258
|
G | A | 1 | a0001c0001t0003g0273 | 1 | NA20805.hp1 | splice_region_variant&intron_variant | LOW | c.406-7C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111865258 | ||||||
chr11:111865297
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.406-46A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111865297 | ||||||
chr11:111865859
|
ATGTGGCT | A | 11 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0293others(8): Show | 11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.406-615_406-609del others(7): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111865859 | ||||||
chr11:111866093
|
G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.406-842C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866093 | ||||||
chr11:111866161
|
G | A | 1 | a0002c0002t0004g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.406-910C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866161 | ||||||
chr11:111866206
|
G | A | 226 | a0001c0001t0001g0014a0001c0001t0001g0212a0001c0001t0001g0287others(223): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.406-955C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866206 | ||||||
chr11:111866241
|
G | C | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.406-990C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866241 | ||||||
chr11:111866289
|
C | T | 19 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(16): Show | 20 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.406-1038G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866289 | ||||||
chr11:111866365
|
C | T | 1 | a0001c0001t0019g0220 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.406-1114G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866365 | ||||||
chr11:111866588
|
A | G | 1 | a0001c0001t0003g0276 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.406-1337T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866588 | ||||||
chr11:111866721
|
C | G | 15 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(12): Show | 16 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.406-1470G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866721 | ||||||
chr11:111866733
|
A | C | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.406-1482T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866733 | ||||||
chr11:111866764
|
C | T | 3 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219 | 3 | HG01255.hp1 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.406-1513G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866764 | ||||||
chr11:111866858
|
C | G | 1 | a0002c0002t0001g0088 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.406-1607G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866858 | ||||||
chr11:111866956
|
G | A | 4 | a0001c0001t0006g0142a0001c0001t0006g0143a0001c0001t0006g0144others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+1646C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866956 | ||||||
chr11:111867044
|
G | A | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.405+1558C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867044 | ||||||
chr11:111867079
|
A | G | 2 | a0001c0001t0003g0215a0001c0001t0008g0216 | 2 | NA18965.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.405+1523T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867079 | ||||||
chr11:111867090
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.405+1512C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867090 | ||||||
chr11:111867108
|
A | C | 5 | a0003c0003t0001g0123a0003c0003t0001g0124a0003c0003t0001g0125others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+1494T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867108 | ||||||
chr11:111867189
|
C | T | 79 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.405+1413G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867189 | ||||||
chr11:111867218
|
G | A | 1 | a0001c0001t0015g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.405+1384C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867218 | ||||||
chr11:111867263
|
A | C | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.405+1339T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867263 | ||||||
chr11:111867445
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.405+1157G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867445 | ||||||
chr11:111867508
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.405+1094T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867508 | ||||||
chr11:111867543
|
A | G | 1 | a0002c0002t0004g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.405+1059T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867543 | ||||||
chr11:111867742
|
T | C | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.405+860A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867742 | ||||||
chr11:111867920
|
C | T | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.405+682G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867920 | ||||||
chr11:111868200
|
T | C | 1 | a0001c0001t0003g0274 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.405+402A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111868200 | ||||||
chr11:111868465
|
T | C | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+137A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111868465 | ||||||
chr11:111868485
|
T | C | 14 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(11): Show | 15 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.405+117A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111868485 | ||||||
chr11:111868594
|
G | T | 1 | a0002c0002t0001g0003 | 2 | HG01257.hp1 HG01258.hp2 |
splice_region_variant&intron_variant | LOW | c.405+8C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111868594 | ||||||
chr11:111868816
|
C | T | 14 | a0001c0001t0004g0110a0001c0001t0005g0005a0001c0001t0005g0111others(11): Show | 15 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-80G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111868816 | ||||||
chr11:111868831
|
C | T | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271-95G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111868831 | ||||||
chr11:111868930
|
G | T | 1 | a0001c0001t0003g0214 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.271-194C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111868930 | ||||||
chr11:111869074
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.271-338T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869074 | ||||||
chr11:111869411
|
TAC | T | 3 | a0001c0001t0020g0107a0001c0001t0020g0108a0001c0001t0031g0109 | 3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.271-677_271-676del others(2): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869411 | ||||||
chr11:111869766
|
T | C | 58 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(55): Show | 62 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.270+466A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869766 | ||||||
chr11:111869870
|
GGT | G | 10 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0003g0292others(7): Show | 10 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+360_270+361del others(2): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869870 | ||||||
chr11:111869880
|
C | T | 1 | a0002c0002t0004g0021 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.270+352G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869880 | ||||||
chr11:111870001
|
G | A | 2 | a0001c0001t0012g0196a0001c0001t0012g0197 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.270+231C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111870001 | ||||||
chr11:111870103
|
T | G | 1 | a0001c0001t0005g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.270+129A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111870103 | ||||||
chr11:111870137
|
G | A | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.270+95C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111870137 | ||||||
chr11:111870381
|
G | GC | 72 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.132-12dupG | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870381 | ||||||
chr11:111870382
|
C | CA | 33 | a0001c0001t0001g0014a0001c0001t0001g0294a0001c0001t0002g0201others(30): Show | 33 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.132-13dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870382 | ||||||
chr11:111870382
|
C | CCA | 4 | a0001c0001t0003g0276a0001c0001t0003g0277a0001c0001t0003g0278others(1): Show | 4 | HG01109.hp2 NA18951.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.132-13_132-12insTG | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870382 | ||||||
chr11:111870387
|
A | C | 3 | a0001c0001t0001g0212a0001c0001t0003g0210a0001c0001t0003g0211 | 3 | HG00140.hp1 HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.132-17T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870387 | ||||||
chr11:111870420
|
C | T | 6 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0017others(3): Show | 6 | HG00609.hp1 NA18946.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-50G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870420 | ||||||
chr11:111870607
|
T | G | 6 | a0002c0002t0004g0101a0002c0002t0004g0102a0002c0002t0004g0103others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-237A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870607 | ||||||
chr11:111870740
|
T | C | 79 | a0001c0001t0001g0212a0001c0001t0003g0010a0001c0001t0003g0013others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.132-370A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870740 | ||||||
chr11:111870746
|
C | T | 98 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(95): Show | 102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.132-376G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870746 | ||||||
chr11:111870909
|
T | C | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG00597.hp2 NA18977.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+443A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870909 | ||||||
chr11:111870973
|
G | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0287a0001c0001t0001g0291others(13): Show | 16 | HG01952.hp1 HG02572.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.131+379C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870973 | ||||||
chr11:111871040
|
C | A | 1 | a0002c0002t0001g0295 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.131+312G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871040 | ||||||
chr11:111871087
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.131+265C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871087 | ||||||
chr11:111871167
|
G | C | 4 | a0001c0001t0005g0296a0001c0001t0005g0297a0001c0001t0005g0298others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.131+185C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871167 | ||||||
chr11:111871244
|
G | A | 1 | a0002c0002t0004g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.131+108C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871244 | ||||||
chr11:111871245
|
T | G | 2 | a0001c0001t0018g0301a0001c0001t0018g0302 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.131+107A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871245 | ||||||
chr11:111871310
|
G | T | 1 | a0001c0001t0003g0013 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.131+42C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871310 | ||||||
chr11:111871317
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131+35G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871317 | ||||||
chr11:111871347
|
C | T | 1 | a0002c0002t0021g0011 | 1 | NA18978.hp1 | splice_region_variant&intron_variant | LOW | c.131+5G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871347 |